Brain Pericytes As Mediators of Neuroinflammation

Neurovascular pathways to neurodegeneration in Alzheimer’s disease and other disorders

Zlokovic, B. V. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3114 · Cited by 2,969 · 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

Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises

Armulik, A., Genové, G., & Betsholtz, C. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.07.001 · Cited by 2,653 · see citing works

Identification of a unique TGF-β–dependent molecular and functional signature in microglia

Butovsky, O., Jedrychowski, M. P., Moore, C. S., Cialic, R., Lanser, A. J., Gabriely, G., Koeglsperger, T., Dake, B., Wu, P. M., Doykan, C. E., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3599 · Cited by 2,543 · see citing works

Blood-brain barrier breakdown in the aging human hippocampus

Montagne, A., Barnes, S. R., Sweeney, M. D., Halliday, M. R., Sagare, A. P., Zhao, Z., Toga, A. W., Jacobs, R. E., Liu, C. Y., Amezcua, L., et al. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.032 · Cited by 2,102 · see citing works

Capillary pericytes regulate cerebral blood flow in health and disease

Hall, C. N., Reynell, C., Gesslein, B., Hamilton, N. B., Mishra, A., Sutherland, B. A., O’Farrell, F. M., Buchan, A. M., Lauritzen, M., & Attwell, D. (2014) · Nature · doi:10.1038/nature13165 · Cited by 1,870 · see citing works

Control of microglial neurotoxicity by the fractalkine receptor

Cardona, A. E., Pioro, E. P., Sasse, M. E., Kostenko, V., Cardona, S. M., Dijkstra, I. M., Huang, D., Kidd, G., Dombrowski, S., Dutta, R., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1715 · Cited by 1,531 · see citing works

Pericytes Control Key Neurovascular Functions and Neuronal Phenotype in the Adult Brain and during Brain Aging

Bell, R. D., Winkler, E. A., Sagare, A. P., Singh, I., LaRue, B., Deane, R., & Zlokovic, B. V. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.043 · Cited by 1,448 · see citing works

Clearance of Alzheimer’s amyloid-β1-40 peptide from brain by LDL receptor–related protein-1 at the blood-brain barrier

Shibata, M., Yamada, S., Kumar, S. R., Calero, M., Bading, J., Frangione, B., Holtzman, D. M., Miller, C. A., Strickland, D. K., Ghiso, J., et al. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10498 · Cited by 1,413 · see citing works

Cerebral Arterial Pulsation Drives Paravascular CSF–Interstitial Fluid Exchange in the Murine Brain

Iliff, J. J., Wang, M., Zeppenfeld, D. M., Venkataraman, A., Plog, B. A., Liao, Y., Deane, R., & Nedergaard, M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1592-13.2013 · Cited by 1,319 · see citing works

Tight junctions of the blood-brain barrier: development, composition and regulation.

Wolburg, H., & Lippoldt, A. (2002) · PubMed · doi:10.1016/s1537-1891(02)00200-8 · Cited by 1,184 · see citing works

Pericytes of the neurovascular unit: key functions and signaling pathways

Sweeney, M. D., Ayyadurai, S., & Zlokovic, B. V. (2016) · Nature Neuroscience · doi:10.1038/nn.4288 · Cited by 1,125 · see citing works

Cerebral microvascular pathology in aging and Alzheimer's disease

Farkas, E., & Luiten, P. G. M. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00068-x · Cited by 1,102 · see citing works

Three or more routes for leukocyte migration into the central nervous system

Ransohoff, R. M., Kivisäkk, P., & Kidd, G. (2003) · Nature Reviews Immunology · doi:10.1038/nri1130 · Cited by 1,052 · see citing works

Central nervous system pericytes in health and disease

Winkler, E. A., Bell, R. D., & Zlokovic, B. V. (2011) · Nature Neuroscience · doi:10.1038/nn.2946 · Cited by 962 · see citing works

Glioblastoma Stem Cells Generate Vascular Pericytes to Support Vessel Function and Tumor Growth

