Vascular endothelial cell development and diversity
Open accessAbstract
Vascular endothelial cells form the inner layer of blood vessels where they have a key role in the development and maintenance of the functional circulatory system and provide paracrine support to surrounding non-vascular cells. Technical advances in the past 5 years in single-cell genomics and in in vivo genetic labelling have facilitated greater insights into endothelial cell development, plasticity and heterogeneity. These advances have also contributed to a new understanding of the timing of endothelial cell subtype differentiation and its relationship to the cell cycle. Identification of novel tissue-specific gene expression patterns in endothelial cells has led to the discovery of crucial signalling pathways and new interactions with other cell types that have key roles in both tissue maintenance and disease pathology. In this Review, we describe the latest findings in vascular endothelial cell development and diversity, which are often supported by large-scale, single-cell studies, and discuss the implications of these findings for vascular medicine. In addition, we highlight how techniques such as single-cell multimodal omics, which have become increasingly sophisticated over the past 2 years, are being utilized to study normal vascular physiology as well as functional perturbations in disease.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In disease states, most transcriptional changes occur within capillary beds and alveolar specialization is diminished in lung adenocarcinoma.
“In disease states, most transcriptional changes have been found to occur within capillary beds and in consistent, the alveolar specialization is diminished in lung adenocarcinoma9,10”
From Endothelial Pim3 kinase protects the vascular barrier during lung metastasis (2024) · cites this paper as [10]
In “Organ-specific findings at high resolution” (page not provided), the review reports that capillary endothelial cells had the most potentially pathological transcriptional changes in a comparison of bronchopulmonary dysplasia samples. It also reports loss of specialized aerocyte capillaries and emergence of an intermediate capillary population in a human lung adenocarcinoma sample. The claim extends the finding about where most changes occur beyond the specific disease comparison described. (LLM, conf=0.85)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Single-cell transcriptomics of 20 mouse organs creates a Tabula Muris
The Tabula Muris Consortium, coordination, O., coordination, L., processing, O. C. A., sequencing, L. P. A., analysis, C. D., annotation, C. T., Writing group, Supplemental text writing group, & Principal investigators (2018) · Nature · doi:10.1038/s41586-018-0590-4 · Cited by 3,326 · see citing works
Simultaneous epitope and transcriptome measurement in single cells
Stoeckius, M., Hafemeister, C., Stephenson, W., Houck-Loomis, B., Chattopadhyay, P. K., Swerdlow, H., Satija, R., & Smibert, P. (2017) · Nature Methods · doi:10.1038/nmeth.4380 · Cited by 3,098 · see citing works
Pericytes regulate the blood–brain barrier
Armulik, A., Genové, G., Mäe, M., Nisancioglu, M. H., Wallgard, E., Niaudet, C., He, L., Norlin, J., Lindblom, P., Strittmatter, K., et al. (2010) · Nature · doi:10.1038/nature09522 · Cited by 2,843 · see citing works
VEGF in signaling and disease: beyond discovery and development
Apte, R. S., Chen, D. S., & Ferrara, N. (2019) · Cell · doi:10.1016/j.cell.2019.01.021 · Cited by 2,721 · see citing works
Vascularized and functional human liver from an iPSC-derived organ bud transplant
Takebe, T., Sekine, K., Enomura, M., Koike, H., Kimura, M., Ogaeri, T., Zhang, R.-R., Ueno, Y., Zheng, Y.-W., Koike, N., et al. (2013) · Nature · doi:10.1038/nature12271 · Cited by 2,170 · see citing works
Pericytes are required for blood–brain barrier integrity during embryogenesis
Daneman, R., Zhou, L., Kebede, A. A., & Barres, B. A. (2010) · Nature · doi:10.1038/nature09513 · Cited by 2,128 · see citing works
A molecular atlas of cell types and zonation in the brain vasculature
Vanlandewijck, M., He, L., Mäe, M. A., Andrae, J., Ando, K., Del Gaudio, F., Nahar, K., Lebouvier, T., Laviña, B., Gouveia, L., et al. (2018) · Nature · doi:10.1038/nature25739 · Cited by 2,074 · see citing works
Dll4 signalling through Notch1 regulates formation of tip cells during angiogenesis
Hellström, M., Phng, L.-K., Hofmann, J. J., Wallgard, E., Coultas, L., Lindblom, P., Alva, J., Nilsson, A.-K., Karlsson, L., Gaiano, N., et al. (2007) · Nature · doi:10.1038/nature05571 · Cited by 1,775 · see citing works
Cells of the adult human heart
Litviňuková, M., Talavera-López, C., Maatz, H., Reichart, D., Worth, C. L., Lindberg, E. L., Kanda, M., Polanski, K., Heinig, M., Lee, M., et al. (2020) · Nature · doi:10.1038/s41586-020-2797-4 · Cited by 1,729 · see citing works
A molecular cell atlas of the human lung from single-cell RNA sequencing
Travaglini, K. J., Nabhan, A. N., Penland, L., Sinha, R., Gillich, A., Sit, R. V., Chang, S., Conley, S. D., Mori, Y., Seita, J., et al. (2020) · Nature · doi:10.1038/s41586-020-2922-4 · Cited by 1,657 · see citing works
Mapping the Mouse Cell Atlas by Microwell-Seq
Han, X., Wang, R., Zhou, Y., Fei, L., Sun, H., Lai, S., Saadatpour, A., Zhou, Z., Chen, H., Ye, F., et al. (2018) · Cell · doi:10.1016/j.cell.2018.02.001 · Cited by 1,597 · see citing works
Single cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations
MacParland, S. A., Liu, J. C., Ma, X.-Z., Innes, B. T., Bartczak, A. M., Gage, B. K., Manuel, J., Khuu, N., Echeverri, J., Linares, I., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06318-7 · Cited by 1,552 · see citing works
Single-Cell Transcriptome Atlas of Murine Endothelial Cells
Kalucka, J. M., de Rooij, L. P. M. H., Goveia, J., Rohlenová, K., Dumas, S. J., Meta, E., Conchinha, N. V., Taverna, F., Teuwen, L.-A. M. N., Veys, K., et al. (2020) · Cell · doi:10.1016/j.cell.2020.01.015 · Cited by 1,362 · see citing works
Phenotypic Heterogeneity of the Endothelium
Aird, W. C. (2007) · Circulation Research · doi:10.1161/01.res.0000255690.03436.ae · Cited by 1,252 · see citing works
An in vivo model of functional and vascularized human brain organoids
