Inhibition of mouse GPM6A expression leads to decreased differentiation of neurons derived from mouse embryonic stem cells

• Published in: Stem cells and development Vol. 17; no. 4; p. 641
• Main Authors: Michibata, Hideo, Okuno, Tsuyoshi, Konishi, Nae, Wakimoto, Koji, Kyono, Kiyoshi, Aoki, Kan, Kondo, Yasushi, Takata, Kazuyuki, Kitamura, Yoshihisa, Taniguchi, Takashi
• Format: Journal Article
• Language: English
• Published: United States 01.08.2008
• Subjects: Animals; Antigens, Differentiation - biosynthesis; Antigens, Differentiation - genetics; Cell Differentiation - physiology; Central Nervous System - cytology; Central Nervous System - metabolism; Cercopithecus aethiops; COS Cells; Embryonic Stem Cells - cytology; Embryonic Stem Cells - metabolism; Gene Expression; Gene Expression Regulation - physiology; Membrane Glycoproteins - biosynthesis; Membrane Glycoproteins - genetics; Mice; Nerve Tissue Proteins - biosynthesis; Nerve Tissue Proteins - genetics; Neurons - cytology; Neurons - metabolism; Promoter Regions, Genetic - genetics; RNA, Small Nuclear - genetics
• ISSN: 1557-8534
• DOI: 10.1089/scd.2008.0088

Glycoprotein M6A (GPM6A) is known as a transmembrane protein and an abundant cell surface protein on neurons in the central nervous system (CNS). However, the function of GPM6A is still unknown in the differentiation of neurons derived from embryonic stem (ES) cells. To investigate the function of GPM6A, we generated knockdown mouse ES cell lines (D3m-shM6A) using a short hairpin RNA (shRNA) expression vector driven by the U6 small nuclear RNA promoter, which can significantly suppress the expression of mouse GPM6A mRNA. Real-time polymerase chain reaction (real-time PCR) and immunocytochemical analysis showed that expression of shRNA against GPM6A markedly reduced the expression of neuroectodermal-associated genes (OTX1, Lmx1b, En1, Pax2, Pax5, Sox1, Sox2, and Wnt1), and also the number of neural stem cells (NSC) derived from D3mshM6A cells compared to control vector-transfected mouse ES cells (D3m-Mock). Moreover, our results show a decrease in both the number of neuronal markers and the number of differentiating neuronal cells (cholinergic, catecholaminergic, and GABAergic neurons) from NSC in D3m-shM6A cells. Hence, our findings suggest that expression level of GPM6A is directly or indirectly associated with the differentiation of neurons derived from undifferentiated ES cells.