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FGF signalingÀÌ ¿¬°ñ Çü¼º¿¡ ¹ÌÄ¡´Â ¿µÇâ

THE EFFECT OF FIBROBLAST GROWTH FACTOR SIGNALING ON CARTILAGE FORMATION

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Abstract

¸·³»°ñÈ­¿Í ¿¬°ñ³»°ñÈ­ µîÀÇ Á¤»óÀûÀÎ °ñ°Ý ¼ºÀåÀº ¼¶À¯¾Æ¼¼Æ÷ ¼ºÀåÀÎÀÚ (FGF)¿Í ÀÌµé ¼ö¿ëüµé(FGFR)¿¡ ÀÇÇÑ ½ÅÈ£Àü´Þü°è¿¡ ÀÇÇØ Á¶ÀýµÈ´Ù. ¶ÇÇÑ Àü»çÁ¶ÀýÀÎÀÚÀÎ Runx2(Cbfa1/Pebp2¥áA/AML3)´Â °ñ¾Æ¼¼Æ÷ºÐÈ­ »Ó¸¸ ¾Æ´Ï¶ó °ñÇü¼º¿¡µµ ÇʼöÀûÀÎ À¯ÀüÀÚ·Î ¾Ë·ÁÁ® ÀÖ´Ù. FGF signalingÀÌ mouseÀÇ µÎ°³°ü°ú ÇϾǿ¡¼­ÀÇ ¿¬°ñ Çü¼º¿¡ ¾î¶² ¿µÇâÀ» ¹ÌÄ¡°í ÀÖÀ¸¸ç, ÀÌ °úÁ¤¿¡¼­ Runx2ÀÇ ¿¬°ü¼ºÀ» ¾Ë¾Æº¸°íÀÚ in vivo ¹× in vitro ½ÇÇèÀ» ½ÃÇàÇÏ¿© ´ÙÀ½°ú °°Àº °á°ú¸¦ ¾ò¾ú´Ù.
µÎ°³°ü°ú ÇϾÇÀ» Alcian blue ¿°»öÇÑ °á°ú ½Ã»óµÎ°³ºÀÇպΠ¿¬°ñÀº Å»ý16ÀϺÎÅÍ, Meckel¢¥s ¿¬°ñÀº Å»ý11ÀϺÎÅÍ Çü¼ºµÇ±â ½ÃÀÛÇÏ¿´´Ù. ÀÌµé ¿¬°ñ¼¼Æ÷µéÀÇ ¼º»óÀ» ¾Ë¾Æº¸±âÀ§ÇÑ in situ hybridization °á°ú ½Ã»óµÎ°³ºÀÇպΠ¿¬°ñ ¹× Meckel¢¥s ¿¬°ñ ¸ðµÎ¿¡¼­ type ¥± collagenÀº ¹ßÇöµÇ¾úÀ¸³ª, Type ¥¹ collagenÀº ¹ßÇöµÇÁö ¾Ê¾Ò´Ù. Runx2 mRNA´Â ½Ã»óµÎ°³ºÀÇպΠ¿¬°ñ°ú Meckel¢¥s ¿¬°ñ ¸ðµÎ¿¡¼­ ¹ßÇöµÇÁö ¾Ê¾ÒÁö¸¸, ÀÌµé ¿¬°ñµéÀÇ °¡ÀåÀÚ¸®¸¦ µÑ·¯½Î°í ÀÖ´Â µ¶Æ¯ÇÑ ¹ßÇö¾ç»óÀ» ³ªÅ¸³»¾ú´Ù. µÎ°³ºÀÇպο¡¼­ÀÇ FGF2 proteinÀÇ ±¹¼ÒÀû Àû¿ëÀº µÎ°³ºÀÇպΠÇϹæÀÇ ¿¬°ñÇü¼ºÀ» ¾ïÁ¦ÇÏ¿´´Ù. ¶ÇÇÑ ÇϾÇÀÇ Meckel¢¥s ¿¬°ñ ¹ß»ý ºÎÀ§¿¡ FGF2 proteinÀÇ ±¹¼ÒÀû Àû¿ë ¿ª½Ã Meckel¢¥s ¿¬°ñÀÇ Çü¼ºÀ» ¾ïÁ¦ÇÏ¿´´Ù. FGF2 proteinÀº ½Ã»óµÎ°³ºÀÇպλóÀÇ bead ÁÖÀ§·Î Runx2ÀÇ ¹ßÇöÀ» À¯µµÇÏ¿´´Ù.
ÀÌ °á°úµéÀ» Á¾ÇÕÇغ¼ ¶§, FGF signalingÀº °ñ¾Æ¼¼Æ÷¿Í ¿¬°ñ¾Æ¼¼Æ÷°¡ °øÁ¸ÇÏ°í ÀÖ´Â Á¶Á÷¿¡¼­ÀÇ ¿¬°ñ Çü¼ºÀ» ¾ïÁ¦ÇÏ°í ÀÖÀ½À» ½Ã»çÇØ ÁÖ°í ÀÖÀ¸¸ç, ÀÌ °úÁ¤¿¡¼­ FGF signalingÀº ºÎºÐÀûÀ¸·Î Runx2À¯ÀüÀÚÀÇ ¹ßÇöÀ» Á¶ÀýÇÏ¹Ç·Î½á ¿¬°ñ¼¼Æ÷ÀÇ Áõ½Ä°ú ºÐÈ­¿¡ °ü¿©ÇÒ °ÍÀ¸·Î »ç·áµÈ´Ù.
Fibroblast growth factor (FGF) / FGF receptor (FGFR) mediated signaling is required for skeletogenesis in¡þcluding intramembranous and endochondral ossifications. Runx2 ((¢¥,bfa1/Pebp2aA/AML3) is an essential tran¡þscription factor for osteoblast differentiation and bone formation. Murine calvaria and mandible are concurrently undergoing both intramembranous bone and cartilage formations in the early developmental stage. However the mechanism by which these cartilage formations are regulated remains unclear. To elucidate the effect of FGF signaling on development of cranial sutural catilage and Meckel s cartilage and to understand the role of Runx2 in these processs. we have done both in vivo and in vitro experiments. Alcian blue staining showed that cartilage formation in sagittal suture begins from embryonic stage 16 (E16). Meckel¢¥s cartilage formation in mandible from E12. We analyzed by in situ hybridization the characteristics of cartilage cells that type lI collagen, not type X collagen. was expressed in sagittal sutural cartilage and Meckel¢¥ s cartilage. In addition, Runx2 was not expressed in Meckel s cartialge as well as sagittal sutural cartilage, except specific expression pattern
only surrounding both cartilages. FGF signaling pathway was further examined in vitro. Beads soaked in FGF2 placed on the sagittal suture and mandible inhibited both sutural and Meckel¢¥ s cartilage formations. We next examined whether Runx2 gene lies in FGF siganling pathway during regulation of catilage formation. Beads soaked in FGF2 on sagittal suture induced Runx2 gene expression.
These results suggest that FGF signaling inhibits formations of sagittal sutural and Meckel s cartilages, also propose that FGF siganling is involved in the proliferation and differentiation of chondroblasts through regulat¡þing the transcription factor Runx2.

Å°¿öµå

FGF signaling;Runx2;µÎ°³ºÀÇÕºÎ;Meckel¢¥s ¿¬°ñ;¿¬°ñÇü¼º;FGF signaling;Runx2;Cranial suture;Meckel¢¥s cartilage;Chondrogenesis

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