Cheng, L., Huang, Z., Zhou, W., Wu, Q., Donnola, S., Liu, J. K., Fang, X., Sloan, A. E., Mao, Y., Lathia, J. D., et al. (2013) · Cell · doi:10.1016/j.cell.2013.02.021 · Cited by 905 · see citing works

A Pericyte Origin of Spinal Cord Scar Tissue

Göritz, C., Dias, D. O., Tomilin, N., Barbacid, M., Shupliakov, O., & Frisén, J. (2011) · Science · doi:10.1126/science.1203165 · Cited by 858 · see citing works

LRP/Amyloid β-Peptide Interaction Mediates Differential Brain Efflux of Aβ Isoforms

Deane, R., Wu, Z., Sagare, A., Davis, J., Du Yan, S., Hamm, K., Xu, F., Parisi, M., LaRue, B., Hu, H. W., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.07.017 · Cited by 828 · see citing works

Cyclooxygenase-2 (COX-2) in Inflammatory and Degenerative Brain Diseases

Minghetti, L. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.9.901 · Cited by 780 · see citing works

apoE isoform–specific disruption of amyloid β peptide clearance from mouse brain

Deane, R., Sagare, A., Hamm, K., Parisi, M., Lane, S., Finn, M. B., Holtzman, D. M., & Zlokovic, B. V. (2008) · Journal of Clinical Investigation · doi:10.1172/jci36663 · Cited by 771 · see citing works

Solutes, but not cells, drain from the brain parenchyma along basement membranes of capillaries and arteries: significance for cerebral amyloid angiopathy and neuroimmunology

Carare, R. O., Bernardes‐Silva, M., Newman, T. A., Page, A. M., Nicoll, J. A. R., Perry, V. H., & Weller, R. O. (2008) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2007.00926.x · Cited by 665 · see citing works

Accelerated pericyte degeneration and blood–brain barrier breakdown in apolipoprotein E4 carriers with Alzheimer’s disease

Halliday, M. R., Rege, S. V., Ma, Q., Zhao, Z., Miller, C. A., Winkler, E. A., & Zlokovic, B. V. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.44 · Cited by 649 · see citing works

What is a pericyte?

Attwell, D., Mishra, A., Hall, C. N., O’Farrell, F. M., & Dalkara, T. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15610340 · Cited by 648 · see citing works

Blood-Brain Barrier Leakage in Patients with Early Alzheimer Disease

van de Haar, H. J., Burgmans, S., Jansen, J. F. A., van Osch, M. J. P., van Buchem, M. A., Muller, M., Hofman, P. A. M., Verhey, F. R. J., & Backes, W. H. (2016) · Radiology · doi:10.1148/radiol.2016152244 · Cited by 601 · see citing works

Sall1 is a transcriptional regulator defining microglia identity and function

Buttgereit, A., Lelios, I., Yu, X., Vrohlings, M., Krakoski, N. R., Gautier, E. L., Nishinakamura, R., Becher, B., & Greter, M. (2016) · Nature Immunology · doi:10.1038/ni.3585 · Cited by 570 · see citing works

Fibrinogen-induced perivascular microglial clustering is required for the development of axonal damage in neuroinflammation

Davalos, D., Kyu Ryu, J., Merlini, M., Baeten, K. M., Le Moan, N., Petersen, M. A., Deerinck, T. J., Smirnoff, D. S., Bedard, C., Hakozaki, H., et al. (2012) · Nature Communications · doi:10.1038/ncomms2230 · Cited by 568 · see citing works

Deficiency in Mural Vascular Cells Coincides with Blood–Brain Barrier Disruption in <scp>A</scp> lzheimer's Disease

Sengillo, J. D., Winkler, E. A., Walker, C. T., Sullivan, J. S., Johnson, M., & Zlokovic, B. V. (2013) · Brain Pathology · doi:10.1111/bpa.12004 · Cited by 553 · see citing works

Microvascular injury and blood–brain barrier leakage in Alzheimer's disease

Zipser, B. D., Johanson, C. E., Gonzalez, L., Berzin, T. M., Tavares, R., Hulette, C. M., Vitek, M. P., Hovanesian, V., & Stopa, E. G. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.05.016 · Cited by 487 · see citing works

