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Extracellular matrix and matrix receptors in blood–brain barrier formation and stroke
Open accessAbstract
The blood–brain barrier (BBB) is formed primarily to protect the brain microenvironment from the influx of plasma components, which may disturb neuronal functions. The BBB is a functional unit that consists mainly of specialized endothelial cells (ECs) lining the cerebral blood vessels, astrocytes, and pericytes. The BBB is a dynamic structure that is altered in neurologic diseases, such as stroke. ECs and astrocytes secrete extracellular matrix (ECM) proteins to generate and maintain the basement membranes (BMs). ECM receptors, such as integrins and dystroglycan, are also expressed at the brain microvasculature and mediate the connections between cellular and matrix components in physiology and disease. ECM proteins and receptors elicit diverse molecular signals that allow cell adaptation to environmental changes and regulate growth and cell motility. The composition of the ECM is altered upon BBB disruption and directly affects the progression of neurologic disease. The purpose of this review is to discuss the dynamic changes of ECM composition and integrin receptor expression that control BBB functions in physiology and pathology. © 2011 Wiley Periodicals, Inc. Develop Neurobiol 71: 1018‐1039, 2011
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“Integrins mediate cell signaling by activating ECM ligands, growth factors, and growth factor receptors, which regulates multiple endothelial cell functions including survival, migration, differentiation, adhesion, and polarity (35).”
From Blood-Brain Barrier: From Physiology to Disease and Back (2019) · cites this paper as [35]
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Integrins: Versatility, modulation, and signaling in cell adhesion
Hynes, R. O. (1992) · Cell · doi:10.1016/0092-8674(92)90115-s · Cited by 9,857
Hynes (2002) · doi:10.1016/s0092-8674(02)00971-6 · Cited by 8,606
Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827
Astrocyte-endothelial interactions at the blood-brain barrier
Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595
Astrocytes: Biology and pathology
Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196
Getting to the site of inflammation: the leukocyte adhesion cascade updated
Ley, K., Laudanna, C., Cybulsky, M. I., & Nourshargh, S. (2007) · Nature Reviews Immunology · doi:10.1038/nri2156 · Cited by 4,354
Giancotti, F. G., & Ruoslahti, E. (1999) · Science · doi:10.1126/science.285.5430.1028 · Cited by 3,869
The Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders
Zlokovic, B. V. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.003 · Cited by 3,280
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
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
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Li, Y., Wu, P., Bihl, J. C., & Shi, H. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200106154203 · Cited by 54
Anwar, M. M., Özkan, E., & Özdemir, Y. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15372 · Cited by 58
Laminin regulates oligodendrocyte development and myelination
Kang, M., & Yao, Y. (2021) · Glia · doi:10.1002/glia.24117 · Cited by 56
Biomaterial Applications in Cell‐Based Therapy in Experimental Stroke
Boisserand, L. S. B., Kodama, T., Papassin, J., Auzély‐Velty, R., Moisan, A., Rome, C., & Detante, O. (2016) · Stem Cells International · doi:10.1155/2016/6810562 · Cited by 57
Maherally, Z., Fillmore, H. L., Tan, S. L., Tan, S. F., Jassam, S. A., Quack, F., Hatherell, K. E., & Pilkington, G. J. (2017) · The FASEB Journal · doi:10.1096/fj.201700162r · Cited by 54
Mechanosensitive brain tumor cells construct blood-tumor barrier to mask chemosensitivity
Chen, X., Momin, A., Wanggou, S., Wang, X., Min, H.-K., Dou, W., Gong, Z., Chan, J., Dong, W., Fan, J. J., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.007 · Cited by 54
Matrix metalloproteinase 9–mediated intracerebral hemorrhage induced by cerebral amyloid angiopathy
Zhao, L., Arbel‐Ornath, M., Wang, X., Betensky, R. A., Greenberg, S. M., Frosch, M. P., & Bacskai, B. J. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.07.016 · Cited by 52