Mansour, A. A., Gonçalves, J. T., Bloyd, C. W., Li, H., Fernandes, S., Quang, D., Johnston, S., Parylak, S. L., Jin, X., & Gage, F. H. (2018) · Nature Biotechnology · doi:10.1038/nbt.4127 · Cited by 1,211 · see citing works
A human liver cell atlas reveals heterogeneity and epithelial progenitors
Aizarani, N., Saviano, A., Sagar, Mailly, L., Durand, S., Herman, J. S., Pessaux, P., Baumert, T. F., & Grün, D. (2019) · Nature · doi:10.1038/s41586-019-1373-2 · Cited by 1,147 · see citing works
Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease
Park, J., Shrestha, R., Qiu, C., Kondo, A., Huang, S., Werth, M., Li, M., Barasch, J., & Suszták, K. (2018) · Science · doi:10.1126/science.aar2131 · Cited by 1,065 · see citing works
Yang, C., Zhao, H., Bruzzone, L., Benediktsson, J. A., Liang, Y., Liu, B., Zeng, X., Guan, R., Li, C., & Ouyang, Z. (2020) · Nature Communications · doi:10.1038/s41467-020-20215-y · Cited by 1,065 · see citing works
The Tabula Sapiens: A multiple-organ, single-cell transcriptomic atlas of humans
The Tabula Sapiens Consortium*, Jones, R. C., Karkanias, J., Krasnow, M. A., Pisco, A. O., Quake, S. R., Salzman, J., Yosef, N., Bulthaup, B., Brown, P., et al. (2022) · Science · doi:10.1126/science.abl4896 · Cited by 1,056 · see citing works
Self-citationBlockade of Dll4 inhibits tumour growth by promoting non-productive angiogenesis
Noguera‐Troise, I., Daly, C., Papadopoulos, N. J., Coetzee, S., Boland, P., Gale, N. W., Lin, H. C., Yancopoulos, G. D., & Thurston, G. (2006) · Nature · doi:10.1038/nature05355 · Cited by 1,032 · see citing works
Biomanufacturing of organ-specific tissues with high cellular density and embedded vascular channels
Skylar‐Scott, M. A., Uzel, S. G. M., Nam, L. L., Ahrens, J. H., Truby, R. L., Damaraju, S., & Lewis, J. A. (2019) · Science Advances · doi:10.1126/sciadv.aaw2459 · Cited by 953 · see citing works
Flow-enhanced vascularization and maturation of kidney organoids in vitro
Homan, K. A., Gupta, N., Kroll, K. T., Kolesky, D. B., Skylar-Scott, M., Miyoshi, T., Mau, D., Valerius, M. T., Ferrante, T., Bonventre, J. V., et al. (2019) · Nature Methods · doi:10.1038/s41592-019-0325-y · Cited by 939 · see citing works
The bone marrow microenvironment at single-cell resolution
Tikhonova, A. N., Dolgalev, I., Hu, H., Sivaraj, K. K., Hoxha, E., Cuesta-Domínguez, Á., Pinho, S., Akhmetzyanova, I., Gao, J., Witkowski, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1104-8 · Cited by 936 · see citing works
Self-Renewing Resident Cardiac Macrophages Limit Adverse Remodeling Following Myocardial Infarction
Dick, S. A., Macklin, J. A., Nejat, S., Momen, A., Clemente-Casares, X., Althagafi, M. G., Chen, J., Kantores, C., Hosseinzadeh, S., Aronoff, L., et al. (2019) · Nature Immunology · doi:10.1038/s41590-018-0272-2 · Cited by 883 · see citing works
Angiogenesis: A Team Effort Coordinated by Notch
Phng, L., & Gerhardt, H. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.01.015 · Cited by 834 · see citing works
Lawson, N. D., Vogel, A. M., & Weinstein, B. M. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00198-3 · Cited by 813 · see citing works
Suchting, S., Freitas, C., le Noble, F. A. C., Benedito, R., Bréant, C., Duarte, A., & Eichmann, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611177104 · Cited by 812 · see citing works
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets
Delorey, T. M., Ziegler, C. G. K., Heimberg, G., Normand, R., Yang, Y., Segerstolpe, Å., Abbondanza, D., Fleming, S. J., Subramanian, A., Montoro, D. T., et al. (2021) · Nature · doi:10.1038/s41586-021-03570-8 · Cited by 809 · see citing works
Human blood vessel organoids as a model of diabetic vasculopathy
Wimmer, R. A., Leopoldi, A., Aichinger, M., Wick, N., Hantusch, B., Novatchkova, M., Taubenschmid, J., Hämmerle, M., Esk, C., Bagley, J. A., et al. (2019) · Nature · doi:10.1038/s41586-018-0858-8 · Cited by 803 · see citing works
A human brain vascular atlas reveals diverse mediators of Alzheimer’s risk
Yang, A. C., Vest, R. T., Kern, F., Lee, D. P., Agam, M., Maat, C. A., Losada, P. M., Chen, M. B., Schaum, N., Khoury, N., et al. (2022) · Nature · doi:10.1038/s41586-021-04369-3 · Cited by 797 · see citing works
Delta-like ligand 4 (Dll4) is induced by VEGF as a negative regulator of angiogenic sprouting
Lobov, I. B., Renard, R. A., Papadopoulos, N., Gale, N. W., Thurston, G., Yancopoulos, G. D., & Wiegand, S. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611206104 · Cited by 775 · see citing works
A human cell atlas of fetal gene expression
Cao, J., O’Day, D. R., Pliner, H. A., Kingsley, P. D., Deng, M., Daza, R. M., Zager, M. A., Aldinger, K. A., Blecher-Gonen, R., Zhang, F., et al. (2020) · Science · doi:10.1126/science.aba7721 · Cited by 764 · see citing works
Organotypic vasculature: From descriptive heterogeneity to functional pathophysiology
Augustin, H. G., & Koh, G. Y. (2017) · Science · doi:10.1126/science.aal2379 · Cited by 762 · see citing works
Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors
Young, M. D., Mitchell, T. J., Vieira Braga, F. A., Tran, M. G. B., Stewart, B. J., Ferdinand, J. R., Collord, G., Botting, R. A., Popescu, D.-M., Loudon, K. W., et al. (2018) · Science · doi:10.1126/science.aat1699 · Cited by 762 · see citing works
A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility
Cusanovich, D. A., Hill, A. J., Aghamirzaie, D., Daza, R. M., Pliner, H. A., Berletch, J. B., Filippova, G. N., Huang, X., Christiansen, L., DeWitt, W. S., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.052 · Cited by 759 · see citing works
Lineage tracing on transcriptional landscapes links state to fate during differentiation
Weinreb, C., Rodriguez-Fraticelli, A., Camargo, F. D., & Klein, A. M. (2020) · Science · doi:10.1126/science.aaw3381 · Cited by 730 · see citing works
Campisi, M., Shin, Y., Osaki, T., Hajal, C., Chiono, V., & Kamm, R. D. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.07.014 · Cited by 718 · see citing works
Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity
You, L., Lin, F., Lee, C. T., DeMayo, F. J., Tsai, M., & Tsai, S. Y. (2005) · Nature · doi:10.1038/nature03511 · Cited by 664 · see citing works
VEGF and Notch in Tip and Stalk Cell SelectionPreprint
