TY - JOUR
T1 - Identification of tmem10/opalin as a novel marker for oligodendrocytes using gene expression profiling
AU - Kippert, Angelika
AU - Trajkovic, Katarina
AU - Fitzner, Dirk
AU - Opitz, Lennart
AU - Simons, Mikael
N1 - Funding Information:
We thank S. Bechtel and S. Wiemann (DKFZ, Heidelberg, Germany) for providing us with the ECFP-Tmem10 and Tmem10-EYFP plasmids and J. Trotter (University of Mainz, Germany) for antibodies. The work was supported by the Deutsche Forschungsgemeinschaft (SFB 523).
PY - 2008/4/25
Y1 - 2008/4/25
N2 - Background; During the development of the central nervous system, oligodendrocytes generate large amounts of myelin, a multilayered insulating membrane that ensheathes axons, thereby allowing the fast conduction of the action potential and maintaining axonal integrity. Differentiation of oligodendrocytes to myelin-forming cells requires the downregulation of RhoA GTPase activity. Results: To gain insights into the molecular mechanisms of oligodendrocyte differentiation, we performed microarray expression profiling of the oligodendroglial cell line, Oli-neu, treated with the Rho kinase (ROCK) inhibitor, Y-27632 or with conditioned neuronal medium. This resulted in the identification of the transmembrane protein 10 (Tmem10/Opalin), a novel type I transmembrane protein enriched in differentiating oligodendrocytes. In primary cultures, Tmem10 was abundantly expressed in O4-positive oligodendrocytes, but not in oligodendroglial precursor cells, astrocytes, microglia or neurons. In mature oligodendrocytes Tmem10 was enriched in the rims and processes of the cells and was only found to a lesser extent in the membrane sheets. Conclusion: Together, our results demonstrate that Tmem10 is a novel marker for in vitro generated oligodendrocytes.
AB - Background; During the development of the central nervous system, oligodendrocytes generate large amounts of myelin, a multilayered insulating membrane that ensheathes axons, thereby allowing the fast conduction of the action potential and maintaining axonal integrity. Differentiation of oligodendrocytes to myelin-forming cells requires the downregulation of RhoA GTPase activity. Results: To gain insights into the molecular mechanisms of oligodendrocyte differentiation, we performed microarray expression profiling of the oligodendroglial cell line, Oli-neu, treated with the Rho kinase (ROCK) inhibitor, Y-27632 or with conditioned neuronal medium. This resulted in the identification of the transmembrane protein 10 (Tmem10/Opalin), a novel type I transmembrane protein enriched in differentiating oligodendrocytes. In primary cultures, Tmem10 was abundantly expressed in O4-positive oligodendrocytes, but not in oligodendroglial precursor cells, astrocytes, microglia or neurons. In mature oligodendrocytes Tmem10 was enriched in the rims and processes of the cells and was only found to a lesser extent in the membrane sheets. Conclusion: Together, our results demonstrate that Tmem10 is a novel marker for in vitro generated oligodendrocytes.
UR - http://www.scopus.com/inward/record.url?scp=44449106013&partnerID=8YFLogxK
U2 - 10.1186/1471-2202-9-40
DO - 10.1186/1471-2202-9-40
M3 - Article
C2 - 18439243
AN - SCOPUS:44449106013
SN - 1471-2202
VL - 9
JO - BMC Neuroscience
JF - BMC Neuroscience
M1 - 40
ER -