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Bioengineering Approaches for the Advanced Organoid Research
Open accessAbstract
Recent advances in 3D cell culture technology have enabled scientists to generate stem cell derived organoids that recapitulate the structural and functional characteristics of native organs. Current organoid technologies have been striding toward identifying the essential factors for controlling the processes involved in organoid development, including physical cues and biochemical signaling. There is a growing demand for engineering dynamic niches characterized by conditions that resemble in vivo organogenesis to generate reproducible and reliable organoids for various applications. Innovative biomaterial‐based and advanced engineering‐based approaches have been incorporated into conventional organoid culture methods to facilitate the development of organoid research. The recent advances in organoid engineering, including extracellular matrices and genetic modulation, are comprehensively summarized to pinpoint the parameters critical for organ‐specific patterning. Moreover, perspective trends in developing tunable organoids in response to exogenous and endogenous cues are discussed for next‐generation developmental studies, disease modeling, and therapeutics.
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“However, organoid cultures exhibit significant heterogeneity, variable complexity in cellular composition, can undergo poorly-controlled morphogenesis in self-assembly process, and often lack stromal, vascular and immunological components4,13.”
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“However, organoid cultures exhibit significant heterogeneity, variable complexity in cellular composition, can undergo poorly-controlled morphogenesis in self-assembly process, and often lack stromal, vascular and immunological components4,13.”
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“However, organoid cultures exhibit significant heterogeneity, variable complexity in cellular composition, can undergo poorly-controlled morphogenesis in self-assembly process, and often lack stromal, vascular and immunological components4,13.”
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Cites
Takahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673
Genome engineering using the CRISPR-Cas9 system
Ran, F. A., Hsu, P. D., Wright, J., Agarwala, V., Scott, D. A., & Zhang, F. (2013) · Nature Protocols · doi:10.1038/nprot.2013.143 · Cited by 11,133
Alginate: Properties and biomedical applications
Lee, K. Y., & Mooney, D. J. (2011) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2011.06.003 · Cited by 8,477
Self-citationMolecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin
Aziz, J., Shezali, H., Radzi, Z., Yahya, N. A., Abu Kassim, N. H., Czernuszka, J., & Rahman, M. T. (2016) · Skin Pharmacology and Physiology · doi:10.1159/000447017 · Cited by 7,323
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204
Cerebral organoids model human brain development and microcephaly
Lancaster, M. A., Renner, M., Martin, C.-A., Wenzel, D., Bicknell, L. S., Hurles, M. E., Homfray, T., Penninger, J. M., Jackson, A. P., & Knoblich, J. A. (2013) · Nature · doi:10.1038/nature12517 · Cited by 5,372
Rheinwatd, J. G., & Green, H. (1975) · Cell · doi:10.1016/s0092-8674(75)80001-8 · Cited by 4,581
Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling
Levental, K. R., Yu, H., Kass, L., Lakins, J. N., Egeblad, M., Erler, J. T., Fong, S. F. T., Csiszar, K., Giaccia, A., Weninger, W., et al. (2009) · Cell · doi:10.1016/j.cell.2009.10.027 · Cited by 4,101
Visualization and analysis of gene expression in tissue sections by spatial transcriptomics
Ståhl, P. L., Salmén, F., Vickovic, S., Lundmark, A., Navarro, J. F., Magnusson, J., Giacomello, S., Asp, M., Westholm, J. O., Huss, M., et al. (2016) · Science · doi:10.1126/science.aaf2403 · Cited by 3,834
Sato, T., Stange, D. E., Ferrante, M., Vries, R. G. J., van Es, J. H., van den Brink, S., van Houdt, W. J., Pronk, A., van Gorp, J., Siersema, P. D., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.050 · Cited by 3,753
Stratton, M. R., Campbell, P. J., & Futreal, P. A. (2009) · Nature · doi:10.1038/nature07943 · Cited by 3,625
Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling
Chambers, S. M., Fasano, C. A., Papapetrou, E. P., Tomishima, M., Sadelain, M., & Studer, L. (2009) · Nature Biotechnology · doi:10.1038/nbt.1529 · Cited by 3,620
Organoid Models and Applications in Biomedical Research
Xinaris, C., Brizi, V., & Remuzzi, G. (2015) · The Nephron journals/Nephron journals · doi:10.1159/000433566 · Cited by 3,519
Organogenesis in a dish: Modeling development and disease using organoid technologies
Lancaster, M. A., & Knoblich, J. A. (2014) · Science · doi:10.1126/science.1247125 · Cited by 2,931
Perfusion-decellularized matrix: using nature's platform to engineer a bioartificial heart
Ott, H. C., Matthiesen, T. S., Goh, S.-K., Black, L. D., Kren, S. M., Netoff, T. I., & Taylor, D. A. (2008) · Nature Medicine · doi:10.1038/nm1684 · Cited by 2,650
Hydrogels with tunable stress relaxation regulate stem cell fate and activity
Chaudhuri, O., Gu, L., Klumpers, D., Darnell, M., Bencherif, S. A., Weaver, J. C., Huebsch, N., Lee, H.-P., Lippens, E., Duda, G. N., et al. (2016) · Nature Materials · doi:10.1038/nmat4489 · Cited by 2,443
Prospective Derivation of a Living Organoid Biobank of Colorectal Cancer Patients
van de Wetering, M., Francies, H. E., Francis, J. M., Bounova, G., Iorio, F., Pronk, A., van Houdt, W., van Gorp, J., Taylor-Weiner, A., Kester, L., et al. (2015) · Cell · doi:10.1016/j.cell.2015.03.053 · Cited by 2,408
Capturing complex 3D tissue physiology in vitro
Griffith, L. G., & Swartz, M. A. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1858 · Cited by 2,347
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
Organoid models of human and mouse ductal pancreatic cancer
Boj, S. F., Hwang, C.-I., Baker, L. A., Chio, I. I. C., Engle, D. D., Corbo, V., Jager, M., Ponz-Sarvise, M., Tiriac, H., Spector, M. S., et al. (2015) · Cell · doi:10.1016/j.cell.2014.12.021 · Cited by 2,150