Pericytes support neutrophil subendothelial cell crawling and breaching of venular walls in vivo

Pröbstl, D., Voisin, M.-B., Woodfin, A., Whiteford, J. R., D’Acquisto, F., Jones, G. E., Rowe, D. W., & Nourshargh, S. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20111622 · Cited by 467 · see citing works

Capillary and arteriolar pericytes attract innate leukocytes exiting through venules and 'instruct' them with pattern-recognition and motility programs

Stark, K., Eckart, A., Haidari, S., Tirniceriu, A., Lorenz, M., von Brühl, M.-L., Gärtner, F., Khandoga, A. G., Legate, K. R., Pless, R., et al. (2013) · Nature Immunology · doi:10.1038/ni.2477 · Cited by 447 · see citing works

Venular basement membranes contain specific matrix protein low expression regions that act as exit points for emigrating neutrophils

Wang, S., Voisin, M.-B., Larbi, K. Y., Dangerfield, J. A., Scheiermann, C., Tran, M. G. B., Maxwell, P. H., Sorokin, L. M., & Nourshargh, S. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20051210 · Cited by 374 · see citing works

IL-33 ameliorates Alzheimer's disease-like pathology and cognitive decline

Fu, A. K. Y., Hung, K.-W., Yuen, M. Y. F., Zhou, X., Mak, D. S. Y., Chan, I. C. W., Cheung, T. H., Zhang, B., Fu, W.-Y., Liew, F. Y., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1604032113 · Cited by 369 · see citing works

Blood–spinal cord barrier breakdown and pericyte reductions in amyotrophic lateral sclerosis

Winkler, E. A., Sengillo, J. D., Sullivan, J. S., Henkel, J. S., Appel, S. H., & Zlokovic, B. V. (2013) · Acta Neuropathologica · doi:10.1007/s00401-012-1039-8 · Cited by 354 · see citing works

Perivascular Spaces and the Two Steps to Neuroinflammation

Owens, T., Bechmann, I., & Engelhardt, B. (2008) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31818f9ca8 · Cited by 352 · see citing works

Lipopolysaccharide Activates Toll-like Receptor 4 (TLR4)-mediated NF-κB Signaling Pathway and Proinflammatory Response in Human Pericytes

Guijarro-Muñoz, I., Compte, M., Álvarez-Cienfuegos, A., Álvarez-Vallina, L., & Sanz, L. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.521161 · Cited by 342 · see citing works

Non-alcoholic fatty liver disease induces signs of Alzheimer’s disease (AD) in wild-type mice and accelerates pathological signs of AD in an AD model

Kim, D.-G., Krenz, A., Toussaint, L. E., Maurer, K. J., Robinson, S.-A., Yan, A., Torres, L., & Bynoe, M. S. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0467-5 · Cited by 330 · see citing works

Matrix Metalloproteinase-9 Mediates Hypoxia-Induced Vascular Leakage in the Brain via Tight Junction Rearrangement

Bauer, A. T., Bürgers, H. F., Rabie, T., & Marti, H. H. (2009) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.248 · Cited by 325 · see citing works

Fibrin deposition accelerates neurovascular damage and neuroinflammation in mouse models of Alzheimer's disease

Paul, J., Strickland, S., & Melchor, J. P. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070304 · Cited by 319 · see citing works

How microglia kill neurons

Brown, G. C., & Vilalta, A. (2015) · Brain Research · doi:10.1016/j.brainres.2015.08.031 · Cited by 306 · see citing works

Brain macrophages: on the role of pericytes and perivascular cells

Thomas, W. E. (1999) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00024-7 · Cited by 306 · see citing works

Platelet-Derived Growth Factor (PDGF)/PDGF Receptors (PDGFR) Axis as Target for Antitumor and Antiangiogenic Therapy

Raica, M., & Cîmpean, A. M. (2010) · Pharmaceuticals · doi:10.3390/ph3030572 · Cited by 305 · see citing works

Diffusion of Macromolecules in the Brain: Implications for Drug Delivery

Wolak, D. J., & Thorne, R. G. (2013) · Molecular Pharmaceutics · doi:10.1021/mp300495e · Cited by 299 · see citing works

The Pericyte: A Forgotten Cell Type with Important Implications for A lzheimer's Disease?

