Restoration of vascular endothelial integrity by mesenchymal stromal/stem cells in debilitating virus diseases

Hum Cell. 2022 Nov;35(6):1633-1639. doi: 10.1007/s13577-022-00785-3. Epub 2022 Sep 6.

Abstract

Endothelial dysfunction is one of the key cornerstone complications of emerging and re-emerging viruses which lead to vascular leakage and a high mortality rate. The mechanism that regulates the origin of endothelial dysregulation is not completely elucidated. Currently, there are no potential pharmacological treatments and curable management for such diseases. In this sense, mesenchymal stromal/stem cells (MSCs) has been emerging to be a promising therapeutic strategy in restoring endothelial barrier function in various lung disease, including ALI and ARDS. The mechanism of the role of MSCs in restoring endothelial integrity among single-strand RNA (ssRNA) viruses that target endothelial cells remains elusive. Thus, we have discussed the therapeutic role of MSCs in restoring vascular integrity by (i) inhibiting the metalloprotease activity thereby preventing the cleavage of tight junction proteins, which are essential for maintaining membrane integrity (ii) possessing antioxidant properties which neutralize the excessive ROS production due to virus infection and its associated hyper host immune response (iii) modulating micro RNAs that regulate the endothelial activation and its integrity by downregulating the inflammatory response during ssRNA infection.

Keywords: COVID-19; Cytotherapy; Endothelial damage; Stem cell; Viral haemorrhagic fever.

Publication types

  • Review

MeSH terms

  • Antioxidants / metabolism
  • Endothelial Cells / metabolism
  • Humans
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells* / physiology
  • Metalloproteases / metabolism
  • RNA
  • Reactive Oxygen Species / metabolism
  • Tight Junction Proteins / metabolism
  • Virus Diseases* / metabolism

Substances

  • Antioxidants
  • Reactive Oxygen Species
  • Tight Junction Proteins
  • RNA
  • Metalloproteases