Self-organizing optic-cup morphogenesis in three-dimensional culture
Eiraku, M., Takata, N., Ishibashi, H., Kawada, M., Sakakura, E., Okuda, S., Sekiguchi, K., Adachi, T., & Sasai, Y. (2011) · Nature · doi:10.1038/nature09941 · Cited by 2,001
A living biobank of breast cancer organoids captures disease heterogeneity
Sachs, N., de Ligt, J., Kopper, O., Gogola, E., Bounova, G., Weeber, F., Balgobind, A. V., Wind, K., Gracanin, A., Begthel, H., et al. (2018) · Cell · doi:10.1016/j.cell.2017.11.010 · Cited by 1,973
Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro
Spence, J. R., Mayhew, C. N., Rankin, S. A., Kuhar, M. F., Vallance, J. E., Tolle, K. A., Hoskins, E. E., Kalinichenko, V. V., Wells, S. I., Zorn, A. M., et al. (2010) · Nature · doi:10.1038/nature09691 · Cited by 1,911
Generation of cerebral organoids from human pluripotent stem cells
Lancaster, M. A., & Knoblich, J. A. (2014) · Nature Protocols · doi:10.1038/nprot.2014.158 · Cited by 1,823
Drost, J., & Clevers, H. (2018) · Nature Reviews Cancer · doi:10.1038/s41568-018-0007-6 · Cited by 1,790
Murry, C. E., & Keller, G. M. (2008) · Cell · doi:10.1016/j.cell.2008.02.008 · Cited by 1,760
Polymeric system for dual growth factor delivery
Richardson, T. P., Peters, M. C., Ennett, A. B., & Mooney, D. J. (2001) · Nature Biotechnology · doi:10.1038/nbt1101-1029 · Cited by 1,753
Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver
Huch, M., Gehart, H., van Boxtel, R., Hamer, K., Blokzijl, F., Verstegen, M. M. A., Ellis, E., van Wenum, M., Fuchs, S. A., de Ligt, J., et al. (2015) · Cell · doi:10.1016/j.cell.2014.11.050 · Cited by 1,619
Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture
Paşca, A. M., Sloan, S. A., Clarke, L. E., Tian, Y., Makinson, C. D., Huber, N., Kim, C. H., Park, J.-Y., O'Rourke, N. A., Nguyen, K. D., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3415 · Cited by 1,609
Organoid Cultures Derived from Patients with Advanced Prostate Cancer
Gao, D., Vela, I., Sboner, A., Iaquinta, P. J., Karthaus, W. R., Gopalan, A., Dowling, C., Wanjala, J. N., Undvall, E. A., Arora, V. K., et al. (2014) · Cell · doi:10.1016/j.cell.2014.08.016 · Cited by 1,559
In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration
Huch, M., Dorrell, C., Boj, S. F., van Es, J. H., Li, V. S. W., van de Wetering, M., Sato, T., Hamer, K., Sasaki, N., Finegold, M. J., et al. (2013) · Nature · doi:10.1038/nature11826 · Cited by 1,555
Lgr5+ve Stem Cells Drive Self-Renewal in the Stomach and Build Long-Lived Gastric Units In Vitro
Barker, N., Huch, M., Kujala, P., van de Wetering, M., Snippert, H. J., van Es, J. H., Sato, T., Stange, D. E., Begthel, H., van den Born, M., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2009.11.013 · Cited by 1,547
Matrigel: A complex protein mixture required for optimal growth of cell culture
Hughes, C. S., Postovit, L. M., & Lajoie, G. A. (2010) · PROTEOMICS · doi:10.1002/pmic.200900758 · Cited by 1,534
Eiraku, M., Watanabe, K., Matsuo-Takasaki, M., Kawada, M., Yonemura, S., Matsumura, M., Wataya, T., Nishiyama, A., Muguruma, K., & Sasai, Y. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.09.002 · Cited by 1,522
Human primary liver cancer–derived organoid cultures for disease modeling and drug screening
Broutier, L., Mastrogiovanni, G., Verstegen, M. M., Francies, H. E., Gavarró, L. M., Bradshaw, C. R., Allen, G. E., Arnes-Benito, R., Sidorova, O., Gaspersz, M. P., et al. (2017) · Nature Medicine · doi:10.1038/nm.4438 · Cited by 1,471
Self-formation of optic cups and storable stratified neural retina from human ESCs
Nakano, T., Ando, S., Takata, N., Kawada, M., Muguruma, K., Sekiguchi, K., Saito, K., Yonemura, S., Eiraku, M., & Sasai, Y. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.05.009 · Cited by 1,447
Designer matrices for intestinal stem cell and organoid culture
Gjorevski, N., Sachs, N., Manfrin, A., Giger, S., Bragina, M. E., Ordóñez-Morán, P., Clevers, H., & Lutolf, M. P. (2016) · Nature · doi:10.1038/nature20168 · Cited by 1,426
Schwank, G., Koo, B.-K., Sasselli, V., Dekkers, J. F., Heo, I., Demircan, T., Sasaki, N., Boymans, S., Cuppen, E., van der Ent, C. K., et al. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.11.002 · Cited by 1,424
Uygun, B. E., Soto-Gutierrez, A., Yagi, H., Izamis, M.-L., Guzzardi, M. A., Shulman, C., Milwid, J., Kobayashi, N., Tilles, A., Berthiaume, F., et al. (2010) · Nature Medicine · doi:10.1038/nm.2170 · Cited by 1,370
Cell diversity and network dynamics in photosensitive human brain organoids
Quadrato, G., Nguyen, T., Macosko, E. Z., Sherwood, J. L., Min Yang, S., Berger, D. R., Maria, N., Scholvin, J., Goldman, M., Kinney, J. P., et al. (2017) · Nature · doi:10.1038/nature22047 · Cited by 1,321
Hydrogel microparticles for biomedical applications
Daly, A. C., Riley, L., Segura, T., & Burdick, J. A. (2019) · Nature Reviews Materials · doi:10.1038/s41578-019-0148-6 · Cited by 1,285
Kleinman, H. K., McGarvey, M. L., Liotta, L. A., Robey, P. G., Tryggvason, K., & Martin, G. R. (1982) · Biochemistry · doi:10.1021/bi00267a025 · Cited by 1,231
A three-dimensional human neural cell culture model of Alzheimer’s disease
Choi, S. H., Kim, Y. H., Hebisch, M., Sliwinski, C., Lee, S., D’Avanzo, C., Chen, H., Hooli, B., Asselin, C., Muffat, J., et al. (2014) · Nature · doi:10.1038/nature13800 · Cited by 1,195
Hofer, M., & Lutolf, M. P. (2021) · Nature Reviews Materials · doi:10.1038/s41578-021-00279-y · Cited by 1,184
Progress and potential in organoid research
Rossi, G., Manfrin, A., & Lutolf, M. P. (2018) · Nature Reviews Genetics · doi:10.1038/s41576-018-0051-9 · Cited by 1,182
Mechanical memory and dosing influence stem cell fate
Yang, C., Tibbitt, M. W., Basta, L. P., & Anseth, K. S. (2014) · Nature Materials · doi:10.1038/nmat3889 · Cited by 1,167
FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders
Mariani, J., Coppola, G., Zhang, P., Abyzov, A., Provini, L., Tomasini, L., Amenduni, M., Szekely, A., Palejev, D., Wilson, M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.06.034 · Cited by 1,149
Modeling colorectal cancer using CRISPR-Cas9–mediated engineering of human intestinal organoids