Blanco, R. E., & Gerhardt, H. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006569 · Cited by 622 · see citing works
Nolan, D. J., Ginsberg, M. D., Israely, E., Palikuqi, B., Poulos, M. G., James, D., Ding, B., Schachterle, W., Liu, Y., Rosenwaks, Z., et al. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.06.017 · Cited by 603 · see citing works
Cardioids reveal self-organizing principles of human cardiogenesis
Hofbauer, P., Jahnel, S. M., Papai, N., Giesshammer, M., Deyett, A., Schmidt, C., Penc, M., Tavernini, K., Grdseloff, N., Meledeth, C., et al. (2021) · Cell · doi:10.1016/j.cell.2021.04.034 · Cited by 588 · see citing works
Synthesis-on-substrate of quantum dot solids
Jiang, Y., Sun, C., Xu, J., Li, S., Cui, M., Fu, X., Liu, Y., Liu, Y., Wan, H., Wei, K., et al. (2022) · Nature · doi:10.1038/s41586-022-05486-3 · Cited by 586 · see citing works
Coronary arteries form by developmental reprogramming of venous cells
Red‐Horse, K., Ueno, H., Weissman, I. L., & Krasnow, M. A. (2010) · Nature · doi:10.1038/nature08873 · Cited by 539 · see citing works
Self-citationLewis-Israeli, Y. R., Wasserman, A. H., Gabalski, M. A., Volmert, B. D., Ming, Y., Ball, K. A., Yang, W., Zou, J., Ni, G., Pajares, N., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25329-5 · Cited by 536 · see citing works
Endothelium structure and function in kidney health and disease
Jourde‐Chiche, N., Fakhouri, F., Dou, L., Bellien, J., Burtey, S., Frimat, M., Jarrot, P., Kaplanski, G., Quintrec, M. L., Pernin, V., et al. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-018-0098-z · Cited by 499 · see citing works
Capillary cell-type specialization in the alveolus
Gillich, A., Zhang, F., Farmer, C. G., Travaglini, K. J., Tan, S. Y., Gu, M., Zhou, B., Feinstein, J. A., Krasnow, M. A., & Metzger, R. J. (2020) · Nature · doi:10.1038/s41586-020-2822-7 · Cited by 490 · see citing works
Single-Cell Transcriptome Analysis Maps the Developmental Track of the Human Heart
Cui, Y., Zheng, Y., Liu, X., Yan, L., Fan, X., Yong, J., Hu, Y., Dong, J., Li, Q., Wu, X., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.01.079 · Cited by 478 · see citing works
Muto, Y., Wilson, P. C., Ledru, N., Wu, H., Dimke, H., Waikar, S. S., & Humphreys, B. D. (2021) · Nature Communications · doi:10.1038/s41467-021-22368-w · Cited by 460 · see citing works
Integrated Single-Cell Atlas of Endothelial Cells of the Human Lung
Schupp, J. C., Adams, T. S., Cosme, C., Raredon, M. S. B., Yuan, Y., Omote, N., Poli, S., Chioccioli, M., Rose, K.-A., Manning, E. P., et al. (2021) · Circulation · doi:10.1161/circulationaha.120.052318 · Cited by 453 · see citing works
Human heart-forming organoids recapitulate early heart and foregut development
Drakhlis, L., Biswanath, S., Farr, C.-M., Lupanow, V., Teske, J., Ritzenhoff, K., Franke, A., Manstein, F., Bolesani, E., Kempf, H., et al. (2021) · Nature Biotechnology · doi:10.1038/s41587-021-00815-9 · Cited by 452 · see citing works
The molecular basis of endothelial cell plasticity
Dejana, E., Hirschi, K. K., & Simons, M. (2017) · Nature Communications · doi:10.1038/ncomms14361 · Cited by 441 · see citing works
van den Berg, C. W., Ritsma, L., Avramut, M. C., Wiersma, L. E., van den Berg, B. M., Leuning, D. G., Lievers, E., Koning, M., Vanslambrouck, J. M., Koster, A. J., et al. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.01.041 · Cited by 417 · see citing works
Endothelial signalling by the Notch ligand Delta-like 4 restricts angiogenesis
Leslie, J. D., Ariza‐McNaughton, L., Bermange, A. L., Mcadow, R., Johnson, S. L., & Lewis, J. H. (2007) · Development · doi:10.1242/dev.003244 · Cited by 415 · see citing works
Single-cell RNA sequencing of mouse brain and lung vascular and vessel-associated cell types
He, L., Vanlandewijck, M., Mäe, M. A., Andrae, J., Ando, K., Del Gaudio, F., Nahar, K., Lebouvier, T., Laviña, B., Gouveia, L., et al. (2018) · Scientific Data · doi:10.1038/sdata.2018.160 · Cited by 413 · see citing works
Massive and Reproducible Production of Liver Buds Entirely from Human Pluripotent Stem Cells
Takebe, T., Sekine, K., Kimura, M., Yoshizawa, E., Ayano, S., Koido, M., Funayama, S., Nakanishi, N., Hisai, T., Kobayashi, T., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.005 · Cited by 407 · see citing works
Dll4 and Notch signalling couples sprouting angiogenesis and artery formation
Pitulescu, M. E., Schmidt, I., Giaimo, B. D., Antoine, T., Berkenfeld, F., Ferrante, F., Park, H., Ehling, M., Biljes, D., Rocha, S. F., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3555 · Cited by 397 · see citing works
Wu, B., Zhang, Z., Lui, W., Chen, X., Wang, Y., Chamberlain, A. A., Moreno‐Rodriguez, R. A., Markwald, R. R., O'Rourke, B. P., Sharp, D. J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.10.023 · Cited by 394 · see citing works
Single-cell multimodal omics: the power of many
Zhu, C., Preissl, S., & Ren, B. (2020) · Nature Methods · doi:10.1038/s41592-019-0691-5 · Cited by 386 · see citing works
A human cell atlas of fetal chromatin accessibility
Domcke, S., Hill, A. J., Daza, R. M., Cao, J., O’Day, D. R., Pliner, H. A., Aldinger, K. A., Pokholok, D., Zhang, F., Milbank, J. H., et al. (2020) · Science · doi:10.1126/science.aba7612 · Cited by 375 · see citing works
Paired-cell sequencing enables spatial gene expression mapping of liver endothelial cells
Halpern, K. B., Shenhav, R., Massalha, H., Toth, B., Egozi, A., Massasa, E. E., Medgalia, C., David, E., Giladi, A., Moor, A. E., et al. (2018) · Nature Biotechnology · doi:10.1038/nbt.4231 · Cited by 368 · see citing works
Rethinking organoid technology through bioengineering
Garreta, E., Kamm, R. D., Lopes, S. M. C. D. S., Lancaster, M. A., Weiss, R., Trepat, X., Hyun, I., & Montserrat, N. (2020) · Nature Materials · doi:10.1038/s41563-020-00804-4 · Cited by 326 · see citing works
A single-cell atlas of the normal and malformed human brain vasculature
Winkler, E. A., Kim, C. N., Ross, J. M., Garcia, J. H., Gil, E., Oh, I., Chen, L. Q., Wu, D., Catapano, J. S., Raygor, K. P., et al. (2022) · Science · doi:10.1126/science.abi7377 · Cited by 324 · see citing works
Single-cell dissection of the human brain vasculature
García, F., Sun, N., Lee, H., Godlewski, B. R., Mathys, H., Galani, K., Zhou, B., Jiang, X., Ng, A. P., Mantero, J. C., et al. (2022) · Nature · doi:10.1038/s41586-022-04521-7 · Cited by 310 · see citing works
