PMID- 33743764 OWN - NLM STAT- MEDLINE DCOM- 20211109 LR - 20211109 IS - 2045-8118 (Electronic) IS - 2045-8118 (Linking) VI - 18 IP - 1 DP - 2021 Mar 20 TI - Neural crest cell-derived pericytes act as pro-angiogenic cells in human neocortex development and gliomas. PG - 14 LID - 10.1186/s12987-021-00242-7 [doi] LID - 14 AB - Central nervous system diseases involving the parenchymal microvessels are frequently associated with a 'microvasculopathy', which includes different levels of neurovascular unit (NVU) dysfunction, including blood-brain barrier alterations. To contribute to the understanding of NVU responses to pathological noxae, we have focused on one of its cellular components, the microvascular pericytes, highlighting unique features of brain pericytes with the aid of the analyses carried out during vascularization of human developing neocortex and in human gliomas. Thanks to their position, centred within the endothelial/glial partition of the vessel basal lamina and therefore inserted between endothelial cells and the perivascular and vessel-associated components (astrocytes, oligodendrocyte precursor cells (OPCs)/NG2-glia, microglia, macrophages, nerve terminals), pericytes fulfil a central role within the microvessel NVU. Indeed, at this critical site, pericytes have a number of direct and extracellular matrix molecule- and soluble factor-mediated functions, displaying marked phenotypical and functional heterogeneity and carrying out multitasking services. This pericytes heterogeneity is primarily linked to their position in specific tissue and organ microenvironments and, most importantly, to their ontogeny. During ontogenesis, pericyte subtypes belong to two main embryonic germ layers, mesoderm and (neuro)ectoderm, and are therefore expected to be found in organs ontogenetically different, nonetheless, pericytes of different origin may converge and colonize neighbouring areas of the same organ/apparatus. Here, we provide a brief overview of the unusual roles played by forebrain pericytes in the processes of angiogenesis and barriergenesis by virtue of their origin from midbrain neural crest stem cells. A better knowledge of the ontogenetic subpopulations may support the understanding of specific interactions and mechanisms involved in pericyte function/dysfunction, including normal and pathological angiogenesis, thereby offering an alternative perspective on cell subtype-specific therapeutic approaches. FAU - Girolamo, Francesco AU - Girolamo F AUID- ORCID: 0000-0001-8706-3386 AD - Department of Basic Medical Sciences, Neuroscience and Sensory Organs, Human Anatomy and Histology Unit, University of Bari School of Medicine, Bari, Italy. fgirolamo13@gmail.com. FAU - de Trizio, Ignazio AU - de Trizio I AD - Department of Basic Medical Sciences, Neuroscience and Sensory Organs, Human Anatomy and Histology Unit, University of Bari School of Medicine, Bari, Italy. AD - Intensive Care Unit, Department of Intensive Care, Regional Hospital of Lugano, Ente Ospedaliero Cantonale, Lugano, Switzerland. FAU - Errede, Mariella AU - Errede M AD - Department of Basic Medical Sciences, Neuroscience and Sensory Organs, Human Anatomy and Histology Unit, University of Bari School of Medicine, Bari, Italy. FAU - Longo, Giovanna AU - Longo G AD - Department of Basic Medical Sciences, Neuroscience and Sensory Organs, Molecular Biology Unit, University of Bari School of Medicine, Bari, Italy. FAU - d'Amati, Antonio AU - d'Amati A AD - Department of Basic Medical Sciences, Neuroscience and Sensory Organs, Human Anatomy and Histology Unit, University of Bari School of Medicine, Bari, Italy. AD - Department of Emergency and Organ Transplantation, Pathology Section, University of Bari School of Medicine, Bari, Italy. FAU - Virgintino, Daniela AU - Virgintino D AD - Department of Basic Medical Sciences, Neuroscience and Sensory Organs, Human Anatomy and Histology Unit, University of Bari School of Medicine, Bari, Italy. LA - eng PT - Journal Article PT - Review DEP - 20210320 PL - England TA - Fluids Barriers CNS JT - Fluids and barriers of the CNS JID - 101553157 SB - IM MH - Glioma/*physiopathology MH - Humans MH - Neocortex/*blood supply/*growth & development MH - Neovascularization, Pathologic/*physiopathology MH - Neovascularization, Physiologic/*physiology MH - Neural Crest/*cytology MH - Pericytes/*physiology PMC - PMC7980348 OTO - NOTNLM OT - Angiogenesis OT - Blood-brain barrier OT - Human brain development OT - Human gliomas OT - Microvessels OT - Neural crest cells OT - Pericytes OT - Prosencephalon OT - Tunnelling nanotubes COIS- All the authors declare that they have no competing interests. EDAT- 2021/03/22 06:00 MHDA- 2021/11/10 06:00 PMCR- 2021/03/20 CRDT- 2021/03/21 20:34 PHST- 2020/09/28 00:00 [received] PHST- 2021/02/13 00:00 [accepted] PHST- 2021/03/21 20:34 [entrez] PHST- 2021/03/22 06:00 [pubmed] PHST- 2021/11/10 06:00 [medline] PHST- 2021/03/20 00:00 [pmc-release] AID - 10.1186/s12987-021-00242-7 [pii] AID - 242 [pii] AID - 10.1186/s12987-021-00242-7 [doi] PST - epublish SO - Fluids Barriers CNS. 2021 Mar 20;18(1):14. doi: 10.1186/s12987-021-00242-7.