Matano, M., Date, S., Shimokawa, M., Takano, A., Fujii, M., Ohta, Y., Watanabe, T., Kanai, T., & Sato, T. (2015) · Nature Medicine · doi:10.1038/nm.3802 · Cited by 1,135
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
Camp, J. G., Badsha, F., Florio, M., Kanton, S., Gerber, T., Wilsch-Bräuninger, M., Lewitus, E., Sykes, A., Hevers, W., Lancaster, M., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520760112 · Cited by 1,130
Lin, Y.-T., Seo, J., Gao, F., Feldman, H. M., Wen, H.-L., Penney, J., Cam, H. P., Gjoneska, E., Raja, W. K., Cheng, J., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.008 · Cited by 1,125
Individual brain organoids reproducibly form cell diversity of the human cerebral cortex
Velasco, S., Kedaigle, A. J., Simmons, S. K., Nash, A., Rocha, M., Quadrato, G., Paulsen, B., Nguyen, L., Adiconis, X., Regev, A., et al. (2019) · Nature · doi:10.1038/s41586-019-1289-x · Cited by 1,094
Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer
Tiriac, H., Belleau, P., Engle, D. D., Plenker, D., Deschênes, A., Somerville, T. D. D., Froeling, F. E. M., Burkhart, R. A., Denroche, R. E., Jang, G.-H., et al. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-18-0349 · Cited by 1,092
Kadoshima, T., Sakaguchi, H., Nakano, T., Soen, M., Ando, S., Eiraku, M., & Sasai, Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315710110 · Cited by 999
Modelling human development and disease in pluripotent stem-cell-derived gastric organoids
McCracken, K. W., Catá, E. M., Crawford, C. M., Sinagoga, K. L., Schumacher, M., Rockich, B. E., Tsai, Y.-H., Mayhew, C. N., Spence, J. R., Zavros, Y., et al. (2014) · Nature · doi:10.1038/nature13863 · Cited by 980
Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs
Zhong, X., Gutierrez, C., Xue, T., Hampton, C., Vergara, M. N., Cao, L.-H., Peters, A., Park, T. S., Zambidis, E. T., Meyer, J. S., et al. (2014) · Nature Communications · doi:10.1038/ncomms5047 · Cited by 970
Tissue-specific mutation accumulation in human adult stem cells during life
Blokzijl, F., de Ligt, J., Jager, M., Sasselli, V., Roerink, S., Sasaki, N., Huch, M., Boymans, S., Kuijk, E., Prins, P., et al. (2016) · Nature · doi:10.1038/nature19768 · Cited by 935
Cancer modeling meets human organoid technology
Tuveson, D., & Clevers, H. (2019) · Science · doi:10.1126/science.aaw6985 · Cited by 935
Deterministically patterned biomimetic human iPSC-derived hepatic model via rapid 3D bioprinting
Ma, X., Qu, X., Zhu, W. Z., Li, Y.-S. J., Yuan, S., Zhang, H., Liu, J., Wang, P., Lai, C. S. E., Zanella, F., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1524510113 · Cited by 881
Taguchi, A., Kaku, Y., Ohmori, T., Sharmin, S., Ogawa, M., Sasaki, H., & Nishinakamura, R. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.11.010 · Cited by 871
In vitro generation of human pluripotent stem cell derived lung organoids
Dye, B. R., Hill, D. R., Ferguson, M. A. H., Tsai, Y.-H., Nagy, M. S., Dyal, R., Wells, J. M., Mayhew, C. N., Nattiv, R., Klein, O. D., et al. (2015) · eLife · doi:10.7554/elife.05098 · Cited by 846
Long-Term Expansion of Functional Mouse and Human Hepatocytes as 3D Organoids
Hu, H., Gehart, H., Artegiani, B., LÖpez-Iglesias, C., Dekkers, F., Basak, O., van Es, J., Chuva de Sousa Lopes, S. M., Begthel, H., Korving, J., et al. (2018) · Cell · doi:10.1016/j.cell.2018.11.013 · Cited by 837
In Vitro Expansion of Human Gastric Epithelial Stem Cells and Their Responses to Bacterial Infection
Bartfeld, S., Bayram, T., van de Wetering, M., Huch, M., Begthel, H., Kujala, P., Vries, R., Peters, P. J., & Clevers, H. (2015) · Gastroenterology · doi:10.1053/j.gastro.2014.09.042 · Cited by 820
Making a commitment: cell lineage allocation and axis patterning in the early mouse embryo
Arnold, S. J., & Robertson, E. J. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2618 · Cited by 816
Vertebrate Endoderm Development and Organ Formation
Zorn, A. M., & Wells, J. M. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113344 · Cited by 812
Freedman, B., Brooks, C. R., Lam, A. Q., Fu, H., Morizane, R., Agrawal, V., Saad, A. F., Li, M. K., Hughes, M. R., Werff, R. V., et al. (2015) · Nature Communications · doi:10.1038/ncomms9715 · Cited by 803
Enaud, R., Prével, R., Ciarlo, E., Beaufils, F., Wieërs, G., Guery, B. P., & Delhaès, L. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00009 · Cited by 786
Directed differentiation of telencephalic precursors from embryonic stem cells
Watanabe, K., Kamiya, D., Nishiyama, A., Katayama, T., Nozaki, S., Kawasaki, H., Watanabe, Y., Mizuseki, K., & Sasai, Y. (2005) · Nature Neuroscience · doi:10.1038/nn1402 · Cited by 784
Guided self-organization and cortical plate formation in human brain organoids
Lancaster, M. A., Corsini, N. S., Wolfinger, S., Gustafson, E. H., Phillips, A. W., Burkard, T. R., Otani, T., Livesey, F. J., & Knoblich, J. A. (2017) · Nature Biotechnology · doi:10.1038/nbt.3906 · Cited by 783
Acellular vascular tissues: natural biomaterials for tissue repair and tissue engineering
Schmidt, C. E., & Baier, J. M. (2000) · Biomaterials · doi:10.1016/s0142-9612(00)00148-4 · Cited by 762
Huang, L., Holtzinger, A., Jagan, I., BeGora, M. D., Lohse, I., Ngai, N., Nostro, M. C., Wang, R., Muthuswamy, L. B., Crawford, H. C., et al. (2015) · Nature Medicine · doi:10.1038/nm.3973 · Cited by 745
Identification of Multipotent Luminal Progenitor Cells in Human Prostate Organoid Cultures
Karthaus, W. R., Iaquinta, P. J., Drost, J., Gracanin, A., van Boxtel, R., Wongvipat, J., Dowling, C., Gao, D., Begthel, H., Sachs, N., et al. (2014) · Cell · doi:10.1016/j.cell.2014.08.017 · Cited by 739
Unlimited in vitro expansion of adult bi‐potent pancreas progenitors through the Lgr5/R‐spondin axis
Huch, M., Bonfanti, P., Boj, S. F., Sato, T., Loomans, C. J. M., van de Wetering, M., Sojoodi, M., Li, V. S. W., Schuijers, J., Gracanin, A., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.204 · Cited by 726
Brain organoids: advances, applications and challenges
Qian, X., Song, H., & Ming, G.-L. (2019) · Development · doi:10.1242/dev.166074 · Cited by 724