Single-cell RNA sequencing in cardiovascular development, disease and medicine
Paik, D. T., Cho, S., Tian, L., Chang, H. Y., & Wu, J. C. (2020) · Nature Reviews Cardiology · doi:10.1038/s41569-020-0359-y · Cited by 306 · see citing works
Dynamic Endothelial Cell Rearrangements Drive Developmental Vessel Regression
Franco, C. A., Jones, M. L., Bernabéu, M. O., Geudens, I., Mathivet, T., Rosa, A., Lopes, F. M., Lima, A. P., Ragab, A., Collins, R., et al. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002125 · Cited by 296 · see citing works
Paik, D. T., Tian, L., Williams, I. M., Rhee, S., Zhang, H., Liu, C., Mishra, R., Wu, S. M., Red‐Horse, K., & Wu, J. C. (2020) · Circulation · doi:10.1161/circulationaha.119.041433 · Cited by 282 · see citing works
Self-citationShear-induced Notch-Cx37-p27 axis arrests endothelial cell cycle to enable arterial specification
Fang, J. S., Coon, B. G., Gillis, N. E., Chen, Z., Qiu, J., Chittenden, T. W., Burt, J. M., Schwartz, M. A., & Hirschi, K. K. (2017) · Nature Communications · doi:10.1038/s41467-017-01742-7 · Cited by 281 · see citing works
Mapping human haematopoietic stem cells from haemogenic endothelium to birth
Calvanese, V., Capellera-Garcia, S., Ma, F., Fares, I., Liebscher, S., Ng, E. S., Ekstrand, S., Aguadé-Gorgorió, J., Vavilina, A., Lefaudeux, D., et al. (2022) · Nature · doi:10.1038/s41586-022-04571-x · Cited by 265 · see citing works
Covassin, L., Villefranc, J. A., Kacergis, M. C., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506886103 · Cited by 263 · see citing works
Classifying Drosophila Olfactory Projection Neuron Subtypes by Single-Cell RNA Sequencing
Li, H., Horns, F., Wu, B., Xie, Q., Li, J., Li, T., Luginbuhl, D. J., Quake, S. R., & Luo, L. (2017) · Cell · doi:10.1016/j.cell.2017.10.019 · Cited by 256 · see citing works
Transcriptional and epigenomic landscapes of CNS and non-CNS vascular endothelial cells
Sabbagh, M. F., Heng, J. S., Luo, C., Castanon, R. G., Nery, J. R., Rattner, A., Goff, L. A., Ecker, J. R., & Nathans, J. (2018) · eLife · doi:10.7554/elife.36187 · Cited by 245 · see citing works
Characterization of the COPD alveolar niche using single-cell RNA sequencing
Sauler, M., McDonough, J. E., Adams, T. S., Kothapalli, N., Bärnthaler, T., Werder, R. B., Schupp, J. C., Nouws, J., Robertson, M. J., Coarfa, C., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28062-9 · Cited by 240 · see citing works
The sinus venosus contributes to coronary vasculature through VEGFC-stimulated angiogenesis
Chen, H. I., Sharma, B., Akerberg, B. N., Nurmi, H. J., Kivelä, R., Saharinen, P., Aghajanian, H. K., McKay, A. S., Bogard, P. E., Chang, A. H., et al. (2014) · Development · doi:10.1242/dev.113639 · Cited by 234 · see citing works
Self-citationEpithelial Vegfa Specifies a Distinct Endothelial Population in the Mouse Lung
Ellis, L. V., Cain, M. P., Hutchison, V., Flodby, P., Crandall, E. D., Borok, Z., Zhou, B., Ostrin, E. J., Wythe, J. D., & Chen, J. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.01.009 · Cited by 234 · see citing works
Defining the role of pulmonary endothelial cell heterogeneity in the response to acute lung injury
Niethamer, T. K., Stabler, C. T., Leach, J. P., Zepp, J. A., Morley, M. P., Babu, A., Zhou, S., & Morrisey, E. E. (2020) · eLife · doi:10.7554/elife.53072 · Cited by 234 · see citing works
Brain Endothelial Cells Are Exquisite Sensors of Age-Related Circulatory Cues
Chen, M. B., Yang, A. C., Yousef, H., Lee, D., Chen, W., Schaum, N., Lehallier, B., Quake, S. R., & Wyss-Coray, T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.03.012 · Cited by 233 · see citing works
Single-cell analysis of early progenitor cells that build coronary arteries
Su, T., Stanley, G., Sinha, R., D’Amato, G., Das, S., Rhee, S., Chang, A. H., Poduri, A., Raftrey, B. C., Dinh, T. T., et al. (2018) · Nature · doi:10.1038/s41586-018-0288-7 · Cited by 230 · see citing works
Self-citationArteries are formed by vein-derived endothelial tip cells
Xu, C., Hasan, S. S., Schmidt, I., Rocha, S. F., Pitulescu, M. E., Bussmann, J., Meyen, D., Raz, E., Adams, R. H., & Siekmann, A. F. (2014) · Nature Communications · doi:10.1038/ncomms6758 · Cited by 225 · see citing works
Notch controls retinal blood vessel maturation and quiescence
Ehling, M., Adams, S., Benedito, R., & Adams, R. H. (2013) · Development · doi:10.1242/dev.093351 · Cited by 223 · see citing works
Su, T., Yang, Y., Lai, S., Jeong, J., Jung, Y., McConnell, M., Utsumi, T., & Iwakiri, Y. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2020.12.007 · Cited by 220 · see citing works
A Unique Collateral Artery Development Program Promotes Neonatal Heart Regeneration
Das, S., Goldstone, A. B., Wang, H., Farry, J. M., D’Amato, G., Paulsen, M. J., Eskandari, A., Hironaka, C. E., Phansalkar, R., Sharma, B., et al. (2019) · Cell · doi:10.1016/j.cell.2018.12.023 · Cited by 219 · see citing works
Self-citationDe novo formation of a distinct coronary vascular population in neonatal heart
Tian, X., Hu, T., Zhang, H., He, L., Huang, X., Liu, Q., Yu, W., He, L., Yang, X. Y., Yan, Y., et al. (2014) · Science · doi:10.1126/science.1251487 · Cited by 216 · see citing works
Large‐scale identification of genes implicated in kidney glomerulus development and function
Takemoto, M., He, L., Norlin, J., Patrakka, J., Xiao, Z., Petrova, T. V., Bondjers, C., Asp, J., Wallgard, E., Sun, Y., et al. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601014 · Cited by 216 · see citing works
A molecular cell atlas of the human lung from single cell RNA sequencingPreprint
Travaglini, K. J., Nabhan, A. N., Penland, L., Sinha, R., Gillich, A., Sit, R. V., Chang, S., Conley, S. D., Mori, Y., Seita, J., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/742320 · Cited by 216 · see citing works
Fu, J., Akat, K. M., Sun, Z., Zhang, W., Schlöndorff, D., Liu, Z., Tuschl, T., Lee, K., & He, C. (2019) · Journal of the American Society of Nephrology · doi:10.1681/asn.2018090896 · Cited by 215 · see citing works
McCracken, I. R., Saginc, G., He, L., Huseynov, A., Daniels, A., Fletcher, S., Peghaire, C. R., Kalna, V., Mäe, M. A., Muhl, L., et al. (2021) · Circulation · doi:10.1161/circulationaha.120.052824 · Cited by 212 · see citing works
