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¾ç¼¼¶õ, Á¶¼º´ë, ¾È³²½Ä, Á¤Áö¿ø, ¹ÚÁؼ®, Tiep Nguyen Ba, ¹Ú±â¼ö, È«Àμ±, Á¶ÀºÇý, ¼­¹Î¼ö, Yoon Byong-Su, ÀÌ¿ë¼ø, °­°æ¼±,
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¾ç¼¼¶õ ( Yang Se-Ran ) 
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Á¶¼º´ë ( Cho Sung-Dae ) 
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¾È³²½Ä ( Ahn Nam-Shik ) 
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Á¤Áö¿ø ( Jung Ji-Won ) 
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¹ÚÁؼ® ( Park Joon-Suk ) 
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 ( Tiep Nguyen Ba ) 
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¹Ú±â¼ö ( Park Ki-Su ) 
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È«Àμ± ( Hong In-Sun ) 
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Á¶ÀºÇý ( Jo Eun-Hye ) 
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¼­¹Î¼ö ( Seo Min-Su ) 
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 ( Yoon Byong-Su ) 
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ÀÌ¿ë¼ø ( Lee Yong-Soon ) 
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°­°æ¼± ( Kang Kyung-Sun ) 
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Abstract


Gap junctional intercellular communication (GJIC) plays a key role during development, process of tissue differentiation, and in maintenance of adult tissue homeostasis. Neural stem cells leading to formation of cell clusters termed "neurospheres", can differentiate into neurons, oligodendrocytes, and astrocytes. We investigated the expression levels and distribution of connexin43 (Cx43) and connexin32 (Cx32), abundant gap junctional protein in neural cells and in neurospheres isolated from rat fetus embryonic day (ED) 17. During differentiation of neurospheres, expression of Cx43 and 32 were increased time-dependently within 72 h, and then decreased at 7 day in western blot analysis. TPA-induced inhibition of GJIC was confirmed by decreased fluorescence by SL/DT assay, and induced hyperphosphorylation of Cx43 while no changes in Cx32 levels in western blot assay. Our results indicate that GJIC may be a crucial role in the differentiation of neuronal stem cell. And this GJIC can be inhibited by TPA through the hyperphosphorylation of Cx43.

Å°¿öµå

Neurosphere;Stem cells;Gap junction;Cx43;Cx32;Differentiation

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