Barcellos‐Hoff, M. H., Aggeler, J., Ram, T. G., & Bissell, M. J. (1989) · Development · doi:10.1242/dev.105.2.223 · Cited by 714
Establishment of patient-derived cancer organoids for drug-screening applications
Driehuis, E., Kretzschmar, K., & Clevers, H. C. (2020) · Nature Protocols · doi:10.1038/s41596-020-0379-4 · Cited by 702
Cerebral organoids at the air-liquid interface generate diverse nerve tracts with functional output
Giandomenico, S. L., Mierau, S. B., Gibbons, G. M., Wenger, L. M. D., Masullo, L., Sit, T., Sutcliffe, M., Boulanger, J., Tripodi, M., Derivery, E., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0350-2 · Cited by 651
Microglia innately develop within cerebral organoids
Ormel, P. R., de Sá, R. V., van Bodegraven, E. J., Karst, H., Harschnitz, O., Sneeboer, M. A. M., Johansen, L. E., van Dijk, R. E., Scheefhals, N., van Berlekom, A. B., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06684-2 · Cited by 642
Cell stress in cortical organoids impairs molecular subtype specification
Bhaduri, A., Andrews, M. G., Mancia Leon, W., Jung, D., Shin, D., Allen, D., Jung, D., Schmunk, G., Haeussler, M., Salma, J., et al. (2020) · Nature · doi:10.1038/s41586-020-1962-0 · Cited by 624
Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform
Skardal, A., Murphy, S. V., Devarasetty, M., Mead, I., Kang, H.-W., Seol, Y.-J., Shrike Zhang, Y., Shin, S.-R., Zhao, L., Aleman, J., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-08879-x · Cited by 623
Self-citationMl, L., Aggeler, J., Farson, D. A., Hatier, C., Hassell, J. R., & Bissell, M. J. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.1.136 · Cited by 620
Modeling mouse and human development using organoid cultures
Huch, M., & Koo, B. (2015) · Development · doi:10.1242/dev.118570 · Cited by 578
Synthetic hydrogels for human intestinal organoid generation and colonic wound repair
Cruz-Acuña, R., Quirós, M., Farkas, A. E., Dedhia, P. H., Huang, S., Siuda, D., García-Hernández, V., Miller, A. J., Spence, J. R., Nusrat, A., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3632 · Cited by 558
High-resolution 3D imaging of fixed and cleared organoids
Dekkers, J. F., Alieva, M., Wellens, L. M., Ariese, H. C., Jamieson, P. R., Vonk, A. M., Amatngalim, G. D., Hu, H., Oost, K. C., Snippert, H. J. G., et al. (2019) · Nature Protocols · doi:10.1038/s41596-019-0160-8 · Cited by 558
A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns
Notta, F., Chan-Seng-Yue, M., Lemire, M., Li, Y., Wilson, G. W., Connor, A. A., Denroche, R. E., Liang, S.-B., Brown, A. M. K., Kim, J. C., et al. (2016) · Nature · doi:10.1038/nature19823 · Cited by 528
Generation of human brain region–specific organoids using a miniaturized spinning bioreactor
Qian, X., Jacob, F., Song, M. M., Nguyen, H. N., Song, H., & Ming, G. (2018) · Nature Protocols · doi:10.1038/nprot.2017.152 · Cited by 528
Reliability of human cortical organoid generation
Yoon, S.-J., Elahi, L. S., Pașca, A. M., Marton, R. M., Gordon, A., Revah, O., Miura, Y., Walczak, E. M., Holdgate, G. M., Fan, H. C., et al. (2019) · Nature Methods · doi:10.1038/s41592-018-0255-0 · Cited by 507
Badylak, S. F., Tullius, R. S., Kokini, K., Shelbourne, K. D., Klootwyk, T. E., Voytik, S. L., Kraine, M. R., & Simmons, C. (1995) · Journal of Biomedical Materials Research · doi:10.1002/jbm.820290809 · Cited by 501
Tumor Organoids as a Pre-clinical Cancer Model for Drug Discovery
Weeber, F., Ooft, S., Dijkstra, K. K., & Voest, E. E. (2017) · Cell chemical biology · doi:10.1016/j.chembiol.2017.06.012 · Cited by 501
Giobbe, G. G., Crowley, C., Luni, C., Campinoti, S., Khedr, M., Kretzschmar, K., De Santis, M. M., Zambaiti, E., Michielin, F., Meran, L., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13605-4 · Cited by 500
Generation and assembly of human brain region-specific three-dimensional cultures
Sloan, S. A., Andersen, J., Pașca, A. M., Birey, F., & Pașca, S. P. (2018) · Nature Protocols · doi:10.1038/s41596-018-0032-7 · Cited by 490
Hair-bearing human skin generated entirely from pluripotent stem cells
Lee, J., Rabbani, C. C., Gao, H., Steinhart, M. R., Woodruff, B. M., Pflum, Z. E., Kim, A., Heller, S., Liu, Y., Shipchandler, T. Z., et al. (2020) · Nature · doi:10.1038/s41586-020-2352-3 · Cited by 487
Cytosystems dynamics in self-organization of tissue architecture
Sasai, Y. (2013) · Nature · doi:10.1038/nature11859 · Cited by 484
Fabrication of microfluidic hydrogels using molded gelatin as a sacrificial element
Golden, A. P., & Tien, J. (2007) · Lab on a Chip · doi:10.1039/b618409j · Cited by 479
Human CNS barrier-forming organoids with cerebrospinal fluid production
Pellegrini, L., Bonfio, C., Chadwick, J., Begum, F., Skehel, M. J., & Lancaster, M. A. (2020) · Science · doi:10.1126/science.aaz5626 · Cited by 471
Recapitulating macro-scale tissue self-organization through organoid bioprinting
Brassard, J. A., Nikolaev, M., Hübscher, T., Hofer, M., & Lutolf, M. P. (2021) · Nature Materials · doi:10.1038/s41563-020-00803-5 · Cited by 469
Induced pluripotent stem cells: the new patient?
Bellin, M., Marchetto, M. C., Gage, F. H., & Mummery, C. L. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3448 · Cited by 454
Engineered materials for organoid systems
Kratochvil, M. J., Seymour, A. J., Li, T. L., Pașca, S. P., Kuo, C. J., & Heilshorn, S. C. (2019) · Nature Reviews Materials · doi:10.1038/s41578-019-0129-9 · Cited by 430
Human brain organoids on a chip reveal the physics of folding
Karzbrun, E., Kshirsagar, A., Cohen, S., Hanna, J. H., & Reiner, O. (2018) · Nature Physics · doi:10.1038/s41567-018-0046-7 · Cited by 421
Takebe, T., & Wells, J. M. (2019) · Science · doi:10.1126/science.aaw7567 · Cited by 417
The dissociation and aggregation of cells from organ rudiments of the early chick embryo.
(1952) · Europe PMC (PubMed Central) · Cited by 414
Vascularized human cortical organoids (vOrganoids) model cortical development in vivo
Shi, Y., Sun, L., Liu, J., Zhong, S., Wang, M., Li, R., Li, P., Guo, L., Fang, A., Chen, R., et al. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000705 · Cited by 412
Laminin mediates tissue-specific gene expression in mammary epithelia.