Single cell transcriptomic analysis of murine lung development on hyperoxia-induced damage
Hurskainen, M., Mižíková, I., Cook, D. P., Andersson, N., Cyr-Depauw, C., Lesage, F., Helle, E., Renesme, L., Jankov, R. P., Heikinheimo, M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21865-2 · Cited by 212 · see citing works
Miao, Z., Balzer, M. S., Ma, Z., Liu, H., Wu, J., Shrestha, R., Arányi, T., Kwan, A., Kondo, A., Pontoglio, M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22266-1 · Cited by 209 · see citing works
Bussmann, J., Wolfe, S. A., & Siekmann, A. F. (2011) · Development · doi:10.1242/dev.059881 · Cited by 208 · see citing works
Single-Cell Analysis of Blood-Brain Barrier Response to Pericyte Loss
Mäe, M. A., He, L., Nordling, S., Vázquez-Liébanas, E., Nahar, K., Jung, B., Li, X., Tan, B. C., Foo, J. C., Cazenave‐Gassiot, A., et al. (2020) · Circulation Research · doi:10.1161/circresaha.120.317473 · Cited by 203 · see citing works
Guo, M., Du, Y., Gokey, J. J., Ray, S., Bell, S. M., Adam, M., Sudha, P., Perl, A. T., Deshmukh, H. S., Potter, S. S., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07770-1 · Cited by 201 · see citing works
Role of Venous Endothelial Cells in Developmental and Pathologic Angiogenesis
Lee, H., Xu, Y., He, L., Choi, W., Gonzalez, D. G., Jin, S., & Simons, M. (2021) · Circulation · doi:10.1161/circulationaha.121.054071 · Cited by 199 · see citing works
Engineering Vascularized Organoid-on-a-Chip Models
Shirure, V. S., Hughes, C. C. W., & George, S. C. (2021) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-090120-094330 · Cited by 197 · see citing works
Jin, Y., Muhl, L., Burmakin, M., Wang, Y., Duchez, A., Betsholtz, C., Arthur, H. M., & Jakobsson, L. (2017) · Nature Cell Biology · doi:10.1038/ncb3534 · Cited by 193 · see citing works
A single-cell transcriptomic landscape of the lungs of patients with COVID-19
Wang, S., Yao, X., Ma, S., Ping, Y., Fan, Y., Sun, S., He, Z., Shi, Y., Sun, L., Xiao, S., et al. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00796-6 · Cited by 191 · see citing works
Chung, J.-J., Goldstein, L. D., Chen, Y.-J. J., Lee, J., Webster, J. D., Roose‐Girma, M., Paudyal, S. C., Modrusan, Z. D., Dey, A., & Shaw, A. S. (2020) · Journal of the American Society of Nephrology · doi:10.1681/asn.2020020220 · Cited by 189 · see citing works
McDonald, A. I., Shirali, A. S., Aragón, R. L., Ma, F., Hernandez, G. E., Vaughn, D. A., Mack, J. J., Lim, T. Y., Sunshine, H., Zhao, P., et al. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.07.011 · Cited by 187 · see citing works
Dumas, S. J., Meta, E., Borri, M., Goveia, J., Rohlenová, K., Conchinha, N. V., Falkenberg, K. D., Teuwen, L.-A. M. N., de Rooij, L. P. M. H., Kalucka, J. M., et al. (2019) · Journal of the American Society of Nephrology · doi:10.1681/asn.2019080832 · Cited by 184 · see citing works
Genomic, epigenomic, and biophysical cues controlling the emergence of the lung alveolus
Zepp, J. A., Morley, M. P., Loebel, C., Kremp, M. M., Chaudhry, F. N., Basil, M. C., Leach, J. P., Liberti, D. C., Niethamer, T. K., Ying, Y., et al. (2021) · Science · doi:10.1126/science.abc3172 · Cited by 184 · see citing works
Single-cell atlases: shared and tissue-specific cell types across human organs
Elmentaite, R., Conde, C. D., Yang, L., & Teichmann, S. A. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00449-w · Cited by 171 · see citing works
A Single-Cell Transcriptome Atlas of the Mouse Glomerulus
Karaiskos, N., Rahmatollahi, M., Boltengagen, A., Liu, H., Hoehne, M., Rinschen, M. M., Schermer, B., Benzing, T. R., Rajewsky, N., Kocks, C., et al. (2018) · Journal of the American Society of Nephrology · doi:10.1681/asn.2018030238 · Cited by 166 · see citing works
The molecular regulation of arteriovenous specification and maintenance
Fish, J. E., & Wythe, J. D. (2015) · Developmental Dynamics · doi:10.1002/dvdy.24252 · Cited by 164 · see citing works
Single-cell transcriptomics reveals gene expression dynamics of human fetal kidney development
Hochane, M., van den Berg, P. R., Fan, X., Bérenger-Currias, N. M. L. P., Adegeest, E., Bialecka, M., Nieveen, M. C., Menschaart, M., Lopes, S. M. C. D. S., & Semrau, S. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000152 · Cited by 160 · see citing works
A single-cell atlas of mouse lung development
Negretti, N. M., Plosa, E. J., Benjamin, J. T., Schuler, B. A., Habermann, A. C., Jetter, C. S., Gulleman, P. M., Bunn, C., Hackett, A. N., Ransom, M. A., et al. (2021) · Development · doi:10.1242/dev.199512 · Cited by 157 · see citing works
Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney
Menon, R., Otto, E. A., Kokoruda, A., Zhou, J., Zhang, Z., Yoon, E., Chen, Y., Troyanskaya, O. G., Spence, J. R., Kretzler, M., et al. (2018) · Development · doi:10.1242/dev.164038 · Cited by 155 · see citing works
Franco, C. A., Jones, M. L., Bernabéu, M. O., Vion, A.-C., Barbacena, P., Fan, J., Mathivet, T., Fonseca, C. G., Ragab, A., Yamaguchi, T. P., et al. (2016) · eLife · doi:10.7554/elife.07727 · Cited by 154 · see citing works
Endothelial Notch signalling limits angiogenesis via control of artery formation
Hasan, S. S., Tsaryk, R., Lange, M., Wisniewski, L., Moore, J. C., Lawson, N. D., Wojciechowska, K., Schnittler, H., & Siekmann, A. F. (2017) · Nature Cell Biology · doi:10.1038/ncb3574 · Cited by 154 · see citing works
Modulation of VEGF signalling output by the Notch pathway
Siekmann, A. F., Covassin, L., & Lawson, N. D. (2008) · BioEssays · doi:10.1002/bies.20736 · Cited by 152 · see citing works
Endocardium Minimally Contributes to Coronary Endothelium in the Embryonic Ventricular Free Walls
Zhang, H., Pu, W., Li, G., Huang, X., He, L., Tian, X., Liu, Q., Zhang, L., Wu, S. M., Sucov, H. M., et al. (2016) · Circulation Research · doi:10.1161/circresaha.116.308749 · Cited by 149 · see citing works
Arterialization requires the timely suppression of cell growth
Luo, W., García-Gónzalez, I., Fernández-Chacón, M., Casquero-García, V., Sanchez-Muñoz, M. S., Mühleder, S., García-Ortega, L., Andrade, J., Potente, M., & Benedito, R. (2020) · Nature · doi:10.1038/s41586-020-3018-x · Cited by 139 · see citing works
