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CHANGES OF CYCLINS, CYCLIN DEPENDENT KINASES, CYCLIN DEPENDENT KINASE INHIBITORS DURING GLOSSAL DEVELOPMENT IN THE RATS

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Abstract

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1. ØØãÕ 1ìí ý­ÀÇ ÍéâÐá¬øàÀÇ Ý¾ó·á¬øà⦴ ÓßðÎÏØ¿¡ ÝïÇÏ¿© ¸ðµç à÷íþì×í­¿¡¼­ êóëòàõ
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3. ØØãÕ 3ìíÀÇ ÍéâÐá¬øàÀÇ Ý¾ó·û¡÷¾´Â IGF-I¿Í PDGF°¡ ÓóøÖµÈ ØØãÕô÷ÀÇ øúØüÀÌ °¡Àå ³Ð
°í ³³ÀÛÇÏ°Ô Ý¾ó·µÈ ÍéâÐá¬øàµéÀÌ Îºó̵ǾúÀ¸³ª, EGF´Â ñéÔõÓø, TGF-¥â´Â ÓßðÎÏØ°ú ÇÔ²²
Ú°å°ÇÑ á¬øàݾó·û¡÷¾¸¦ ³ªÅ¸³»¾ú´Ù.
4. ØØãÕ 7ìí ý­ÀÇ Íéû¡à÷ Óø´Â ÓßðÎÏØ¿¡ ÝïÇØ ãùúÐÏØ¿¡¼­ úéîÊÇÏ¿´À¸¸ç, PDGF¿Í TGF-
¥â ÷áæ¨ÏØ¿¡¼­ èÚàüÇÑ Íéà÷íþÀ» º¸¿´À¸¸ç, IGF-I ÓóøÖÏØ¿¡¼­´Â ãæßæÍéÀÌ ¾çÂÊ ÍéÓ®Âʺ¸´Ù´Â
Äݶó°ÕÂÊÀ¸·Î ö°Øü¿¡¼­ à÷íþµÈ °ÍÀÌ Îºó̵Ǿú°í, EGF¿¡¼­´Â ãæßæÍéÀÌ °ÅÀÇ Îºó̵ÇÁö ¾Ê¾Ò
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äÌïÒàõ¿¡ Ðöæ¨ÇÏ¿© ÍéðÚòÄÀÇ ì¹ãÕ ¹× ÞÖÖùµÇ³ª ¾ÕÀ¸·Îµµ ´õ ¸¹Àº æÚϼ¿Í κóÌÀÌ ù±é©ÇÒ °Í
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The molecular mechanisms that regulate glossal muscle cell cycle and terminal
differentiation remain largely unknown. To determine which cyclins, cyclin dependent
kinases (CDKs), cyclin dependent kinase inhibitors (CKIs) are important for glossal cell
proliferation, we have examined expression of cyclins CDKs, CKIs during normal glossal
muscle development in the rat.
All cyclins, CDKs, and KIP/CIP family of CKIs were highly expressed during fetal
glossal muscle development, then they decreased at different rates after birth. While the
mRNAs of cyclin Dl, D3, E , A, and B decreased gradually in glossal muscle during all
stages of development, the protein levels of these cyclins decreased differently in tongue
during pre- and postnatal development. While the functionally active formed of cyclin
Dl, cyclin D3 and E proteins were observed until 7 days after birth, cyclin A and B
proteins were decreased more slowly. While the CDK4, CDK6, CDK2, cdc2, and
proliferating cell nuclear antigen (PCNA) proteins were higllly present during fetal
glossal muscle development and gradually decreased during postnatal development.
Particularly, cdc2 levels decreased markedly after birth. Immunohistochemical data for
PCNA was consistent with Western blotting data for PCNA temporally and spatially.
The mRNA and protein levels of p21, p27, and p57 were high, then their levels changed
differently during glossal development. While the mRNA levels of p21 and p57 decreased
gradually, the mRNA level of p27 did not change during glossal development. While the
protein levels of p21 and p57 in tongue decreased markedly after birth, the protein levels
of p27 increased slightly after birth, then decreased at adulthood.
These findings suggest that the all cyclins and CDKs observed are involved in glossal
muscle cell cycle, and reduction of cyclins and CDKs and induction of p21 are
associated with the withdrawal of glossal muscle cell cycle after birth.

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