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Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cells.

Abstract
Tuftelin, an acidic protein, thought to play a role in the initial stages of ectodermal enamel mineralization, has since been detected in mesenchymal-derived tissues. During bone/cartilage development and regeneration, mesenchymal stem cells (MSCs) undergo an avascular period in a hypoxic environment, involving induction of hypoxia-inducible factor 1-alpha (HIF-1-alpha), a key component in this process. In the present study we investigated, in a mouse mesenchymal C3H10T1/2 stem cell model, the hypothesis that oxygen stress modulates tuftelin 1 expression in relation to HIF-1-alpha (Hif1a), in a mouse mesenchymal C3H10T1/2 stem cell model. The results of the present study showed a biphasic induction of tuftelin, similar to the pattern of HIF-1-alpha expression, in MSCs subjected to a hypoxic insult of 1% O(2) through a period of 2-24 h. Immunocytochemistry analysis of the cells exposed to hypoxic insult for 2-24 h revealed the same biphasic pattern of tuftelin protein expression. Tuftelin localization appears to be mainly in the cytoplasm, and concentrated at the perinuclear region of the cells by 24 h of hypoxic insult. Based on our previous studies using the neuronal PC12 cell model, in which tuftelin induction was mediated by Hif1a, we propose that tuftelin is a member of oxygen-sensitive genes and implicated in the adaptive mechanisms regulating MSC function.
AuthorsDan Deutsch, Nechama Silverstein, Dekel Shilo, Shimon Lecht, Philip Lazarovici, Anat Blumenfeld
JournalEuropean journal of oral sciences (Eur J Oral Sci) Vol. 119 Suppl 1 Pg. 55-61 (Dec 2011) ISSN: 1600-0722 [Electronic] England
PMID22243227 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2011 Eur J Oral Sci.
Chemical References
  • Dental Enamel Proteins
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • tuftelin
  • L-Lactate Dehydrogenase
Topics
  • Adaptation, Physiological
  • Animals
  • Cell Death
  • Cell Hypoxia (physiology)
  • Cells, Cultured
  • Dental Enamel Proteins (biosynthesis, genetics)
  • Gene Expression Regulation, Developmental
  • Hypoxia-Inducible Factor 1, alpha Subunit (biosynthesis, genetics)
  • L-Lactate Dehydrogenase (metabolism)
  • Mesenchymal Stem Cells (metabolism)
  • Mice
  • Mice, Inbred C3H

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