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Multipotent mesenchymal stromal cells obtained from diverse human tissues share functional properties and gene-expression profile with CD146(+) perivascular cells and fibroblasts
Open accessAbstract
Objective The relationship of multipotent mesenchymal stromal cells (MSC) with pericytes and fibroblasts has not been established thus far, although they share many markers of primitive marrow stromal cells and the osteogenic, adipogenic, and chondrogenic differentiation potentials.Materials and methods We compared MSCs from adult or fetal tissues, MSC differentiated in vitro, fibroblasts and cultures of retinal pericytes obtained either by separation with anti-CD146 or adhesion. The characterizations included morphological, immunophenotypic, gene-expression profile, and differentiation potential.Results Osteogenic, adipocytic, and chondrocytic differentiation was demonstrated for MSC, retinal perivascular cells, and fibroblasts. Cell morphology and the phenotypes defined by 22 markers were very similar. Analysis of the global gene expression obtained by serial analysis of gene expression for 17 libraries and by reverse transcription polymerase chain reaction of 39 selected genes from 31 different cell cultures, revealed similarities among MSC, retinal perivascular cells, and hepatic stellate cells. Despite this overall similarity, there was a heterogeneous expression of genes related to angiogenesis, in MSC derived from veins, artery, perivascular cells, and fibroblasts. Evaluation of typical pericyte and MSC transcripts, such as NG2, CD146, CD271, and CD140B on CD146 selected perivascular cells and MSC by real-time polymerase chain reaction confirm the relationship between these two cell types. Furthermore, the inverse correlation between fibroblast-specific protein-1 and CD146 transcripts observed on pericytes, MSC, and fibroblasts highlight their potential use as markers of this differentiation pathway.Conclusion Our results indicate that human MSC and pericytes are similar cells located in the wall of the vasculature, where they function as cell sources for repair and tissue maintenance, whereas fibroblasts are more differentiated cells with more restricted differentiation potential.
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Cell transplantation therapy for diabetes mellitus: endocrine pancreas and adipocyte [Review]
Fujikura, J., Hosoda, K., & Nakao, K. (2013) · Endocrine Journal · doi:10.1507/endocrj.ej13-0162 · Cited by 3
Isolation of CD146+ Resident Lung Mesenchymal Stromal Cells from Rat Lungs
Collins, J. J. P., Möbius, M. A., & Thébaud, B. (2016) · Journal of Visualized Experiments · doi:10.3791/53782 · Cited by 3
Mesenchymal Stem Cells: An Optimistic Cell Source in Tissue Engineering for Bone Regeneration
Hosseini, S., & Eslaminejad, M. B. (2016) · Stem cells in clinical applications · doi:10.1007/978-3-319-40144-7_10 · Cited by 3
Cell based therapeutic approach in vascular surgery: application and review
Rocca, A., Tafuri, D., Paccone, M., Giuliani, A., Zamboli, A. G. I., Surfaro, G., Paccone, A., Compagna, R., Amato, M., Serra, R., et al. (2017) · Open Medicine · doi:10.1515/med-2017-0045 · Cited by 3
“Important elements of AA are represented by chronic inflammation of the aortic wall induced by chemokines and aortic ECM degradation by MMP-2 and MMP-9, so MSCs that migrate toward MMPs and Chemokines can be useful for therapy of aortic aneurysm [222-225].”
BackgroundOrigin of tendon stem cells in situ
Harvey, T., & Fan, C. (2018) · Frontiers in Biology · doi:10.1007/s11515-018-1504-4 · Cited by 3
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Review and prospect of CD146 research
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High-density Lipoproteins Induce the Migration Capacity of Mesenchymal Stromal Cells
Spillmann, F. (2014) · Journal of Stem Cell Research & Therapy · doi:10.4172/2157-7633.1000176 · Cited by 2
“Therefore, we suggest that the HDLand apo A-I-induced improvement in MSC functionality facilitates circulating MSC to migrate towards the site of injury and to contribute to endothelial repair via their ability to render endothelial cells support as pericyte-like cell [41] and their capacity to induce angiogenesis in…”
BackgroundComparative study of bone marrow mesenchymal stromal cells at different stages of ontogeny
Payushina, O. V., Butorina, N. N., Шевелева, О. Н., Bukhinnik, S. S., Berezina, A. A., Ramazanova, S. G., & Domaratskaya, E. I. (2017) · Russian Journal of Developmental Biology · doi:10.1134/s1062360417040087 · Cited by 2
“Cells with the properties of MSCs are found in the majority of tissues and organs (da Silva Meirelles et al., 2006; Covas et al., 2008).”
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Use of Cancer/Testis Antigens in Immunotherapy: Potential Effect on Mesenchymal Stem Cells
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“With this combination of mAbs we guaranteed the identification of a welldefined EC population by their typical CD45- CD146+brightCD31+bright staining and we were able to exclude most of the cell populations that could be misinterpreted as EC, such as CD45+brightCD146+ lymphocyte subsets, perivascular cells, including…”
Mesenchymal Stem Cells During Tumor Formation and Dissemination
Correa, D. (2016) · Current Stem Cell Reports · doi:10.1007/s40778-016-0046-4 · Cited by 2
Analysis of TNF-alpha-Mediated Cerebral Pericyte Remodeling
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Enhancing the Potency of Mesenchymal Stem Cells for Tissue Regeneration
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“[172-174]”
Similarities and Differences in Stem Cells Between Cancer, Normal, and Injured Brain
Huang, L. H., & Huang, P. (2016) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-46733-7_5 · Cited by 2
Mesenchymal stromal cells as a resource for regeneration of damaged skin
Domaratskaya, E. I., & Payushina, O. V. (2017) · Biology Bulletin Reviews · doi:10.1134/s207908641704003x · Cited by 2
“Aside from bone marrow, which is their basic source in postnatal ontogenesis, the spleen, thymus, lungs, heart, and blood vessels, as well as bone, fat, muscular, and other tissues, can be alternative sources (da Silva Meirelles et al., 2006; Beltrami et al., 2007; Yoshimura et al., 2007; Covas et al., 2008; Riekstina…”
Background
Metadata
- Authors
- Covas, D. T., Panepucci, R. A., Fontes, A. M., Silva, W. A., Orellana, M. D., Freitas, M. C. C., Neder, L., Santos, A. R. D., Peres, L. C., Jamur, M. C., & Zago, M. A.
- Affiliations
- Universidade de São Paulo (BR)
- Corresponding author
- Covas, Dimas T.
- ORCID
- Venue
- Experimental Hematology
- Publisher
- Elsevier BV
- Published
- 2008-05
- Volume
- 36
- Issue
- 5
- Pages
- 642-654
- ISSN
- 0301-472X (ISSN-L)
- OpenAlex
- W1979782761
- Cited by
- 610
- References
- 93
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 15 · 2023: 14 · 2022: 19 · 2021: 25 · 2020: 31 · 2019: 31 · 2018: 32 · 2017: 32 · 2016: 48 · 2015: 58 · 2014: 49 · 2013: 60 · 2012: 63
- FWCI
- 18.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Experimental Hematology (publishedVersion)
- PubMed (publishedVersion)
- Scientific Electronic Library Online (São Paulo Research Foundation, Latin American and Caribbean Center on Health Sciences Information, Conselho Nacional de Desenvolvimento Científico e Tecnológico) (publishedVersion)
- Funders
- Scheme for Promotion of Academic and Research Collaboration
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Health Sciences › Dentistry › Periodontics › Periodontal Regeneration and Treatments
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Keywords
- mesenchymal stem cells, pericytes, fibroblasts, CD146, hepatic stellate cells, gene expression profiling, osteogenic differentiation, adipogenesis, chondrogenic differentiation, angiogenesis, S100A4, NG2, p75 neurotrophin receptor, PDGFRβ, vascular wall cells, tissue repair
- MeSH terms
- Cell Differentiation, Cell Separation, Cells, Cultured, Fibroblasts, Flow Cytometry, Humans, Transcription, Genetic, Umbilical Cord, Cluster Analysis, Immunophenotyping, Reverse Transcriptase Polymerase Chain Reaction, Pericytes, Gene Expression Profiling, CD146 Antigen, Mesenchymal Stem Cells
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