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Comparison of skeletal and soft tissue pericytes identifies CXCR4 + bone forming mural cells in human tissues.

Authors :
Xu J
Li D
Hsu CY
Tian Y
Zhang L
Wang Y
Tower RJ
Chang L
Meyers CA
Gao Y
Broderick K
Morris C
Hooper JE
Nimmagadda S
Péault B
James AW
Source :
Bone research [Bone Res] 2020 May 22; Vol. 8 (1), pp. 22. Date of Electronic Publication: 2020 May 22 (Print Publication: 2020).
Publication Year :
2020

Abstract

Human osteogenic progenitors are not precisely defined, being primarily studied as heterogeneous multipotent cell populations and termed mesenchymal stem cells (MSCs). Notably, select human pericytes can develop into bone-forming osteoblasts. Here, we sought to define the differentiation potential of CD146 <superscript>+</superscript> human pericytes from skeletal and soft tissue sources, with the underlying goal of defining cell surface markers that typify an osteoblastogenic pericyte. CD146 <superscript>+</superscript> CD31 <superscript>-</superscript> CD45 <superscript>-</superscript> pericytes were derived by fluorescence-activated cell sorting from human periosteum, adipose, or dermal tissue. Periosteal CD146 <superscript>+</superscript> CD31 <superscript>-</superscript> CD45 <superscript>-</superscript> cells retained canonical features of pericytes/MSC. Periosteal pericytes demonstrated a striking tendency to undergo osteoblastogenesis in vitro and skeletogenesis in vivo, while soft tissue pericytes did not readily. Transcriptome analysis revealed higher CXCR4 signaling among periosteal pericytes in comparison to their soft tissue counterparts, and CXCR4 chemical inhibition abrogated ectopic ossification by periosteal pericytes. Conversely, enrichment of CXCR4 <superscript>+</superscript> pericytes or stromal cells identified an osteoblastic/non-adipocytic precursor cell. In sum, human skeletal and soft tissue pericytes differ in their basal abilities to form bone. Diversity exists in soft tissue pericytes, however, and CXCR4 <superscript>+</superscript> pericytes represent an osteoblastogenic, non-adipocytic cell precursor. Indeed, enrichment for CXCR4-expressing stromal cells is a potential new tactic for skeletal tissue engineering.<br />Competing Interests: Competing interestsA.W.J. is on the scientific advisory board for Novadip Biosciences, receives funding for unrelated research from MTF Biologics, and is on the editorial board of American Journal of Pathology and Bone Research. B.P. is the inventor of perivascular stem cell-related patents held by the UC Regents and is on the editorial board of Stem Cells.<br /> (© The Author(s) 2020.)

Details

Language :
English
ISSN :
2095-4700
Volume :
8
Issue :
1
Database :
MEDLINE
Journal :
Bone research
Publication Type :
Academic Journal
Accession number :
32509378
Full Text :
https://doi.org/10.1038/s41413-020-0097-0