Winkler, E. A., Sagare, A. P., & Zloković, B. V. (2014) · Brain Pathology · doi:10.1111/bpa.12152 · Cited by 275 · see citing works

Blood coagulation protein fibrinogen promotes autoimmunity and demyelination via chemokine release and antigen presentation

Ryu, J. K., Petersen, M. A., Murray, S. G., Baeten, K. M., Meyer-Franke, A., Chan, J. P., Vagena, E., Bedard, C., Machado, M. R., Coronado, P. E. R., et al. (2015) · Nature Communications · doi:10.1038/ncomms9164 · Cited by 271 · see citing works

Low‐density lipoprotein receptor‐related protein‐1: a serial clearance homeostatic mechanism controlling Alzheimer’s amyloid β‐peptide elimination from the brain

Zlokovic, B. V., Deane, R., Sagare, A. P., Bell, R. D., & Winkler, E. A. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07002.x · Cited by 261 · see citing works

SRF and myocardin regulate LRP-mediated amyloid-β clearance in brain vascular cells

Bell, R. D., Deane, R., Chow, N., Long, X., Sagare, A., Singh, I., Streb, J. W., Guo, H., Rubio, A., Van Nostrand, W., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1819 · Cited by 261 · see citing works

Brain Vascular Pericytes Following Ischemia Have Multipotential Stem Cell Activity to Differentiate Into Neural and Vascular Lineage Cells

Nakagomi, T., Kubo, S., Nakano‐Doi, A., Sakuma, R., Lu, S., Narita, A., Kawahara, M., Taguchi, A., & Matsuyama, T. (2015) · Stem Cells · doi:10.1002/stem.1977 · Cited by 257 · see citing works

The human side of microglia

Smith, A. M., & Dragunow, M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2013.12.001 · Cited by 256 · see citing works

Analysis of the brain mural cell transcriptome

He, L., Vanlandewijck, M., Raschperger, E., Andaloussi Mäe, M., Jung, B., Lebouvier, T., Ando, K., Hofmann, J., Keller, A., & Betsholtz, C. (2016) · Scientific Reports · doi:10.1038/srep35108 · Cited by 233 · see citing works

Brain microvascular pericytes are immunoactive in culture: cytokine, chemokine, nitric oxide, and LRP-1 expression in response to lipopolysaccharide

Kováč, A., Erickson, M. A., & Banks, W. A. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-139 · Cited by 227 · see citing works

Detachment of Brain Pericytes from the Basal Lamina is Involved in Disruption of the Blood–Brain Barrier Caused by Lipopolysaccharide-Induced Sepsis in Mice

Nishioku, T., Dohgu, S., Takata, F., Eto, T., Ishikawa, N., Kodama, K., Nakagawa, S., Yamauchi, A., & Kataoka, Y. (2008) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-008-9322-x · Cited by 210 · see citing works

Neurovascular unit impairment in early Alzheimer's disease measured with magnetic resonance imaging

van de Haar, H. J., Jansen, J. F. A., van Osch, M. J. P., van Buchem, M. A., Muller, M., Wong, S. M., Hofman, P. A. M., Burgmans, S., Verhey, F. R. J., & Backes, W. H. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.06.006 · Cited by 207 · see citing works

Brain pericytes among cells constituting the blood-brain barrier are highly sensitive to tumor necrosis factor-α, releasing matrix metalloproteinase-9 and migrating in vitro

Takata, F., Dohgu, S., Matsumoto, J., Takahashi, H., Machida, T., Wakigawa, T., Harada, E., Miyaji, H., Koga, M., Nishioku, T., et al. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-106 · Cited by 203 · see citing works

TGF-beta1 regulates human brain pericyte inflammatory processes involved in neurovasculature function

Rustenhoven, J., Aalderink, M., Scotter, E. L., Oldfield, R. L., Bergin, P. S., Mee, E. W., Graham, E. S., Faull, R. L. M., Curtis, M. A., Park, T. I.-H., et al. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0503-0 · Cited by 201 · see citing works