Streuli, C. H., Schmidhauser, C., Bailey, N., Yurchenco, P. D., Skubitz, A. P. N., Roskelley, C. D., & Bissell, M. J. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.129.3.591 · Cited by 404
Maintenance of neural progenitor cell stemness in 3D hydrogels requires matrix remodelling
Madl, C. M., LeSavage, B. L., Dewi, R. E., Dinh, C. B., Stowers, R. S., Khariton, M., Lampe, K. J., Nguyen, D., Chaudhuri, O., Enejder, A. M. K., et al. (2017) · Nature Materials · doi:10.1038/nmat5020 · Cited by 399
Engineering Stem Cell Self-organization to Build Better Organoids
Brassard, J. A., & Lütolf, M. P. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.05.005 · Cited by 392
Self‐organized developmental patterning and differentiation in cerebral organoids
Renner, M., Lancaster, M. A., Bian, S., Choi, H., Ku, T., Peer, A., Chung, K., & Knoblich, J. A. (2017) · The EMBO Journal · doi:10.15252/embj.201694700 · Cited by 389
Bioinspired neuron-like electronics
Yang, X., Zhou, T., Zwang, T. J., Hong, G., Zhao, Y., Viveros, R. D., Fu, T.-M., Gao, T., & Lieber, C. M. (2019) · Nature Materials · doi:10.1038/s41563-019-0292-9 · Cited by 384
Vascularized organoid engineered by modular assembly enables blood perfusion
McGuigan, A. P., & Sefton, M. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602740103 · Cited by 372
Modeling Parkinson’s disease in midbrain-like organoids
Smits, L. M., Reinhardt, L., Reinhardt, P., Glatza, M., Monzel, A. S., Stanslowsky, N., Rosato‐Siri, M. D., Zanon, A., Antony, P. M. A., Bellmann, J., et al. (2019) · npj Parkinson s Disease · doi:10.1038/s41531-019-0078-4 · Cited by 368
Generation of a vascularized and functional human liver from an iPSC-derived organ bud transplant
Takebe, T., Zhang, R., Koike, H., Kimura, M., Yoshizawa, E., Enomura, M., Koike, N., Sekine, K., & Taniguchi, H. (2014) · Nature Protocols · doi:10.1038/nprot.2014.020 · Cited by 366
Modeling G2019S-LRRK2 Sporadic Parkinson's Disease in 3D Midbrain Organoids
Kim, H., Park, H. J., Choi, H. G., Chang, Y., Park, H., Shin, J., Kim, J., Lengner, C. J., Lee, Y. K., & Kim, J. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.01.020 · Cited by 362
Boundary formation and maintenance in tissue development
Dahmann, C., Oates, A. C., & Brand, M. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2902 · Cited by 352
Self-Organizing 3D Human Trunk Neuromuscular Organoids
Martins, J.-M. F., Fischer, C., Urzi, A., Vidal, R. O., Kunz, S., Ruffault, P.-L., Kabuss, L., Hube, I., Gazzerro, E., Birchmeier, C., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2019.12.007 · Cited by 339
Generation of kidney organoids from human pluripotent stem cells
Takasato, M., Er, P. X., Chiu, H. S., & Little, M. H. (2016) · Nature Protocols · doi:10.1038/nprot.2016.098 · Cited by 334
Specification of positional identity in forebrain organoids
Cederquist, G., Asciolla, J. J., Tchieu, J. H., Walsh, R. M., Cornacchia, D., Resh, M. D., & Studer, L. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0085-3 · Cited by 334
McCauley, H. A., & Wells, J. M. (2017) · Development · doi:10.1242/dev.140731 · Cited by 322
Artegiani, B., Hendriks, D. F. G., Beumer, J., Kok, R. N. U., Zheng, X., Joore, I. P., Lopes, S. M. C. D. S., van Zon, J. S., Tans, S. J., & Clevers, H. C. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-0472-5 · Cited by 313
Building Models of Brain Disorders with Three-Dimensional Organoids
Amin, N. D., & Paşca, S. P. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.007 · Cited by 312
YAP/TAZ link cell mechanics to Notch signalling to control epidermal stem cell fate
Totaro, A., Castellan, M., Battilana, G., Zanconato, F., Azzolin, L., Giulitti, S., Cordenonsi, M., & Piccolo, S. (2017) · Nature Communications · doi:10.1038/ncomms15206 · Cited by 299
Process development of an acellular dermal matrix (ADM) for biomedical applications
Chen, R.-N., Ho, H., Tsai, Y.-T., & Sheu, M. (2003) · Biomaterials · doi:10.1016/j.biomaterials.2003.09.070 · Cited by 298
Engineering Organoid Vascularization
Grebenyuk, S., & Ranga, A. (2019) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2019.00039 · Cited by 295
Sridhar, A., Hoshino, A., Finkbeiner, C., Chitsazan, A., Dai, L., Haugan, A. K., Eschenbacher, K. M., Jackson, D. L., Trapnell, C., Bermingham‐McDonogh, O., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.007 · Cited by 291
Growth of Epithelial Organoids in a Defined Hydrogel
Broguiere, N., Isenmann, L., Hirt, C., Ringel, T., Placzek, S., Cavalli, E., Ringnalda, F., Villiger, L., Züllig, R., Lehmann, R., et al. (2018) · Advanced Materials · doi:10.1002/adma.201801621 · Cited by 282
Dekkers, J. F., van Vliet, E. J., Sachs, N., Rosenbluth, J. M., Kopper, O., Rebel, H. G., Wehrens, E. J., Piani, C., Visvader, J. E., Veríssimo, C. S., et al. (2021) · Nature Protocols · doi:10.1038/s41596-020-00474-1 · Cited by 282
Perfusion decellularization of whole organs
Guyette, J. P., Gilpin, S. E., Charest, J. M., Tapias, L. F., Ren, X., & Ott, H. C. (2014) · Nature Protocols · doi:10.1038/nprot.2014.097 · Cited by 275
Biomaterials and engineered microenvironments to control YAP/TAZ-dependent cell behaviour
Brusatin, G., Panciera, T., Gandin, A., Citron, A., & Piccolo, S. (2018) · Nature Materials · doi:10.1038/s41563-018-0180-8 · Cited by 274
Tissue engineering by decellularization and 3D bioprinting
Garreta, E., Oria, R., Tarantino, C., Pla‐Roca, M., Prado, P., Fernández‐Avilés, F., Campistol, J. M., Samitier, J., & Montserrat, N. (2017) · Materials Today · doi:10.1016/j.mattod.2016.12.005 · Cited by 273
Defined three-dimensional microenvironments boost induction of pluripotency
Caiazzo, M., Okawa, Y., Ranga, A., Piersigilli, A., Tabata, Y., & Lutolf, M. P. (2016) · Nature Materials · doi:10.1038/nmat4536 · Cited by 271
A 3D human neural cell culture system for modeling Alzheimer's disease
Kim, Y. H., Choi, S. H., D'Avanzo, C., Hebisch, M., Sliwinski, C., Bylykbashi, E., Washicosky, K. J., Klee, J. B., Brüstle, O., Tanzi, R. E., et al. (2015) · Nature Protocols · doi:10.1038/nprot.2015.065 · Cited by 269
