Modification of the Properties of Extracellular Matrix of Senescent Mesenchymal Stem Cells.


Journal

Bulletin of experimental biology and medicine
ISSN: 1573-8221
Titre abrégé: Bull Exp Biol Med
Pays: United States
ID NLM: 0372557

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 04 04 2023
medline: 9 10 2023
pubmed: 29 9 2023
entrez: 28 9 2023
Statut: ppublish

Résumé

Cell senescence leads to changes in the secretory activity of mesenchymal stem cells (MSC), including proteins of extracellular matrix (ECM). Here we studied the regulatory properties of ECM of senescent MSC in a model with endothelial cells (EC). EC were seeded onto a decellularized extracellular matrix of senescent MSC. Changes in cell morphology and a decrease in cell growth were observed. In addition, increased production of inflammatory chemokines MCP-1 and GROα and reduced synthesis of proangiogenic growth factor FGF-2 were revealed. Analysis of ECM showed quantitative and qualitative changes, including fibronectin layer morphology, total protein content, and concentration of deposited growth factors such as VEGF. Thus, our work demonstrates that senescence of MSC can lead to modification of the effects of their ECM on EC activity.

Identifiants

pubmed: 37770790
doi: 10.1007/s10517-023-05905-z
pii: 10.1007/s10517-023-05905-z
doi:

Substances chimiques

Intercellular Signaling Peptides and Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

569-575

Informations de copyright

© 2023. Springer Science+Business Media, LLC, part of Springer Nature.