Aguiar, R. S., Pohl, F. B., de Morais, G. L., Nogueira, F. C. S., de Carvalho, J. B., Guida, L. D. C., Arge, L. W. P., Melo, A., Moreira, M. E. L., Cunha, D. P., et al. (2020) · Science Signaling · doi:10.1126/scisignal.aay6736 · Cited by 51
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Tibbe, M. P., Leferink, A., van den Berg, A., Eijkel, J. C. T., & Segerink, L. I. (2018) · Advanced Materials Technologies · doi:10.1002/admt.201700200 · Cited by 51
Tissue linkage through adjoining basement membranes: The long and the short term of it
Keeley, D. P., & Sherwood, D. R. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.05.009 · Cited by 46
Labus, J., Wöltje, K., Stolte, K. N., Häckel, S., Kim, K. S., Hildmann, A., & Danker, K. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.10.002 · Cited by 49
A human brain vascular atlas reveals diverse cell mediators of Alzheimer’s disease risk
Yang, A. C., Vest, R. T., Kern, F., Lee, D. P., Maat, C. A., Losada, P. M., Chen, M. B., Agam, M., Schaum, N., Khoury, N., et al. (2021) · doi:10.1101/2021.04.26.441262 · Cited by 48
Gather wisdom to overcome barriers: Well-designed nano-drug delivery systems for treating gliomas
Cui, J., Xu, Y., Tu, H., Zhao, H., Wang, H., Di, L., & Wang, R. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.08.013 · Cited by 47
Badaut, J., & Bix, G. J. (2013) · Translational Stroke Research · doi:10.1007/s12975-013-0304-z · Cited by 48
Targeted Brain Delivery Nanoparticles for Malignant Gliomas
Pinto, M. P., Arce, M., Yameen, B., & Vilos, C. (2016) · Nanomedicine · doi:10.2217/nnm-2016-0307 · Cited by 49
Amruta, N., & Bix, G. J. (2021) · Inflammation · doi:10.1007/s10753-021-01509-9 · Cited by 44
Zang, N., Lin, Z., Huang, K., Pan, Y., Wu, Y., Wu, Y., Wang, S., Wang, D., Ji, Z., & Pan, S. (2020) · Cerebrovascular Diseases · doi:10.1159/000510804 · Cited by 46
Role of Intermediate Filaments in Blood–Brain Barrier in Health and Disease
Bayır, E., & Şendemir, A. (2021) · Cells · doi:10.3390/cells10061400 · Cited by 47
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Payne, L. B., Hoque, M. M., Houk, C., Darden, J. A., & Chappell, J. C. (2020) · Current Tissue Microenvironment Reports · doi:10.1007/s43152-020-00014-9 · Cited by 46
Bansode, S. B., & Gacche, R. N. (2019) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2019.08.004 · Cited by 47
Willis, C. L., Camire, R. B., Brule, S. A., & Ray, D. E. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.06.061 · Cited by 43
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Lauschke, K., Frederiksen, L., & Hall, V. J. (2017) · Stem Cells and Development · doi:10.1089/scd.2017.0003 · Cited by 46
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Fakhoury, M. (2016) · Journal of Neurology · doi:10.1007/s00415-016-8052-0 · Cited by 43
Benarroch, E. E. (2012) · Neurology · doi:10.1212/wnl.0b013e318250d8bc · Cited by 42
Shamul, J. G., Wang, Z., Gong, H., Ou, W., White, A. M., Garcia, D. P. M., Gu, S., Clyne, A. M., Quiñones‐Hinojosa, A., & He, X. (2024) · Nature Biomedical Engineering · doi:10.1038/s41551-024-01250-2 · Cited by 43
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Wang, X., Zhang, M., Feng, R., Li, W., REN, S.-Q., Zhang, J., & Zhang, F. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.030 · Cited by 42
Metabolite transport across the mammalian and insect brain diffusion barriers
Weiler, A., Volkenhoff, A., Hertenstein, H., & Schirmeier, S. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.02.008 · Cited by 46
Keasey, M. P., Kang, S. S., Lovins, C., & Hagg, T. (2013) · Cell Communication and Signaling · doi:10.1186/1478-811x-11-35 · Cited by 40
Jonas, A., Thiem, S., Kuhlmann, T., Wagener, R., Aszódi, A., Nowell, C. J., Hagemeier, K., Laverick, L., Perreau, V. M., Jokubaitis, V., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci71385 · Cited by 38
Pandey, M. K. (2023) · Biomedicines · doi:10.3390/biomedicines11041067 · Cited by 40
Hou, H.-Q., Xiang, X., Pan, Y., Zhang, Q., Li, H., Meng, X., & Wang, Y. (2021) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2021.10.002 · Cited by 38
Kunze, R., & Marti, H. H. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.03.004 · Cited by 38
