Thursday, September 10, 2009

9/11 pubmed: adipose stem cell

Please add updates@feedmyinbox.com to your address book to make sure you receive these messages in the future.
pubmed: adipose stem cell Feed My Inbox

THE ORIGIN OF INTERMUSCULAR ADIPOSE TISSUE AND ITS PATHOPHYSIOLOGICAL IMPLICATIONS.
September 10, 2009 at 7:55 am

THE ORIGIN OF INTERMUSCULAR ADIPOSE TISSUE AND ITS PATHOPHYSIOLOGICAL IMPLICATIONS.

Am J Physiol Endocrinol Metab. 2009 Sep 8;

Authors: Vettor R, Milan G, Franzin C, Sanna M, De Coppi P, Rizzuto R, Federspil G

The intermuscular adipose tissue (IMAT) is a depot of adipocytes located between muscle bundles. Several investigations have been recently carried out to define the phenotype, the functional characteristics and the origin of the adipocytes present in this depot. Among the different mechanisms that could be responsible for the accumulation of fat in this site the dysdifferentiation of muscle-derived stem cells or other mesenchymal progenitors has been postulated, turning them into cells with an adipocyte phenotype. In particular, muscle satellite cells (SCs), a heterogeneous stem cell population characterized by plasticity and self-renewal that allow muscular growth and regeneration, can acquire features of adipocytes including the abilities to express adipocyte specific genes and accumulate lipids. Failure to express the transcription factors that direct mesenchymal precursors into fully differentiated functionally specialized cells may be responsible for their phenotypic switch into the adipogenic lineage. We proved that also human SCs possess a clear adipogenic potential that could explain the presence of mature adipocytes within skeletal muscle. This occurs under some pathological conditions (i.e., primary myodystrophies, obesity, hyperglycaemia, high plasma free fatty acids, hypoxia, etc) or as a consequence of thiazolidinedione treatment or simply because of a sedentary lifestyle or during aging. Several pathways and factors (PPARs, WNT growth factors, Myokines, GEF-GAP-Rho, p66shc, mitochondrial ROS production, PKCbeta) could be implicated in the adipogenic conversion of SCs. The understanding of the molecular pathways that regulates muscle-to-fat conversion and SC behaviour could explain the increase in IMAT depots that characterize many metabolic diseases and age-related sarcopenia. Key words: intermuscular adipose tissue, muscle satellite cells, mesenchymal stem cells, myogenesis, adipogenesis.

PMID: 19738037 [PubMed - as supplied by publisher]

 

This email was sent to agupta1213+termsc@gmail.comManage Your Account
Don't want to receive this feed any longer? Unsubscribe here.

No comments: