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IpriflavoneÀÌ °ñ ¼¼Æ÷ÁÖ(MC3T3-El cell line)ÀÇ CollagenÇÕ¼º¿¡ ¹ÌÄ¡´Â ¿µÇâ

EFFECTS OF IPRIFLAVONE ON COLLAGEN SYNTHESIS OF OSTEOBLAST-LIKE CELLS(MC3T3-El CELL LINE)

¼Ò¼Ó »ó¼¼Á¤º¸
¾çÀ±¼®/Yun-Seok Yang

Abstract

Ipriflavone(IP)Àº °ñÈí¼ö ¾ïÁ¦È¿°ú¿Í °ñÇü¼º ÃËÁøÈ¿°ú¸¦ Áö´Ï´Â ¾à¹°·Î º¸°íµÇ¾î ¿Ô´Ù.
ÀÌ·¯ÇÑ IPÀÇ Æ¯¼º ¶§¹®¿¡ °ñÀÇ Ä¡À¯¸¦ ÃËÁø½ÃÅ°±â À§ÇÑ ¾à¹°·Î¼­ ±¸°­¿Ü°ú ¿µ¿ª¿¡¼­ ¾²ÀÏ
¼öµµ ÀÖÀ¸¸®¶ó »ý°¢µÇ¾ú´Ù.
ÀÌ¿¡ ÀúÀÚ´Â ±× µ¿¾È º¸°íµÇ¾î¿Â IPÀÇ °ñ Çü¼º ÃËÁøÈ¿°ú°¡ ½ÇÁ¦·Î ³ªÅ¸³ª´ÂÁö¸¦ È®ÀÎÇÏ°í
¶ÇÇÑ ¾î¶² ³óµµ¿¡¼­ ³ªÅ¸³ª´ÂÁö¸¦ ¾Ë¾Æº¸±â À§ÇØ IP¸¦ ¼­·Î ´Ù¸¥ ³óµµ·Î ÇÏ¿© °ñ¼¼Æ÷ÁÖ
(MC3T3-El cell line)ÀÇ ¹èÁö¿¡ ³ÖÀº ÈÄ, °ñ Çü¼ºÀÇ ÁöÇ¥·Î ¾²ÀÏ ¼ö ÀÖ´Â collagenÇÕ¼ºÁ¤µµ
¸¦ º¸°íÀÚ ÇÏ¿´À¸¸ç ÀÌ ÀڷḦ ¾ÕÀ¸·ÎÀÇ in vivo µ¿¹°½ÇÇè ¿¬±¸ÀÇ ±âÃÊÀÚ·á·Î »ç¿ëÄÚÀÚ ÇÏ
¿´´Ù.
º» ¿¬±¸¿¡¼­ IPÀÇ °ñÇü¼º ÃËÁøÈ¿°ú¸¦ collagen ÇÕ¼ºÁ¤µµÀÇ ÃøÁ¤À» ÅëÇØ È®ÀÎÇÏ¿´°í, ƯÈ÷
IPÀÌ 10-7M³óµµÀÏ ¶§ ÇöÀúÇÑ collagenÇÕ¼ºÀÇ Áõ°¡¸¦ °üÂûÇÏ¿´À¸¸ç ¾ÕÀ¸·ÎÀÇ
µ¿¹°½ÇÇèµîÀ» ÅëÇØ ±¸°­¿Ü°ú ¿µ¿ª¿¡¼­ÀÇ »ç¿ë°¡´É¼º¿¡ ´ëÇØ Á»´õ ¿¬±¸ÇØ º¸°íÀÚ ÇÑ´Ù.
#ÃÊ·Ï#
Collagen, the most abundant protein in connective tissue, represents 90% of the
organic matrix of bone.
The collagen synthesis has been known as a good marker for the bone formation.
Therefore, 1 used the degree of collagen synthesis as a marker for the interpretation of
the effects of Ipriflavone(If) on the osteoblast-like cells.
In this study, 1 observed that IP stimulate the collagen systhesis of osteoblast-like
cells. This confirms previous in vitro observations on If's stimulation of collagen
systhesis by human otosclerotic auditory ossicel samples. This study showed that the
concentration which stimulate the collagen synthesis of osteoblast-like cells was 10-7M.
We also observed that the higher concentration (10-6M,10-5 M) inhibited the collagen
synthesis of osteoblast-like cells.
These date are not coincident with previous study(Sziklai et at . 1985) which showed
that the concentration of IP which stimulated the osteoblasts-like cells was 10-sM, but
coincident with the study(Ribari et at'1987) in the that 10-sM reduced the collagenous
protein synthesis.
These differences may be due to differences in culture conditions, cell species, and
durration of the exposure of the cells to IP.
PGE2 that is secreted by osteoblasts is currently the effective stimulator
of bone resorption and enhances the resorptive activity of osteoclasts. It also play a role
in collagen synthesis and high concentrations and increase.
Ribari et al reported that IP 10-5M decreased the collagen synthesis but
increased collagen synthesis inhibited by low concentration of PGE2.
Therefore, I think that the different concentration of PGE2 which was
secreted by osteoblast-like cells may be also a reason for the different results.
In conclusion, this study suggests that IP stimulated collagen synthesis of
osteoblast-like cells in 10-7M concentration.
Furthermore, IP may be used as a agent that facilitate bone healing in oral
maxillofacial surgery.

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