Arterial and Venous Progenitors of the Major Axial Vessels Originate at Distinct Locations
Kohli, V., Schumacher, J. A., Desai, S. P., et al. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.03.017 · Cited by 134 · see citing works
Bahary, N., Goishi, K., Stuckenholz, C., Weber, G., LeBlanc, J., Schafer, C. A., Berman, S. S., Klagsbrun, M., & Zon, L. I. (2007) · Blood · doi:10.1182/blood-2006-04-016378 · Cited by 132 · see citing works
In vivo modulation of endothelial polarization by Apelin receptor signalling
Kwon, H.-B., Wang, S., Helker, C. S., Rasouli, S. J., Maischein, H., Offermanns, S., Herzog, W., & Stainier, D. Y. R. (2016) · Nature Communications · doi:10.1038/ncomms11805 · Cited by 132 · see citing works
Hupe, M., Li, M. X., Kneitz, S., Davydova, D., Yokota, C., Kele, J., Hot, B., Stenman, J. M., & Gessler, M. (2017) · Science Signaling · doi:10.1126/scisignal.aag2476 · Cited by 129 · see citing works
A molecular map of murine lymph node blood vascular endothelium at single cell resolution
Brulois, K., Rajaraman, A., Szade, A., Nordling, S., Bogoslowski, A., Đermadi, D., Rahman, M., Kiefel, H., O’Hara, E., Koning, J. J., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17291-5 · Cited by 128 · see citing works
Self-citationNotch as a hub for signaling in angiogenesis
Benedito, R., & Hellström, M. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.01.010 · Cited by 127 · see citing works
Differentiation of Human Intestinal Organoids with Endogenous Vascular Endothelial Cells
Holloway, E. M., Wu, J. H., Czerwinski, M. J., Sweet, C. W., Wu, A., Tsai, Y.-H., Huang, S., Stoddard, A. E., Capeling, M. M., Glass, I. A., et al. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.07.023 · Cited by 125 · see citing works
Zarkada, G., Howard, J. P., Xiao, X., Park, H., Bizou, M., Leclerc, S., Künzel, S. E., Boisseau, B., Li, J., Cagnone, G., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.06.021 · Cited by 123 · see citing works
Sharma, B., Ho, L., Ford, G. H., Chen, H. I., Goldstone, A. B., Woo, Y.-P. J., Quertermous, T., Reversade, B., & Red‐Horse, K. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.08.008 · Cited by 121 · see citing works
Self-citationZhao, L., Li, Z., Vong, J. S. L., Chen, X., Lai, H. M., Yan, L. Y. C., Huang, J., Sy, S. K. H., Tian, X. Y., Huang, Y., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18249-3 · Cited by 119 · see citing works
Distinct Notch signaling outputs pattern the developing arterial system
Quillien, A., Moore, J. C., Shin, M., et al. (2014) · Development · doi:10.1242/dev.099986 · Cited by 117 · see citing works
High mitogenic stimulation arrests angiogenesis
Pontes-Quero, S., Fernández-Chacón, M., Luo, W., Lunella, F. F., Casquero-García, V., García-Gónzalez, I., Hermoso, A., Rocha, S. F., Bansal, M., & Benedito, R. (2019) · Nature Communications · doi:10.1038/s41467-019-09875-7 · Cited by 114 · see citing works
Inverso, D., Shi, J., Lee, K. H., Jakab, M., Ben-Moshe, S., Kulkarni, S. R., Schneider, M., Wang, G., Komeili, M., Vélez, P. A., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.05.001 · Cited by 114 · see citing works
Direct retrieval of isoprene from satellite-based infrared measurements
Fu, D., Millet, D. B., Wells, K. C., Payne, V. H., Yu, S., Guenther, A., & Eldering, A. (2019) · Nature Communications · doi:10.1038/s41467-019-11835-0 · Cited by 112 · see citing works
Signaling Pathways in the Specification of Arteries and Veins
Corada, M., Morini, M. F., & Dejana, E. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.303218 · Cited by 111 · see citing works
Alk1 controls arterial endothelial cell migration in lumenized vessels
Rochon, E. R., Menon, P. G., & Roman, B. L. (2016) · Development · doi:10.1242/dev.135392 · Cited by 111 · see citing works
VEGF-B Promotes Endocardium-Derived Coronary Vessel Development and Cardiac Regeneration
Ramste, M. O., Sultan, I., Paech, J., Hemanthakumar, K. A., Yu, W., He, L., Tang, J., Sun, Y., Hlushchuk, R., Huan, X., et al. (2020) · Circulation · doi:10.1161/circulationaha.120.050635 · Cited by 109 · see citing works
Park, H., Furtado, J., Poulet, M., Chung, M., Yun, S., Lee, S., Sessa, W. C., Franco, C. A., Schwartz, M. A., & Eichmann, A. (2021) · Circulation · doi:10.1161/circulationaha.120.053047 · Cited by 108 · see citing works
ALK1 signaling in development and disease: new paradigms
Roman, B. L., & Hinck, A. P. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2636-4 · Cited by 103 · see citing works
Chang, A. H., Raftrey, B. C., D’Amato, G., Surya, V. N., Poduri, A., Chen, H. I., Goldstone, A. B., Woo, Y.-P. J., Fuller, G. G., Dunn, A. R., et al. (2017) · Genes & Development · doi:10.1101/gad.301549.117 · Cited by 97 · see citing works
Self-citationFeng, W. H., Chen, L., Nguyen, P. K. P., Wu, S. M., & Li, G. (2019) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2019.00165 · Cited by 97 · see citing works
Cross-platform single cell analysis of kidney development shows stromal cells express Gdnf
Magella, B., Adam, M., Potter, A., Venkatasubramanian, M., Chetal, K., Hay, S. B., Salomonis, N., & Potter, S. S. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.11.006 · Cited by 89 · see citing works
Weijts, B. G. M. W., Gutierrez, E., Saikin, S. K., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07732-7 · Cited by 89 · see citing works
Poduri, A., Chang, A. H., Raftrey, B. C., Rhee, S., Van, M. V., & Red‐Horse, K. (2017) · Development · doi:10.1242/dev.150904 · Cited by 88 · see citing works
Self-citationAng, L. T., Nguyen, A. T., Liu, K. J., Chen, A. C., Xiong, X., Curtis, M. B., Martin, R. M., Raftry, B. C., Ng, C., Vogel, U., et al. (2022) · Cell · doi:10.1016/j.cell.2022.05.024 · Cited by 88 · see citing works
Self-citationMadéo, J., Man, M. K. L., Sahoo, C., et al. (2020) · Institutional Repositories DataBase (IRDB) · Cited by 87 · see citing works
Blockade of Dll4 Inhibits Tumour Growth by Promoting Non‐Productive Angiogenesis
Noguera‐Troise, I., Daly, C., Papadopoulos, N. J., et al. (2007) · Novartis Foundation symposium · doi:10.1002/9780470319413.ch9 · Cited by 86 · see citing works
Veins and Arteries Build Hierarchical Branching Patterns Differently: Bottom‐Up versus Top‐Down
Red‐Horse, K., & Siekmann, A. F. (2019) · BioEssays · doi:10.1002/bies.201800198 · Cited by 86 · see citing works
