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Stathmin-like 2, a developmentally-associated neuronal marker, is expressed and modulated during osteogenesis of human mesenchymal stem cells.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2008 Sep 12; Vol. 374 (1), pp. 64-8. Date of Electronic Publication: 2008 Jul 09. - Publication Year :
- 2008
-
Abstract
- Stathmin-like 2 (STMN2) protein, a neuronal protein of the stathmin family, has been implicated in the microtubule regulatory network as a crucial element of cytoskeletal regulation. Herein, we describe that STMN2 expression increases at both mRNA and protein levels during osteogenesis of human mesenchymal stem cells derived from adipose tissue (hMADS cells) and bone marrow (hBMS cells), whereas it decreases to undetectable levels during adipogenesis. STMN2 protein is localized in both Golgi and cytosolic compartments. Its expression appears modulated in osteoblasts by nerve growth factor, dexamethasone or RhoA kinase inhibitor Y-27632 which are known effectors of osteogenesis. Thus STMN2 appears a novel marker of osteogenesis and osteoblast per se, that could play a role in the regulation of the adipocyte/osteoblast balance.
- Subjects :
- Adipocytes metabolism
Adipogenesis
Adipose Tissue metabolism
Amides pharmacology
Biomarkers metabolism
Bone Marrow Cells cytology
Bone Marrow Cells metabolism
Cytosol metabolism
Dexamethasone pharmacology
Golgi Apparatus metabolism
Humans
Membrane Proteins genetics
Mesenchymal Stem Cells cytology
Neurons metabolism
Osteoblasts drug effects
Osteoblasts metabolism
Protein Kinase Inhibitors pharmacology
Pyridines pharmacology
RNA, Messenger biosynthesis
RNA, Messenger genetics
Stathmin
rho-Associated Kinases antagonists & inhibitors
Membrane Proteins biosynthesis
Mesenchymal Stem Cells metabolism
Osteogenesis
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 374
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 18611392
- Full Text :
- https://doi.org/10.1016/j.bbrc.2008.06.121