Références

Pittenger MF, Discher DE, Péault BM, Phinney DG, Hare JM, Caplan AI. Mesenchymal stem cell perspective: cell biology to clinical progress. NPJ Regen. Med. 2019;4:22. https://doi.org/10.1038/s41536-019-0083-6
doi: 10.1038/s41536-019-0083-6 pubmed: 31815001 pmcid: 6889290
Kehl D, Generali M, Mallone A, Heller M, Uldry AC, Cheng P, Gantenbein B, Hoerstrup SP, Weber B. Proteomic analysis of human mesenchymal stromal cell secretomes: a systematic comparison of the angiogenic potential. NPJ Regen. Med. 2019;4:8. https://doi.org/10.1038/s41536-019-0070-y
doi: 10.1038/s41536-019-0070-y pubmed: 31016031 pmcid: 6467904
Turinetto V, Vitale E, Giachino C. Senescence in human mesenchymal stem cells: functional changes and implications in stem cell-based therapy. Int. J. Mol. Sci. 2016;17(7):1164. https://doi.org/10.3390/ijms17071164
doi: 10.3390/ijms17071164 pubmed: 27447618 pmcid: 4964536
Lunyak VV, Amaro-Ortiz A, Gaur M. Mesenchymal stem cells secretory responses: senescence messaging secretome and immunomodulation perspective. Front. Genet. 2017;8:220. https://doi.org/10.3389/fgene.2017.00220
doi: 10.3389/fgene.2017.00220 pubmed: 29312442 pmcid: 5742268
Ratushnyy A, Ezdakova M, Buravkova L. Secretome of senescent adipose-derived mesenchymal stem cells negatively regulates angiogenesis. Int. J. Mol. Sci. 2020;21(5):1802. https://doi.org/10.3390/ijms21051802
doi: 10.3390/ijms21051802 pubmed: 32151085 pmcid: 7084202
Ratushnyy AY, Buravkova LB. Cell senescence and mesenchymal stromal cells. Hum. Physiol. 2020;46(1):85-93. https://doi.org/10.1134/S0362119720010132
doi: 10.1134/S0362119720010132
Ghosh D, Mejia Pena C, Quach N, Xuan B, Lee AH, Dawson MR. Senescent mesenchymal stem cells remodel extracellular matrix driving breast cancer cells to a more-invasive phenotype. J. Cell Sci. 2020;133(2):jcs232470. https://doi.org/10.1242/jcs.232470
Bertolo A, Baur M, Guerrero J, Pötzel T, Stoyanov J. Autofluorescence is a reliable in vitro marker of cellular senescence in human mesenchymal stromal cells. Sci. Rep. 2019;9(1):2074. https://doi.org/10.1038/s41598-019-38546-2
doi: 10.1038/s41598-019-38546-2 pubmed: 30765770 pmcid: 6376004
Hernandez-Segura A, Nehme J, Demaria M. Hallmarks of cellular senescence. Trends Cell Biol. 2018;28(6):436-453. https://doi.org/10.1016/j.tcb.2018.02.001
doi: 10.1016/j.tcb.2018.02.001 pubmed: 29477613
Frescas D, Roux CM, Aygun-Sunar S, Gleiberman AS, Krasnov P, Kurnasov OV, Strom E, Virtuoso LP, Wrobel M, Osterman AL, Antoch MP, Mett V, Chernova OB, Gudkov AV. Senescent cells expose and secrete an oxidized form of membrane-bound vimentin as revealed by a natural polyreactive antibody. Proc. Natl Acad. Sci. USA. 2017;114(9):E1668-E1677. https://doi.org/10.1073/pnas.1614661114
doi: 10.1073/pnas.1614661114 pubmed: 28193858 pmcid: 5338544
Campisi J. Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors. Cell. 2005;120(4):513-522. https://doi.org/10.1016/j.cell.2005.02.003
doi: 10.1016/j.cell.2005.02.003 pubmed: 15734683
Mavrogonatou E, Pratsinis H, Papadopoulou A, Karamanos NK, Kletsas D. Extracellular matrix alterations in senescent cells and their significance in tissue homeostasis. Matrix Biol. 2019;75-76:27-42. https://doi.org/10.1016/j.matbio.2017.10.004
doi: 10.1016/j.matbio.2017.10.004 pubmed: 29066153
Selman M, Pardo A. From pulmonary fibrosis to progressive pulmonary fibrosis: a lethal pathobiological jump. Am. J. Physiol. Lung Cell. Mol. Physiol. 2021;321(3):L600-L607. https://doi.org/10.1152/ajplung.00310.2021
Bauer AL, Jackson TL, Jiang Y. Topography of extracellular matrix mediates vascular morphogenesis and migration speeds in angiogenesis. PLoS Comput. Biol. 2009;5(7):e1000445. https://doi.org/10.1371/journal.pcbi.1000445
doi: 10.1371/journal.pcbi.1000445 pubmed: 19629173 pmcid: 2709079
Shibuya M. Vascular Endothelial Growth Factor (VEGF) and its receptor (VEGFR) signaling in angiogenesis: a crucial target for anti- and pro-angiogenic therapies. Genes Cancer. 2011;2(12):1097-1105. https://doi.org/10.1177/1947601911423031
doi: 10.1177/1947601911423031 pubmed: 22866201 pmcid: 3411125
Claesson-Welsh L, Welsh M. VEGFA and tumour angiogenesis. J. Intern. Med. 2013;273(2):114-127. https://doi.org/10.1111/joim.12019
doi: 10.1111/joim.12019 pubmed: 23216836
Liu L, Ratner BD, Sage EH, Jiang S. Endothelial cell migration on surface-density gradients of fibronectin, VEGF, or both proteins. Langmuir. 2007;23(22):11 168-11 173. https://doi.org/10.1021/la701435x
Claffey KP, Abrams K, Shih SC, Brown LF, Mullen A, Keough M. Fibroblast growth factor 2 activation of stromal cell vascular endothelial growth factor expression and angiogenesis. Lab. Invest. 2001;81(1):61-75. https://doi.org/10.1038/labinvest.3780212
doi: 10.1038/labinvest.3780212 pubmed: 11204275
Ponticos M. Connective tissue growth factor (CCN2) in blood vessels. Vascul. Pharmacol. 2013;58(3):189-193. https://doi.org/10.1016/j.vph.2013.01.004
doi: 10.1016/j.vph.2013.01.004 pubmed: 23380714
Ungvari Z, Valcarcel-Ares MN, Tarantini S, Yabluchanskiy A, Fülöp GA, Kiss T, Csiszar A. Connective tissue growth factor (CTGF) in age-related vascular pathologies. Geroscience. 2017;39(5-6):491-498. https://doi.org/10.1007/s11357-017-9995-5
doi: 10.1007/s11357-017-9995-5 pubmed: 28875415 pmcid: 5745206

Auteurs

D K Matveeva (DK)

Institute for Biomedical Problems, Russian Academy of Sciences, Moscow, Russia.

M I Ezdakova (MI)

Institute for Biomedical Problems, Russian Academy of Sciences, Moscow, Russia.

A Yu Ratushnyy (AY)

Institute for Biomedical Problems, Russian Academy of Sciences, Moscow, Russia. ratushkin@mail.ru.

Articles similaires

Killer Cells, Natural Animals Colorectal Neoplasms Decorin Adenoviridae

A dual role for PSIP1/LEDGF in T cell acute lymphoblastic leukemia.

Lisa Demoen, Filip Matthijssens, Lindy Reunes et al.
1.00
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Animals Mice Humans Cell Line, Tumor

High-throughput Bronchus-on-a-Chip system for modeling the human bronchus.

Akina Mori, Marjolein Vermeer, Lenie J van den Broek et al.
1.00
Humans Bronchi Lab-On-A-Chip Devices Epithelial Cells Goblet Cells

A key role for P2RX5 in brown adipocyte differentiation and energy homeostasis.

Maria Razzoli, Seth McGonigle, Bhavani Shankar Sahu et al.
1.00
Animals Adipocytes, Brown Mice Cell Differentiation Male

Classifications MeSH