Evaluation of variability in human kidney organoids
Phipson, B., Er, P. X., Combes, A. N., Forbes, T. A., Howden, S. E., Zappia, L., Yen, H.-J., Lawlor, K. T., Hale, L. J., Sun, J. Q. J., et al. (2018) · Nature Methods · doi:10.1038/s41592-018-0253-2 · Cited by 264
Generation of nephron progenitor cells and kidney organoids from human pluripotent stem cells
Morizane, R., & Bonventre, J. V. (2016) · Nature Protocols · doi:10.1038/nprot.2016.170 · Cited by 243
Material Cues as Potent Regulators of Epigenetics and Stem Cell Function
Crowder, S. W., Leonardo, V., Whittaker, T. E., Papathanasiou, P., & Stevens, M. M. (2016) · Cell stem cell · doi:10.1016/j.stem.2015.12.012 · Cited by 234
Stem cell-derived organoids and their application for medical research and patient treatment
Bartfeld, S., & Clevers, H. C. (2017) · Journal of Molecular Medicine · doi:10.1007/s00109-017-1531-7 · Cited by 226
Nonadhesive Alginate Hydrogels Support Growth of Pluripotent Stem Cell-Derived Intestinal Organoids
Capeling, M. M., Czerwinski, M., Huang, S., Tsai, Y.-H., Wu, A., Nagy, M. S., Juliar, B., Sundaram, N., Song, Y., Han, W. M., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.12.001 · Cited by 226
Li, Q., Nan, K., Le Floch, P., Lin, Z., Sheng, H., Blum, T. S., & Liu, J. (2019) · Nano Letters · doi:10.1021/acs.nanolett.9b02512 · Cited by 224
Decellularized human valve allografts
Elkins, R. C., Dawson, P. E., Goldstein, S., Walsh, S. P., & Black, K. S. (2001) · The Annals of Thoracic Surgery · doi:10.1016/s0003-4975(01)02503-6 · Cited by 223
CRISPR-Based Adenine Editors Correct Nonsense Mutations in a Cystic Fibrosis Organoid Biobank
Geurts, M. H., de Poel, E., Amatngalim, G. D., Oka, R., Meijers, F. M., Kruisselbrink, E., van Mourik, P., Berkers, G., de Winter-de Groot, K. M., Michel, S., et al. (2020) · Cell Stem Cell · doi:10.1016/j.stem.2020.01.019 · Cited by 222
Michels, B. E., Mosa, M. H., Streibl, B. I., Zhan, T., Menche, C., Abou-El-Ardat, K., Darvishi, T., Członka, E., Wagner, S., Winter, J., et al. (2020) · Cell Stem Cell · doi:10.1016/j.stem.2020.04.003 · Cited by 222
Neural tube morphogenesis in synthetic 3D microenvironments
Ranga, A., Girgin, M., Meinhardt, A., Eberle, D., Caiazzo, M., Tanaka, E. M., & Lutolf, M. P. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1603529113 · Cited by 221
Vascularization and Engraftment of Transplanted Human Cerebral Organoids in Mouse Cortex
Daviaud, N., Friedel, R. H., & Zou, H. (2018) · eNeuro · doi:10.1523/eneuro.0219-18.2018 · Cited by 219
Probing the Tumor Suppressor Function of BAP1 in CRISPR-Engineered Human Liver Organoids
Artegiani, B., van Voorthuijsen, L., Lindeboom, R. G. H., Seinstra, D., Heo, I., Tapia, P., López-Iglesias, C., Postrach, D., Dayton, T., Oka, R., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.04.017 · Cited by 218
Neuroimmune circuits in inter-organ communication
Huh, J. R., & Veiga‐Fernandes, H. (2019) · Nature reviews. Immunology · doi:10.1038/s41577-019-0247-z · Cited by 216
Lee, J. W., Komar, C. A., Bengsch, F., Graham, K. L., & Beatty, G. L. (2016) · Current Protocols in Pharmacology · doi:10.1002/cpph.2 · Cited by 212
Subramanian, A., Sidhom, E.-H., Emani, M., Vernon, K., Sahakian, N., Zhou, Y., Kost-Alimova, M., Slyper, M., Waldman, J., Dionne, D., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13382-0 · Cited by 211
YAP-independent mechanotransduction drives breast cancer progression
Lee, J. Y., Chang, J. K., Dominguez, A. A., Lee, H.-P., Nam, S., Chang, J., Varma, S., Qi, L. S., West, R. B., & Chaudhuri, O. (2019) · Nature Communications · doi:10.1038/s41467-019-09755-0 · Cited by 209
Genetically targeted chemical assembly of functional materials in living cells, tissues, and animals
Jia Liu, B., Kim, Y. S., Richardson, C. E., Tom, A., Ramakrishnan, C., Birey, F., Katsumata, T., Chen, S., Wang, C., Wang, X., et al. (2020) · Science · doi:10.1126/science.aay4866 · Cited by 206
Weiss, P. A., & Taylor, A. C. (1960) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.46.9.1177 · Cited by 201
Injectable and Conductive Granular Hydrogels for 3D Printing and Electroactive Tissue Support
Shin, M., Song, K. H., Burrell, J. C., Cullen, D. K., & Burdick, J. A. (2019) · Advanced Science · doi:10.1002/advs.201901229 · Cited by 196
In Situ Patterning of Microfluidic Networks in 3D Cell‐Laden Hydrogels
Brandenberg, N., & Lütolf, M. P. (2016) · Advanced Materials · doi:10.1002/adma.201601099 · Cited by 195
Swimming muscles power suction feeding in largemouth bass
Camp, A. L., Roberts, T. J., & Brainerd, E. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508055112 · Cited by 193
Hirschsprung's disease in Japan: analysis of 3852 patients based on a nationwide survey in 30 years
Suita, S., Taguchi, T., Ieiri, S., & Nakatsuji, T. (2005) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2004.09.052 · Cited by 185
Microfluidic-enabled bottom-up hydrogels from annealable naturally-derived protein microbeads
Sheikhi, A., de Rutte, J. M., Haghniaz, R., Akouissi, O., Sohrabi, A., Carlo, D. D., & Khademhosseini, A. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.10.040 · Cited by 181
Emerging tumor spheroids technologies for 3D in vitro cancer modeling
Rodrigues, T., Kundu, B., Silva-Correia, J., Kundu, S. C., Oliveira, J. M., Reis, R. L., & Correlo, V. M. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2017.10.018 · Cited by 178
Hernandez‐Gordillo, V., Kassis, T., Lampejo, A. O., Choi, G., Gamboa, M. E., Gnecco, J. S., Brown, A., Breault, D. T., Carrier, R. L., & Griffith, L. G. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2020.120125 · Cited by 177
Hydrogel-based colorectal cancer organoid co-culture models
Luo, X., Fong, E. L. S., Zhu, C., Lin, Q. X. X., Xiong, M., Li, A., Li, T., Benoukraf, T., Yu, H., & Liu, S. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.12.037 · Cited by 177
Inspiration from heart development: Biomimetic development of functional human cardiac organoids
Richards, D. J., Coyle, R. C., Tan, Y., Jia, J., Wong, K., Toomer, K., Menick, D. R., & Mei, Y. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.07.021 · Cited by 166
