Exploring the heterogeneity of perivascular cells
dc.contributor.advisor
Peault, Bruno
dc.contributor.advisor
Gray, Gillian
dc.contributor.author
Casamitjana, Joan
dc.contributor.sponsor
Medical Research Council (MRC)
en
dc.date.accessioned
2022-02-04T09:41:13Z
dc.date.available
2022-02-04T09:41:13Z
dc.date.issued
2021-12-08
dc.description.abstract
Perivascular cells have been identified as in vivo progenitors of mesenchymal stem
cells (MSCs), these being widely used as adult stem cells in multiple clinical conditions. Indeed, pericytes can differentiate into mesodermal lineages when cultured in
induction media. Compared to MSCs, pericytes represent a more refined population
of cells. As the interest to identify and isolate pure populations of pericytes increased,
several markers have simultaneously and independently become reference pericyte
identifiers. Nevertheless, the term “pericyte” exclusively refers to cells in a specific
anatomical position -cells in the perivascular area of small blood vessels and embedded within its basal lamina- and in situ can be found around multiple types of vessels,
in varying morphology and immunophenotype. This heterogeneity is being explored
but remains largely unknown.
To investigate perivascular cell heterogeneity, we have used multiple well established
pericyte markers (CD146, αSMA, NG2, leptin receptor [LepR], PDGFRβ, PDGFRα)
across multiple tissues, including foetal and adult human (heart, skeletal muscle, bone
marrow, subcutaneous white adipose tissue), murine (heart, skeletal muscle) and
porcine tissues (heart, subcutaneous white adipose tissue). Immunohistological analysis was used to identify different pericyte subtypes, as well as their tissue distribution.
Flow cytometry allowed pericyte subtype quantification and, when possible, cell sorting
was performed for subsequent culture. When long-term cell cultures were established,
cell lines at low passages were used in multiple in vitro assays to characterise their
mesenchymal potential, including clonogenesis, growth, migration, metabolic activity or mesodermal cell differentiation ability.
Analysis focused on LepR showed presence of subtypes in the foetal and adult bone
marrow, but when sorted, presented donor-related differences in vitro. Foetal cardiac
histological analysis revealed different distribution of perivascular layers within cardiac
compartments, with homogeneous coverage of PDGFRβ
+ and PDGFRα
+ perivascular layers but significantly different for αSMA+ (p-value<0.0001). Subsets based
on PDGFRβ and PDGFRα were present in both foetal human and adult murine tissues, but when sorted cell cultures were not achieved. NG2+ pericytes presented
high mortality following enzymatical tissue dissociation, but were successfully isolated
and sorted. In vitro, NG2 subtypes presented donor-dependent variations in multiple
assays, but the NG2- subset performed better when results were homogeneous.
Together, this work shows the existence of multiple subtypes within generally assumed
homogeneous pericyte populations. Variability concerns tissue distribution, with respect to the specific marker used, both within a specific tissue and across different
tissues, and in vitro mesenchymal developmental potentials. Also, this work highlights
donor-related differences within human tissues. In addition, current practices and terminology use, or misuse, involving perivascular and mesenchymal cells isolation, cell
culture and later use are discussed.
en
dc.identifier.uri
https://hdl.handle.net/1842/38529
dc.identifier.uri
http://dx.doi.org/10.7488/era/1793
dc.language.iso
en
en
dc.publisher
The University of Edinburgh
en
dc.relation.hasversion
Carolyn A. Meyers, Joan Casamitjana, Leslie Chang, Lei Zhang, Aaron W. James , Bruno Peault. Pericytes for Therapeutic Bone Repair. Adv Exp Med Biol. ´ 2018;1109:21- 32. doi: 10.1007/978-3-030-02601-1 3. In: Birbrair A. (eds) Pericyte Biology - Novel Concepts. Advances in Experimental Medicine and Biology, vol 1109. Springer, Cham
en
dc.relation.hasversion
Diana Sa da Bandeira, Joan Casamitjana, Mihaela Crisan. Pericytes, integral components of adult hematopoietic stem cell niches. Pharmacol Ther. 2017 Mar;171:104- 113. doi: 10.1016/j.pharmthera.2016.11.006. Epub 2016 Nov 28
en
dc.relation.hasversion
Mario Armando Gomez-Salazar, Zaniah Nashira Gonzalez, ´ Joan Casamitjana, Mihaela Crisan, Bruno Peault. Five decades later, are mesenchymal stem cells still ´ relevant? Front. Bioeng. Biotechnol... doi: 10.3389/fbioe.2020.00148
en
dc.relation.hasversion
Bianca Vezzani, Mario Armando Gomez-Salazar, Joan Casamitjana, Carlo Tremolada, Bruno Peault. Human Adipose Tissue Micro-Fragmentation for Cell Phenotyping and Secretome Characterization. J. Vis. Exp. (152), e60117, doi:10.3791/60117 (2019).
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dc.subject
mesenchymal stem cells
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dc.subject
mesenchymal stromal cells
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dc.subject
perivascular cells
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dc.subject
regeneration
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dc.subject
pericyte
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dc.subject
adventitial cell
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dc.title
Exploring the heterogeneity of perivascular cells
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
en
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