Wu, C., Chen, M.-C., Liu, S., Yang, T., Long, L.-H., Guan, S., & Chen, C. (2021) · Biomedicines · doi:10.3390/biomedicines9111719 · Cited by 37
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Role of blood–brain barrier dysfunction in the development of poststroke epilepsy
Meijer, W. C., & Gorter, J. A. (2024) · Epilepsia · doi:10.1111/epi.18072 · Cited by 36
Lee, M. J., Choi, J. H., Oh, J., Lee, Y. H., In, J.-G., Chang, B., Nah, S.-Y., & Cho, I. (2020) · Journal of Ginseng Research · doi:10.1016/j.jgr.2020.09.001 · Cited by 36
Structural disruption of the blood–brain barrier in repetitive primary blast injury
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Lei, L., Wang, Y.-T., Hu, D., Gai, C., & Zhang, Y. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01426-5 · Cited by 35
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Tapella, L., Dematteis, G., Moro, M., Pistolato, B., Tonelli, E., Vanella, V. V., Giustina, D., Forgia, A. L., Restelli, E., Barberis, E., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05324-4 · Cited by 34
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Xie, C., Wang, Y., Wang, J., Xu, Y., Liu, H., Guo, J., & Zhu, L. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03041-9 · Cited by 32
Pramotton, F. M., Spitz, S., & Kamm, R. D. (2024) · Advanced Science · doi:10.1002/advs.202403892 · Cited by 33
Moura, R. P., Almeida, A., & Sarmento, B. F. C. C. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.09.001 · Cited by 32
Jensen, L. D., Hot, B., Ramsköld, D., Germano, R. F. V., Yokota, C., Giatrellis, S., Lauschke, V. M., Hubmacher, D., Li, M. X., Hupe, M., et al. (2019) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.119.312388 · Cited by 33
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van Schaik, P. E. M., Zuhorn, I. S., & Baron, W. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158418 · Cited by 35
Kurmann, L., Okoniewski, M. J., & Dubey, R. K. (2021) · Cells · doi:10.3390/cells10071784 · Cited by 30
Aoki, H., Yamashita, M., Hashita, T., Iwao, T., & Matsunaga, T. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00186-4 · Cited by 30
Mazumder, M. K., Bhattacharya, P., & Borah, A. (2014) · Medical Hypotheses · doi:10.1016/j.mehy.2014.09.021 · Cited by 30
Rydbirk, R., Østergaard, O., Folke, J., Hempel, C., DellaValle, B., Andresen, T. L., Løkkegaard, A., Hejl, A., Bode, M., Blaabjerg, M., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04378-z · Cited by 28
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Boeri, L., Perottoni, S., Izzo, L., Giordano, C., & Albani, D. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202002043 · Cited by 28
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Rodriguez‐Grande, B., Ichkova, A., Lemarchant, S., & Badaut, J. (2017) · The AAPS Journal · doi:10.1208/s12248-017-0123-3 · Cited by 29
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Takagi, T., Yoshimura, S., Sakuma, R., Nakano‐Doi, A., Matsuyama, T., & Nakagomi, T. (2017) · Translational Stroke Research · doi:10.1007/s12975-017-0556-0 · Cited by 28
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Nizari, S., Carare, R. O., Romero, I. A., & Hawkes, C. A. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00172 · Cited by 29
Kim, D. Y., Zhang, H., Park, S., Kim, Y., Bae, C., Kim, Y., & Kwon, Y. (2020) · Journal of Molecular Medicine · doi:10.1007/s00109-020-01920-z · Cited by 28
Summers, L., Kangwantas, K., Rodriguez‐Grande, B., Dénes, Á., Penny, J. I., Kielty, C. M., & Pinteaux, E. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.10.007 · Cited by 28
Malik, V. A., & Benedetto, B. D. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00127 · Cited by 31
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Égervári, K., Potter, G., Guzmán-Hernández, M. L., Salmon, P., Soto-Ribeiro, M., Kastberger, B., Balla, T., Wehrle‐Haller, B., & Kiss, J. Z. (2015) · Glia · doi:10.1002/glia.22939 · Cited by 27
Chauhan, P. S., Kumarasamy, M., Carcaboso, A. M., Sosnik, A., & Danino, D. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.112261 · Cited by 27
Lee, M. J., Zhu, J., An, J. H., Lee, S. E., Kim, T. Y., Oh, E., Kang, Y. E., Chung, W., & Heo, J. Y. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-022-00363-7 · Cited by 28