Takezawa, T., Ozaki, K., Nitani, A., Takabayashi, C., & Shimo-Oka, T. (2004) · Cell Transplantation · doi:10.3727/000000004783983882 · Cited by 165
Wilkinson, D. C., Alva-Ornelas, J. A., Sucre, J. M. S., Vijayaraj, P., Durra, A., Richardson, W., Jonas, S. J., Paul, M. K., Karumbayaram, S., Dunn, B., et al. (2017) · Stem Cells Translational Medicine · doi:10.5966/sctm.2016-0192 · Cited by 165
Pashos, E. E., Park, Y., Wang, X., Raghavan, A., Yang, W., Abbey, D., Peters, D., Arbelaez, J., Hernandez, M., Kuperwasser, N., et al. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.03.017 · Cited by 162
Robust, Long-Term Culture of Endoderm-Derived Hepatic Organoids for Disease Modeling
Akbari, S., Sevinç, G. G., Ersoy, N., Başak, O., Kaplan, K. N., Sevinç, K., Ozel, E., Şengün, B., Enüstün, E., Özçimen, B., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.08.007 · Cited by 158
Inhibition of p25/Cdk5 Attenuates Tauopathy in Mouse and iPSC Models of Frontotemporal Dementia
Seo, J., Kritskiy, O., Watson, L. A., Barker, S. J., Dey, D., Raja, W. K., Lin, Y.-T., Ko, T., Cho, S., Penney, J., et al. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.0621-17.2017 · Cited by 156
Gjorevski, N., & Lütolf, M. P. (2017) · Nature Protocols · doi:10.1038/nprot.2017.095 · Cited by 154
Electro‐Assisted Bioprinting of Low‐Concentration GelMA Microdroplets
Xie, M., Gao, Q., Zhao, H., Nie, J., Fu, Z., Wang, H., Chen, L., Shao, L., Fu, J., Chen, Z., et al. (2018) · Small · doi:10.1002/smll.201804216 · Cited by 144
Biomaterials‐Based Approaches to Tumor Spheroid and Organoid Modeling
Thakuri, P. S., Liu, C., Luker, G. D., & Tavana, H. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201700980 · Cited by 142
Lindborg, B. A., Brekke, J. H., Vegoe, A. L., Ulrich, C. B., Haider, K. T., Subramaniam, S., Venhuizen, S. L., Eide, C. R., Orchard, P. J., Chen, W., et al. (2016) · Stem Cells Translational Medicine · doi:10.5966/sctm.2015-0305 · Cited by 141
The origin of the mammalian kidney: implications for recreating the kidney in vitro
Takasato, M., & Little, M. H. (2015) · Development · doi:10.1242/dev.104802 · Cited by 135
Ng, S. S., Saeb-Parsy, K., Blackford, S. J. I., Segal, J. M., Serra, M. P., Horcas-Lopez, M., No, D. Y., Mastoridis, S., Jassem, W., Frank, C. W., et al. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.07.043 · Cited by 133
Use of bioreactors for culturing human retinal organoids improves photoreceptor yields
Ovando-Roche, P., West, E. L., Branch, M. J., Sampson, R. D., Fernando, M., Munro, P., Georgiadis, A., Rizzi, M., Kloc, M., Naeem, A., et al. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-018-0907-0 · Cited by 127
Enemchukwu, N. O., Cruz‐Acuña, R., Bongiorno, T., Johnson, C. T., García, J. R., Sulchek, T., & Garcı́a, A. J. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201506055 · Cited by 125
Microrheological Characterization of Collagen Systems: From Molecular Solutions to Fibrillar Gels
Shayegan, M., & Forde, N. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070590 · Cited by 114
Non-myogenic Contribution to Muscle Development and Homeostasis: The Role of Connective Tissues
Nassari, S., Duprez, D., & Fournier‐Thibault, C. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2017.00022 · Cited by 111
Is this a brain which I see before me? Modeling human neural development with pluripotent stem cells
Suzuki, I. K., & Vanderhaeghen, P. (2015) · Development · doi:10.1242/dev.120568 · Cited by 110
Polymer Hydrogels to Guide Organotypic and Organoid Cultures
Magno, V., Meinhardt, A., & Werner, C. (2020) · Advanced Functional Materials · doi:10.1002/adfm.202000097 · Cited by 110
Schultheiss, D., Gabouev, A. I., Cebotari, S., Tudorache, I., WALLES, T., Schlote, N., Wefer, J., Kaufmann, P. M., Haverich, A., Udo Jonas, A., et al. (2005) · The Journal of Urology · doi:10.1097/01.ju.0000145882.80339.18 · Cited by 105
Chen, Y., Zhou, W., Roh, T. T., Estes, M. K., & Kaplan, D. L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187880 · Cited by 105
Ng, S., Tan, W. J., Pek, M. M. X., Tan, M.-H., & Kurisawa, M. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.119400 · Cited by 105
Bi, H., Ye, K., & Jin, S. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2019.119673 · Cited by 105
Haga, K., Ettayebi, K., Tenge, V. R., Karandikar, U. C., Lewis, M. A., Lin, S., Neill, F. H., Ayyar, B. V., Zeng, X., Larson, G., et al. (2020) · mBio · doi:10.1128/mbio.00251-20 · Cited by 105
Hushka, E. A., Yavitt, F. M., Brown, T. E., Dempsey, P. J., & Anseth, K. S. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.201901214 · Cited by 104
Xia, Y. F., Sancho-Martinez, I., Nivet, E., Esteban, C. R., Campistol, J. M., & Belmonte, J. C. I. (2014) · Nature Protocols · doi:10.1038/nprot.2014.182 · Cited by 99
Mesenchymal Stem Cells Increase Alveolar Differentiation in Lung Progenitor Organoid Cultures
Leeman, K. T., Pessina, P., Lee, J., & Kim, C. F. (2019) · Scientific Reports · doi:10.1038/s41598-019-42819-1 · Cited by 99
DIFFERENTIATION OF MESENCHYMAL LIMB BUD CELLS TO CHONDROCYTES IN ALGINATE BEADS
Shakibaei, M., & SOUZA, P. D. (1997) · Cell Biology International · doi:10.1006/cbir.1996.0119 · Cited by 96
Toward single cell traction microscopy within 3D collagen matrices
Hall, M. S., Long, R., Feng, X., Huang, Y., Hui, C., & Wu, M. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.06.009 · Cited by 95
Cellulose Nanofibril Hydrogel Promotes Hepatic Differentiation of Human Liver Organoids
Krüger, M., Oosterhoff, L. A., van Wolferen, M. E., Schiele, S., Walther, A., Geijsen, N., Laporte, L. D., van der Laan, L. J. W., Kock, L. M., & Spee, B. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.201901658 · Cited by 93
Morphogenesis Guided by 3D Patterning of Growth Factors in Biological Matrices
Broguière, N., Lüchtefeld, I., Trachsel, L., Mazunin, D., Rizzo, R., Bode, J. W., Lütolf, M. P., & Zenobi‐Wong, M. (2020) · Advanced Materials · doi:10.1002/adma.201908299 · Cited by 93