Brain pericytes acquire a microglial phenotype after stroke

Özen, Í., Deierborg, T., Miharada, K., Padel, T., Englund, E. M., Genové, G., & Paul, G. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1295-x · Cited by 201 · see citing works

The PDGF-BB-SOX7 axis-modulated IL-33 in pericytes and stromal cells promotes metastasis through tumour-associated macrophages

Yang, Y., Andersson, P., Hosaka, K., Zhang, Y., Cao, R., Iwamoto, H., Yang, X., Nakamura, M., Wang, J., Zhuang, R., et al. (2016) · Nature Communications · doi:10.1038/ncomms11385 · Cited by 185 · see citing works

CNS Microvascular Pericytes Express Macrophage-like Function, Cell Surface Integrin αM, and Macrophage Marker ED-2

Balabanov, R. D., Washington, R. A., Wagnerová, J., & Dore‐Duffy, P. (1996) · Microvascular Research · doi:10.1006/mvre.1996.0049 · Cited by 182 · see citing works

Brain pericytes serve as microglia-generating multipotent vascular stem cells following ischemic stroke

Sakuma, R., Kawahara, M., Nakano‐Doi, A., Takahashi, A., Tanaka, Y., Narita, A., Kuwahara‐Otani, S., Hayakawa, T., Yagi, H., Matsuyama, T., et al. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0523-9 · Cited by 180 · see citing works

A role for human brain pericytes in neuroinflammation

Jansson, D., Rustenhoven, J., Feng, S. X., Hurley, D., Oldfield, R. L., Bergin, P., Mee, E. W., Faull, R. L. M., & Dragunow, M. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-104 · Cited by 168 · see citing works

Rapid Degeneration of Cultured Human Brain Pericytes by Amyloid β Protein

Verbeek, M., de Waal, R., Schipper, J., & Nostrand, W. V. V. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.68031135.x · Cited by 166 · see citing works

Memory CD4 T cells: generation, reactivation and re‐assignment

MacLeod, M. K. L., Kappler, J. W., & Marrack, P. (2010) · Immunology · doi:10.1111/j.1365-2567.2010.03260.x · Cited by 159 · see citing works

Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer’s disease

Dorr, A. E., Sahota, B., Chinta, L. V., Brown, M. E., Lai, A. Y., Ma, K., Hawkes, C. A., McLaurin, J., & Stefanovic, B. (2012) · Brain · doi:10.1093/brain/aws243 · Cited by 153 · see citing works

The Role of Pericytes in Blood-Brain Barrier Function and Stroke

Liu, S., Agalliu, D., Yu, C., & Fisher, M. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212802002706 · Cited by 151 · see citing works

Pericyte MyD88 and IRAK4 control inflammatory and fibrotic responses to tissue injury

Leaf, I. A., Nakagawa, S., Johnson, B. G., Cha, J. J., Mittelsteadt, K., Guckian, K. M., Gomez, I. G., Altemeier, W. A., & Duffield, J. S. (2016) · Journal of Clinical Investigation · doi:10.1172/jci87532 · Cited by 151 · see citing works

Shedding of soluble platelet-derived growth factor receptor-β from human brain pericytes

Sagare, A. P., Sweeney, M. D., Makshanoff, J., & Zlokovic, B. V. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.09.025 · Cited by 142 · see citing works

Venular Basement Membranes Ubiquitously Express Matrix Protein Low-Expression Regions

Voisin, M.-B., Pröbstl, D., & Nourshargh, S. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2010.090510 · Cited by 141 · see citing works

Brain capillary pericytes contribute to the immune defense in response to cytokines or LPS in vitro

Pieper, C., Marek, J. J., Unterberg, M., Schwerdtle, T., & Galla, H. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.004 · Cited by 132 · see citing works

Cerebrovascular Permeability to Peptides: Manipulations of Transport Systems at the Blood-Brain Barrier

Zloković, B. V. (1995) · Pharmaceutical Research · doi:10.1023/a:1016254514167 · Cited by 131 · see citing works