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Hawkins, B. T., Gu, Y.-H., Izawa, Y., & del Zoppo, G. J. (2013) · Brain Research · doi:10.1016/j.brainres.2013.01.049 · Cited by 27
Li, H., Zheng, J., Wang, H., Becker, M. L., & Leipzig, N. D. (2018) · Journal of Biomaterials Applications · doi:10.1177/0885328218755711 · Cited by 27
Raborn, E. S., Jamerson, M., Marciano‐Cabral, F., & Cabral, G. A. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.04.008 · Cited by 27
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Morris, E. K., Daignault, S. M., Stehbens, S. J., Genovesi, L. A., & Lagendijk, A. K. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1101522 · Cited by 28
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Ahmad, N., Kiriako, G., Saliba, J., Abla, K. K., El-Sabban, M. E., & Mhanna, R. (2024) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.4c00599 · Cited by 25
Ahmadpour, D., Mhaouty‐Kodja, S., & Grange‐Messent, V. (2021) · Environmental Research · doi:10.1016/j.envres.2021.112235 · Cited by 25
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Fumagalli, S., Ortolano, F., & Simoni, M. G. D. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.06.005 · Cited by 27
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Saunus, J. M., Reed, A. E. M., Lim, M., & Lakhani, S. R. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010152 · Cited by 25
Ahmadpour, D., & Grange‐Messent, V. (2020) · Neuroendocrinology · doi:10.1159/000509218 · Cited by 22
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Ramiro, L., García‐Berrocoso, T., Briansó, F., Goicoechea, L., Simats, A., Llombart, V., Gonzalo, R., Hainard, A., Martínez-Sáez, E. A., Canals, F., et al. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02401-1 · Cited by 24
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Reichardt, L. F., & Prokop, A. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20975 · Cited by 24
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Han, Y., Sun, Y., Peng, S., Tang, T., Zhang, B., Yu, R., Sun, X., Guo, S., Ma, L., Li, P., et al. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177505 · Cited by 27
Consorti, A., Marco, I. D., & Sansevero, G. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.710303 · Cited by 27
Farhangi, S., Karimi, E., Khajeh, K., Hosseinkhani, S., & Javan, M. (2022) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2022.102609 · Cited by 22
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Liu, H., Qiu, G. P., Zhuo, F., Yu, W. H., Sun, S., Li, F. H., & Yang, M. (2015) · BioMed Research International · doi:10.1155/2015/471631 · Cited by 23
Coelho‐Santos, V., Cardoso, F. L., Magalhães, A., Ferreira-Teixeira, M., Leitão, R. A., Gomes, C. M. F., Rito, M., Barbosa, M., Ribeiro, C., & Silva, A. P. (2018) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2018.12.007 · Cited by 25
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Microvascular networks in the area of the auditory peripheral nervous system
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Metadata
- Authors
- Baeten, K. M., & Akassoglou, K.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Akassoglou, Katerina
- Venue
- Developmental Neurobiology
- Publisher
- Wiley
- Published
- 2011-10-11
- Volume
- 71
- Issue
- 11
- Pages
- 1018-1039
- ISSN
- 1932-8451 (ISSN-L)
- 1932-846X
- PMC
- PMC3482610
- OpenAlex
- W2067935721
- Cited by
- 397
- References
- 232
- Citations by year
- 2026: 8 · 2025: 27 · 2024: 32 · 2023: 48 · 2022: 38 · 2021: 44 · 2020: 39 · 2019: 32 · 2018: 38 · 2017: 22 · 2016: 20 · 2015: 11 · 2014: 14 · 2013: 13 · 2012: 7
- FWCI
- 1.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Developmental Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS066361, R01NS052189, R01NS051470)
- National Center for Research Resources (P41RR004050)
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- blood-brain barrier, extracellular matrix, integrins, dystroglycan, basement membrane, endothelial cells, astrocytes, pericytes, stroke, blood-brain barrier disruption, ECM receptors, cell motility, neurovascular unit
- MeSH terms
- Animals, Blood-Brain Barrier, Brain, Humans, Microcirculation, Receptors, Cell Surface, Extracellular Matrix Proteins, Stroke
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