HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Moderate hypothermia induces protein SUMOylation in bone marrow stromal cells and enhances their tolerance to hypoxia.

Abstract
Acute cerebral infarction can progress rapidly, and there are limited specific and effective treatments. Small ubiquitin‑like modifiers (SUMOs) provide an important post‑translational modification of proteins. Following cerebral infarction, multiple proteins can combine with SUMOs to protect nerve cells. Furthermore, moderate hypothermia (core body temperature, 33‑34˚C) can increase the level of SUMOylation on multiple proteins. In the present study, it was examined whether moderate hypothermia increases the survival rate of bone marrow stromal stem cells (BMSCs) implanted in the cerebral ischemic penumbra via SUMOylation of multiple proteins. Firstly, BMSCs were exposed to oxygen‑glucose deprivation (OGD) under moderate hypothermic (33˚C) conditions. Subsequently, adult rats with middle cerebral artery occlusion were treated with a combination of BMSCs and moderate hypothermia (32‑34˚C). The results demonstrated that hypothermia promoted the combination of multiple proteins with SUMOs in BMSCs, and induced transport of SUMOs from the cytoplasm to the nucleus. Moderate hypothermia additionally reduced damage to BMSCs following OGD and improved BMSC survival following transplantation into the penumbra. These data suggest that moderate hypothermia may protect against BMSC injury via rapid SUMOylation of intracellular proteins. Thus, BMSC transplantation combined with moderate hypothermia may be a potential therapeutic strategy to treat cerebral infarction.
AuthorsWenbo Ren, Xiaofang Ma, Xiaozhi Liu, Yanxia Li, Zhongmin Jiang, Yujun Zhao, Chen Li, Xin Li
JournalMolecular medicine reports (Mol Med Rep) Vol. 16 Issue 5 Pg. 7006-7012 (Nov 2017) ISSN: 1791-3004 [Electronic] Greece
PMID28901483 (Publication Type: Journal Article)
Chemical References
  • RNA, Small Interfering
  • SUMO-1 Protein
  • SUMO2 protein, mouse
  • Small Ubiquitin-Related Modifier Proteins
  • Sumo3 protein, mouse
  • Ubiquitins
  • L-Lactate Dehydrogenase
  • Ubiquitin-Conjugating Enzymes
  • ubiquitin-conjugating enzyme UBC9
Topics
  • Animals
  • Apoptosis
  • Bone Marrow Cells (cytology)
  • Cell Hypoxia
  • Cells, Cultured
  • Disease Models, Animal
  • Hypothermia, Induced
  • Infarction, Middle Cerebral Artery (pathology)
  • L-Lactate Dehydrogenase (metabolism)
  • Male
  • RNA Interference
  • RNA, Small Interfering (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • SUMO-1 Protein (metabolism)
  • Small Ubiquitin-Related Modifier Proteins (metabolism)
  • Stromal Cells (cytology, metabolism)
  • Sumoylation
  • Ubiquitin-Conjugating Enzymes (antagonists & inhibitors, genetics, metabolism)
  • Ubiquitins (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: