Literature DB >> 32571167

Engineering Brain-Specific Pericytes from Human Pluripotent Stem Cells.

Richard Jeske1, Jonathan Albo1, Mark Marzano1, Julie Bejoy1, Yan Li1.   

Abstract

Pericytes (PCs) are a type of perivascular cells that surround endothelial cells of small blood vessels. In the brain, PCs show heterogeneity depending on their position within the vasculature. As a result, PC interactions with surrounding endothelial cells, astrocytes, and neuron cells play a key role in a wide array of neurovascular functions such as regulating blood-brain barrier (BBB) permeability, cerebral blood flow, and helping to facilitate the clearance of toxic cellular molecules. Therefore, a reliable method of engineering brain-specific PCs from human induced pluripotent stem cells (hiPSCs) is critical in neurodegenerative disease modeling. This review summarizes brain-specific PC differentiation of hiPSCs through mesoderm and neural crest induction. Key signaling pathways (platelet-derived growth factor-B [PDGF-B], transforming growth factor [TGF]-β, and Notch signaling) regulating PC function, PC interactions with adjacent cells, and PC differentiation from hiPSCs are also discussed. Specifically, PDGF-BB-platelet-derived growth factor receptor β signaling promotes PC cell survival, TGF-β signal transduction facilitates PC attachment to endothelial cells, and Notch signaling is critical in vascular development and arterial-venous specification. Furthermore, current challenges facing the use of hiPSC-derived PCs are discussed, and their ongoing uses in neurodegenerative disease modeling are identified. Further investigations into PCs and surrounding cell interactions are needed to characterize the roles of brain PCs in various neurodegenerative disorders. Impact statement This article summarizes the work related to brain-specific pericytes (PCs) derived from human pluripotent stem cells (hPSCs). In particular, key signaling pathways regulating PC function, PC interactions with adjacent cells, and PC differentiation from hPSCs were discussed. Furthermore, current challenges facing the use of hPSC-derived PCs were identified, and their ongoing uses in neurodegenerative disease modeling were discussed. The review highlights the important role of cell-cell interactions in blood-brain barrier (BBB) models and neurodegeneration. The summarized findings are significant for establishing pluripotent stem cell-based BBB models toward the applications in drug screening and disease modeling.

Entities:  

Keywords:  brain specific; human pluripotent stem cells; mesenchymal stem cells; neuroinflammation; pericytes

Year:  2020        PMID: 32571167      PMCID: PMC7462039          DOI: 10.1089/ten.TEB.2020.0091

Source DB:  PubMed          Journal:  Tissue Eng Part B Rev        ISSN: 1937-3368            Impact factor:   6.389


  138 in total

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Journal:  Nature       Date:  2018-02-14       Impact factor: 49.962

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Authors:  Leon C D Smyth; Justin Rustenhoven; Thomas I-H Park; Patrick Schweder; Deidre Jansson; Peter A Heppner; Simon J O'Carroll; Edward W Mee; Richard L M Faull; Maurice Curtis; Mike Dragunow
Journal:  J Neuroinflammation       Date:  2018-05-11       Impact factor: 8.322

10.  Specification and Diversification of Pericytes and Smooth Muscle Cells from Mesenchymoangioblasts.

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Journal:  Cell Rep       Date:  2017-05-30       Impact factor: 9.423

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2.  In Vitro Culture Expansion Shifts the Immune Phenotype of Human Adipose-Derived Mesenchymal Stem Cells.

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Review 3.  Neural crest cell-derived pericytes act as pro-angiogenic cells in human neocortex development and gliomas.

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Review 4.  Dynamic 3D On-Chip BBB Model Design, Development, and Applications in Neurological Diseases.

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Review 5.  Recent progress and new challenges in modeling of human pluripotent stem cell-derived blood-brain barrier.

Authors:  Li Yan; Rebecca A Moriarty; Kimberly M Stroka
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  6 in total

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