IL-17 Promotes Neutrophil-Mediated Immunity by Activating Microvascular Pericytes and Not Endothelium

Liu, R., Lauridsen, H. M., Amezquita, R. A., Pierce, R. W., Jane‐wit, D., Fang, C., Pellowe, A. S., Kirkiles-Smith, N. C., Gonzalez, A. L., & Pober, J. S. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600138 · Cited by 122 · see citing works

Relationship between cyclophilin a levels and matrix metalloproteinase 9 activity in cerebrospinal fluid of cognitively normal apolipoprotein e4 carriers and blood-brain barrier breakdown

Halliday, M. R., Pomara, N., Sagare, A. P., Mack, W. J., Frangione, B., & Zlokovic, B. V. (2013) · JAMA Neurology · doi:10.1001/jamaneurol.2013.3841 · Cited by 119 · see citing works

Transport of Leucine‐Enkephalin Across the Blood‐Brain Barrier in the Perfused Guinea Pig Brain

Zloković, B. V., Lipovac, M. N., Begley, D. J., Davson, H., & Rakić, L. (1987) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1987.tb03431.x · Cited by 118 · see citing works

Mesenchymal Stem Cells and Pericytes: To What Extent Are They Related?

de Souza, L. E. B., Malta, T. M., Kashima, S. H., & Covas, D. T. (2016) · Stem Cells and Development · doi:10.1089/scd.2016.0109 · Cited by 117 · see citing works

Dysfunction of brain pericytes in chronic neuroinflammation

Persidsky, Y., Hill, J., Zhang, M., Dykstra, H., Winfield, M., Reichenbach, N. L., Potula, R., Mukherjee, A., Ramirez, S. H., & Rom, S. (2016) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1177/0271678x15606149 · Cited by 116 · see citing works

Pericytes support neutrophil transmigration via interleukin-8 across a porcine co-culture model of the blood–brain barrier

Pieper, C., Pieloch, P., & Galla, H. (2013) · Brain Research · doi:10.1016/j.brainres.2013.05.047 · Cited by 103 · see citing works

T lymphocyte adhesion to human brain pericytes is mediated via very late antigen-4/vascular cell adhesion molecule-1 interactions.

Verbeek, M. M., Westphal, J. R., Ruiter, D. J., & de Waal, R. M. W. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.154.11.5876 · Cited by 103 · see citing works

Vascular Endothelial Growth Factors Enhance the Permeability of the Mouse Blood-brain Barrier

Jiang, S., Xia, R., Jiang, Y., Wang, L., & Gao, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086407 · Cited by 100 · see citing works

Kinetics of arginine-vasopressin uptake at the blood-brain barrier

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Immature mesenchymal stem cell-like pericytes as mediators of immunosuppression in human malignant glioma

Ochs, K., Sahm, F., Opitz, C. A., Lanz, T. V., Oezen, I., Couraud, P., von Deimling, A., Wick, W., & Platten, M. (2013) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2013.09.011 · Cited by 97 · see citing works

Traumatic brain injury results in rapid pericyte loss followed by reactive pericytosis in the cerebral cortex

Zehendner, C. M., Sebastiani, A., Hugonnet, A. V., Bischoff, F. C., Luhmann, H. J., & Thal, S. C. (2015) · Scientific Reports · doi:10.1038/srep13497 · Cited by 97 · see citing works

Tumor necrosis factor-α-stimulated brain pericytes possess a unique cytokine and chemokine release profile and enhance microglial activation

Matsumoto, J., Takata, F., Machida, T., Takahashi, H., Soejima, Y., Funakoshi, M., Futagami, K., Yamauchi, A., Dohgu, S., & Kataoka, Y. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.06.052 · Cited by 95 · see citing works

Cerebrovascular Remodeling and Epilepsy

Marchi, N., & Lerner‐Natoli, M. (2012) · The Neuroscientist · doi:10.1177/1073858412462747 · Cited by 90 · see citing works

Regulation of the blood–brain barrier integrity by pericytes via matrix metalloproteinases mediated activation of vascular endothelial growth factor in vitro

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