Self-citationEndothelial Cell Development and Its Application to Regenerative Medicine
Qiu, J., & Hirschi, K. K. (2019) · Circulation Research · doi:10.1161/circresaha.119.311405 · Cited by 84 · see citing works
Endothelial cell cycle state determines propensity for arterial-venous fate
Chavkin, N. W., Genet, G., Poulet, M., Jeffery, E. D., Marziano, C., Genet, N., Vasavada, H. H., Nelson, E. A., Acharya, B. R., Kour, A., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33324-7 · Cited by 83 · see citing works
Hou, S., Li, Z., Dong, J., Gao, Y., Chang, Z., Ding, X., Li, S., Li, Y., Zeng, Y., Qian, X., et al. (2022) · Cell Research · doi:10.1038/s41422-022-00615-z · Cited by 81 · see citing works
Gómez-Salinero, J. M., Izzo, F., Lin, Y., Houghton, S., Itkin, T., Geng, F., Bram, Y., Adelson, R. P., Lu, T. M., Inghirami, G., et al. (2022) · Cell stem cell · doi:10.1016/j.stem.2022.03.002 · Cited by 80 · see citing works
BMP10-mediated ALK1 signaling is continuously required for vascular development and maintenance
Capasso, T. L., Li, B., Volek, H. J., Khalid, W., Rochon, E. R., Anbalagan, A., Herdman, C., Yost, H. J., Villanueva, F. S., Kim, K., et al. (2019) · Angiogenesis · doi:10.1007/s10456-019-09701-0 · Cited by 77 · see citing works
Vegf signaling promotes vascular endothelial differentiation by modulating etv2 expression
Casie Chetty, S., Rost, M. S., Enriquez, J. R., Schumacher, J. A., Baltrunaite, K., Rossi, A., Stainier, D. Y. R., & Sumanas, S. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.03.005 · Cited by 76 · see citing works
Shi, W., Sheng, X., Dorr, K. M., Hutton, J. E., Emerson, J. I., Davies, H. A., Andrade, T. D., Wasson, L. K., Greco, T. M., Hashimoto, Y., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.09.022 · Cited by 75 · see citing works
Activation of Smad2/3 signaling by low fluid shear stress mediates artery inward remodeling
Deng, H., Min, E., Baeyens, N., Coon, B. G., Hu, R., Zhuang, Z. W., Chen, M., Huang, B., Afolabi, T., Zarkada, G., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2105339118 · Cited by 74 · see citing works
Venous identity requires BMP signalling through ALK3
Neal, A., Nornes, S., Payne, S., Wallace, M. D., Fritzsche, M., Louphrasitthiphol, P., Wilkinson, R. N., Chouliaras, K. M., Liu, K., Plant, K., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08315-w · Cited by 68 · see citing works
McCracken, I. R., Dobie, R., Bennett, M., Passi, R., Beqqali, A., Henderson, N. C., Mountford, J. C., Riley, P. R., Ponting, C. P., Smart, N., et al. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac023 · Cited by 67 · see citing works
Sissaoui, S., Yu, J., Yan, A.-M., Li, R., Yukselen, O., Kucukural, A., Zhu, L., & Lawson, N. (2020) · Circulation Research · doi:10.1161/circresaha.119.316075 · Cited by 66 · see citing works
MLL-AF9 initiates transformation from fast-proliferating myeloid progenitors
Chen, X., Burkhardt, D. B., Hartman, A. A., Hu, X., Eastman, A. E., Sun, C., Wang, X., Zhong, M., Krishnaswamy, S., & Guo, S. (2019) · Nature Communications · doi:10.1038/s41467-019-13666-5 · Cited by 58 · see citing works
Vela pulsar wind nebula X-rays are polarized to near the synchrotron limit
Xie, F., Marco, A. D., Monaca, F. L., et al. (2022) · Nature · doi:10.1038/s41586-022-05476-5 · Cited by 58 · see citing works
D’Amato, G., Phansalkar, R., Naftaly, J. A., Fan, X., Amir, Z. A., Coronado, P. E. R., Cowley, D. O., Quinn, K. E., Sharma, B., Caron, K. M., et al. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.10.007 · Cited by 51 · see citing works
Self-citationDach1 Extends Artery Networks and Protects Against Cardiac Injury
Raftrey, B. C., Williams, I. M., Coronado, P. E. R., Fan, X., Chang, A. H., Zhao, M., Roth, R., Trimm, E., Racelis, R., D’Amato, G., et al. (2021) · Circulation Research · doi:10.1161/circresaha.120.318271 · Cited by 50 · see citing works
Self-citationA specialized bone marrow microenvironment for fetal haematopoiesis
Liu, Y., Chen, Q., Jeong, H., Koh, B. I., Watson, E. C., Xu, C., Stehling, M., Zhou, B., & Adams, R. H. (2022) · Nature Communications · doi:10.1038/s41467-022-28775-x · Cited by 50 · see citing works
Geudens, I., Coxam, B., Alt, S., et al. (2019) · Development · doi:10.1242/dev.181024 · Cited by 48 · see citing works
A circular white-light flare with impulsive and gradual white-light kernels
Hao, Q., Yang, K., Cheng, X., Guo, Y., Fang, C., Ding, M. D., Chen, P. F., & Li, Z. (2017) · Nature Communications · doi:10.1038/s41467-017-02343-0 · Cited by 43 · see citing works
Cardioids reveal self-organizing principles of human cardiogenesisPreprint
Hofbauer, P., Jahnel, S. M., Pápai, N., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.06.189431 · Cited by 43 · see citing works
Phansalkar, R., Krieger, J., Zhao, M., Kolluru, S. S., Jones, R. C., Quake, S. R., Weissman, I. L., Bernstein, D., Winn, V. D., D’Amato, G., et al. (2021) · eLife · doi:10.7554/elife.70246 · Cited by 42 · see citing works
Self-citationEffects of fetal exposure to nicotine on dental development of the laboratory rat
Chowdhury, I., & Bromage, T. G. (2000) · The Anatomical Record · doi:10.1002/(sici)1097-0185(20000401)258:4 · Cited by 40 · see citing works
Perinatal angiogenesis from pre-existing coronary vessels via DLL4–NOTCH1 signalling
Lu, P., Wang, Y., Liu, Y., et al. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00747-1 · Cited by 39 · see citing works
Gene Expression Programs of Mouse Endothelial Cells in Kidney Development and Disease
Brunskill, E. W., & Potter, S. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012034 · Cited by 37 · see citing works
Aging of the Vascular System and Neural Diseases
Watanabe, C., Imaizumi, T., Kawai, H., Suda, K., Honma, Y., Ichihashi, M., Ema, M., & Mizutani, K. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.557384 · Cited by 34 · see citing works
Cardiac endothelial cells maintain open chromatin and expression of cardiomyocyte myofibrillar genes
Yucel, N. D., Axsom, J., Yang, Y., Li, L., Rhoades, J. H., & Arany, Z. P. (2020) · eLife · doi:10.7554/elife.55730 · Cited by 34 · see citing works
MEKK3–TGFβ crosstalk regulates inward arterial remodeling
Deng, H., Xu, Y., Hu, X., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2112625118 · Cited by 34 · see citing works