Rowland, C. R., Glass, K. A., Ettyreddy, A. R., Gloss, C. C., Matthews, J. R. L., Huynh, N. P. T., & Guilak, F. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.04.049 · Cited by 92
Standardized GMP-compliant scalable production of human pancreas organoids
Dossena, M., Piras, R., Cherubini, A., Barilani, M., Dugnani, E., Salanitro, F., Moreth, T., Pampaloni, F., Piemonti, L., & Lazzari, L. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-1585-2 · Cited by 87
Gawade, P. M., Shadish, J. A., Badeau, B. A., & DeForest, C. A. (2019) · Advanced Materials · doi:10.1002/adma.201902462 · Cited by 86
Dissecting the stem cell niche with organoid models: an engineering-based approach
Murrow, L. M., Weber, R. J., & Gartner, Z. J. (2017) · Development · doi:10.1242/dev.140905 · Cited by 85
Ke, M., Yuan, X. N., He, A., Yu, P., Chen, W., Shi, Y., Hunter, T. R., Zou, P., & Tian, R. (2021) · Nature Communications · doi:10.1038/s41467-020-20367-x · Cited by 71
Protein-engineered scaffolds for in vitro 3D culture of primary adult intestinal organoids
DiMarco, R. L., Dewi, R. E., Bernal, G., Kuo, C., & Heilshorn, S. C. (2015) · Biomaterials Science · doi:10.1039/c5bm00108k · Cited by 66
Bioprinting Cellularized Constructs Using a Tissue-specific Hydrogel Bioink
Skardal, A., Devarasetty, M., Kang, H.-W., Seol, Y.-J., Forsythe, S. D., Bishop, C., Shupe, T., Soker, S., & Atala, A. (2016) · Journal of Visualized Experiments · doi:10.3791/53606 · Cited by 65
The challenge of developing human 3D organoids into medicines
Vives, J., & Batlle-Morera, L. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-1586-1 · Cited by 65
Organoid Center Strategies for Accelerating Clinical Translation
Takebe, T., Wells, J. M., Helmrath, M. A., & Zorn, A. M. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.05.008 · Cited by 64
Constructing and Deconstructing Cancers using Human Pluripotent Stem Cells and Organoids
Smith, R. C., & Tabar, V. S. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.11.012 · Cited by 62
Hydrogel-based milliwell arrays for standardized and scalable retinal organoid cultures
Decembrini, S., Hoehnel, S., Brandenberg, N., Arsenijévic, Y., & Lütolf, M. P. (2020) · Scientific Reports · doi:10.1038/s41598-020-67012-7 · Cited by 62
Woo, D., Chen, Q., Yang, T.-L., Glineburg, M. R., Hoge, C., Leu, N. A., Johnson, F. B., & Lengner, C. J. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.05.024 · Cited by 61
Automated Design of Pluripotent Stem Cell Self-Organization
Libby, A. R. G., Briers, D., Haghighi, I., Joy, D. A., Conklin, B. R., Belta, C. A., & McDevitt, T. C. (2019) · Cell Systems · doi:10.1016/j.cels.2019.10.008 · Cited by 61
Shin, H.-S., Hong, H. J., Koh, W., & Lim, J. (2018) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b00894 · Cited by 60
Development of Islet Organoids from H9 Human Embryonic Stem Cells in Biomimetic 3D Scaffolds
Wang, W.-W., Jin, S., & Ye, K.-M. (2017) · Stem Cells and Development · doi:10.1089/scd.2016.0115 · Cited by 59
High resolution bioprinting of multi-component hydrogels
Zimmermann, R., Hentschel, C., Schrön, F., Moedder, D., Büttner, T., Atallah, P., Wegener, T., Gehring, T., Howitz, S., Freudenberg, U., et al. (2019) · Biofabrication · doi:10.1088/1758-5090/ab2aa1 · Cited by 56
Research works printed but not linked: 7
- Moscona A., 1952, J. Anat., 86, 287
- Qian X., 2019, Development, 146
- Borenstein J. T., 2004, Architecture and Application of Biomaterials and Biomolecular Materials, 9
- Maile S., 2000, Histol. Histopathol., 15, 403
- Luo X., 2020, Acta Biomater.
- Skardal A., 2016, J. Vis. Exp.
- Lee H. J., 2021, ACS Biomater. Sci. Eng.
Cited by
Sorted by citations
Zhao, Z., Chen, X., Dowbaj, A. M., Sljukic, A., Bratlie, K., Lin, L., Fong, E. L. S., Balachander, G. M., Chen, Z., Soragni, A., et al. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00174-y · Cited by 1,082
Three-Dimensional Cell Cultures: The Bridge between In Vitro and In Vivo Models
Urzì, O., Gasparro, R., Costanzo, E., Luca, A. D., Giavaresi, G., Fontana, S., & Alessandro, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512046 · Cited by 258
Macrophage autophagy in macrophage polarization, chronic inflammation and organ fibrosis
Wen, J.-H., Li, D.-Y., Liang, S., Yang, C., Tang, J., & Liu, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.946832 · Cited by 219
Patient-derived organoids in precision cancer medicine
Tong, L., Cui, W., Zhang, B., Fonseca, P., Zhao, Q. C., Zhang, P., Xu, B., Zhang, Q., Li, Z., Seashore-Ludlow, B. A., et al. (2024) · Med · doi:10.1016/j.medj.2024.08.010 · Cited by 192
Recent advances in defined hydrogels in organoid research
Gan, Z., Qin, X., Liu, H., Liu, J., & Qin, J. (2023) · Bioactive Materials · doi:10.1016/j.bioactmat.2023.06.004 · Cited by 138
Metadata
- Authors
- Yi, S. A., Zhang, Y., Rathnam, C., Pongkulapa, T., & Lee, K.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- Corresponding author
- Lee, Ki‐Bum
- Venue
- Advanced Materials
- Publisher
- Wiley
- Published
- 2021-09-24
- Volume
- 33
- Issue
- 45
- Pages
- e2007949-e2007949
- ISSN
- 0935-9648 (ISSN-L)
- 1521-4095
- PMC
- PMC8682947
- OpenAlex
- W3199075493
- Cited by
- 218
- References
- 235
- Citations by year
- 2026: 50 · 2025: 76 · 2024: 53 · 2023: 26 · 2022: 12 · 2021: 1
- FWCI
- 1.95
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Advanced Materials (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Deafness and Other Communication Disorders (R01DC016612)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R21AR071101)
- National Institute of Biomedical Imaging and Bioengineering (T32EB005583)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- organoids, organoid engineering, 3D cell culture, stem cell-derived organoids, extracellular matrix, gene modulation, organogenesis, disease modeling, biomaterials
- MeSH terms
- Cell Culture Techniques, Three Dimensional, Biocompatible Materials, Biomedical Engineering, Extracellular Matrix, Genetic Engineering, Humans, Neoplasms, Organoids, Stem Cells, Hydrogels
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