Back to Search Start Over

Effects of Hydrogen Sulfide Donor NaHS on Porcine Vascular Wall-Mesenchymal Stem Cells

Authors :
Augusta Zannoni
Debora La Mantia
Roberta Salaroli
Chiara Bernardini
Cristina Algieri
Monica Forni
Alessandra Pagliarani
Salvatore Nesci
Bernardini C.
La Mantia D.
Nesci S.
Salaroli R.
Algieri C.
Pagliarani A.
Zannoni A.
Forni M.
Source :
International Journal of Molecular Sciences, Volume 21, Issue 15, International Journal of Molecular Sciences, Vol 21, Iss 5267, p 5267 (2020)
Publication Year :
2020
Publisher :
MDPI, 2020.

Abstract

Hydrogen sulfide (H2S) is now considered not only for its toxicity, but also as an endogenously produced gas transmitter with multiple physiological roles, also in maintaining and regulating stem cell physiology. In the present work, we evaluated the effect of a common H2S donor, NaHS, on porcine vascular wall&ndash<br />mesenchymal stem cells (pVW&ndash<br />MSCs). pVW&ndash<br />MSCs were treated for 24 h with increasing doses of NaHS, and the cell viability, cell cycle, and reactive oxygen species (ROS) production were evaluated. Moreover, the long-term effects of NaHS administration on the noteworthy characteristics of pVW&ndash<br />MSCs were analyzed. The MTT test revealed no alteration in cell viability, however, the cell cycle analysis demonstrated that the highest NaHS dose tested (300 &mu<br />M) determined a block in S phase, which did not depend on the ROS production. Moreover, NaHS (10 &mu<br />M), continuously administered in culture for 21 days, was able to significantly reduce NG2, Nestin and PDGFR-&beta<br />expression. The pro-angiogenic attitude of pVW&ndash<br />MSCs was partially reduced by NaHS: the cells maintained the ability to grow in spheroid and sprouting from that, but endothelial markers (Factor VIII and CD31) were reduced. In conclusion, NaHS can be toxic for pVW&ndash<br />MSCs in high doses, while in low doses, it influences cellular physiology, by affecting the gene expression with a slowing down of the endothelial lineage.

Details

Language :
English
ISSN :
14220067
Volume :
21
Issue :
15
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....87854dc30f054669002591e15a3fd539