Integrated Single Cell Atlas of Endothelial Cells of the Human LungPreprint
Schupp, J. C., Adams, T. S., Cosme, C., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.21.347914 · Cited by 32 · see citing works
den Braanker, H., van Stigt, A. C., Kok, M. R., Lubberts, E., & Bisoendial, R. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111976 · Cited by 32 · see citing works
WASp controls oriented migration of endothelial cells to achieve functional vascular patterning
Rosa, A., Giese, W., Meier, K., et al. (2021) · Development · doi:10.1242/dev.200195 · Cited by 32 · see citing works
Endothelial cell biology of Endoglin in hereditary hemorrhagic telangiectasia
Sugden, W. W., & Siekmann, A. F. (2018) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000419 · Cited by 29 · see citing works
Extension of Endocardium-Derived Vessels Generate Coronary Arteries in Neonates
Tang, J., Zhu, H., Tian, X., Wang, H., Liu, S., Liu, K., Zhao, H., He, L., Huang, X., Feng, Z., et al. (2022) · Circulation Research · doi:10.1161/circresaha.121.320335 · Cited by 28 · see citing works
Brain endothelial cells are exquisite sensors of age-related circulatory cuesPreprint
Chen, M. B., Yousef, H., Yang, A. C., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/617258 · Cited by 25 · see citing works
Su, T., Yang, Y., Lai, S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.18.997452 · Cited by 25 · see citing works
Payne, S., Gunadasa-Rohling, M., Neal, A., Redpath, A. N., Patel, J., Chouliaras, K. M., Ratnayaka, I., Smart, N., & Val, S. D. (2019) · Nature Communications · doi:10.1038/s41467-019-10710-2 · Cited by 24 · see citing works
AI-empowered integrative structural characterization of m6A methyltransferase complex
Yan, X., Pei, K., Guan, Z., et al. (2022) · Cell Research · doi:10.1038/s41422-022-00741-8 · Cited by 24 · see citing works
Li, Z., Solomonidis, E. G., Berkeley, B., Tang, M. N. H., Stewart, K. R., Perez-Vicencio, D., McCracken, I. R., Spiroski, A., Gray, G. A., Barton, A. K., et al. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac151 · Cited by 23 · see citing works
Bagarinao, E., Watanabe, H., Maesawa, S., Mori, D., Hara, K., Kawabata, K., Yoneyama, N., Ohdake, R., Imai, K., Masuda, M., et al. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.592469 · Cited by 19 · see citing works
Zygmunt, T., Trzaska, S., Edelstein, L., et al. (2012) · Journal of Cell Science · doi:10.1242/jcs.108555 · Cited by 18 · see citing works
Jiang, Z. Y., Lu, Z., Kou, S., et al. (2020) · Cell Research · doi:10.1038/s41422-020-00436-y · Cited by 17 · see citing works
Epithelial Vegfa specifies a distinct endothelial population in the mouse lungPreprint
Ellis, L. V., Cain, M. P., Hutchison, V., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/840033 · Cited by 16 · see citing works
Neal, A., Nornes, S., Louphrasitthiphol, P., Sacilotto, N., Preston, M. D., Fleisinger, L., Payne, S., & Val, S. D. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.01.002 · Cited by 13 · see citing works
Bais, A. S., Cerqueira, D. M., Clugston, A. S., Bodnar, A. J., Ho, J., & Kostka, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-01790-6 · Cited by 13 · see citing works
Peng, X., Emiliani, F. E., Smallwood, P. M., et al. (2018) · eLife · doi:10.7554/elife.40982 · Cited by 11 · see citing works
Differentiation of human intestinal organoids with endogenous vascular endothelial cellsPreprint
Holloway, E. M., Wu, J. H., Czerwinkski, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.15.991950 · Cited by 10 · see citing works
Endothelial Cell Cycle State Determines Propensity for Arterial-Venous FatePreprint
Chavkin, N. W., Genet, G., Poulet, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.12.246512 · Cited by 9 · see citing works
Identification of evolutionary trajectories shared across human betacoronavirusesPreprint
Escalera‐Zamudio, M., Pond, S. L. K., de la Viña, N. M., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.24.445313 · Cited by 7 · see citing works
Wasp controls oriented migration of endothelial cells to achieve functional vascular patterningPreprint
Rosa, A., Giese, W., Meier, K., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.15.296574 · Cited by 4 · see citing works
Gutierrez, M. E. C., Hill, M. C., Largoza, G. E., Martin, J. F., & Wythe, J. D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.15.468651 · Cited by 4 · see citing works
Publisher Correction: High mitogenic stimulation arrests angiogenesis
Pontes-Quero, S., Fernández-Chacón, M., Luo, W., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10474-9 · Cited by 3 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Endothelial cell metabolism in cardiovascular physiology and disease
Pasut, A., Lama, E., Van Craenenbroeck, A. H., Kroon, J., & Carmeliet, P. (2025) · Nature Reviews Cardiology · doi:10.1038/s41569-025-01162-x · Cited by 74 · see citing works
Endothelial Pim3 kinase protects the vascular barrier during lung metastasis
Santio, N. M., Ganesh, K., Kaipainen, P. P., Halme, A., Seyednasrollah, F., Arbash, E., Hänninen, S., Kivelä, R., Carpen, O., & Saharinen, P. (2024) · Nature Communications · doi:10.1038/s41467-024-54445-1 · Cited by 9 · see citing works
- Authors
- Trimm, E., & Red-Horse, K.
- Affiliations
- Stanford Medicine (US)
- ORCID
- Trimm, Emily
- Venue
- Nature Reviews Cardiology
- Published
- 2022-10-05
- Volume
- 20
- Issue
- 3
- Pages
- 197-210
- ISSN
- 1759-5002 (ISSN-L)
- 1759-5010
- PMC
- PMC9533272
- OpenAlex
- W4301600652
- Cited by
- 537
- References
- 187
- Citations by year
- 2026: 143 · 2025: 196 · 2024: 162 · 2023: 34 · 2022: 2
- FWCI
- 10.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Nature Reviews Cardiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Hertz Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- vascular endothelial cells, endothelial cell development, endothelial heterogeneity, endothelial plasticity, endothelial differentiation, cell cycle, tissue-specific gene expression, single-cell RNA sequencing, brain endothelium, lung endothelium, liver endothelium
- MeSH terms
- Cell Differentiation, Humans, Signal Transduction, Endothelial Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review