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치근단질환에서 형질전환성장인자-β와 기질금속함유단백분해효소 발현에 관한 연구
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  • 치근단질환에서 형질전환성장인자-β와 기질금속함유단백분해효소 발현에 관한 연구
저자명
지정호,이수종,Chi. Jung-Ho,Lee. Su-Jong
간행물명
大韓齒科保存學會誌
권/호정보
1999년|24권 1호|pp.200-211 (12 pages)
발행정보
대한치과보존학회
파일정보
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The periapical response to injury is a complex interaction of inflammatory, immune, neural, vascular and synthetic activity. TGF-${eta}$ is a potent modulator of proliferation and differentiation in various tissue, seems to lead to an increase in extracellular matrix. MMP are a family of proteolytic enzyme that mediate the degradation of extracellular matric macromolecules, but little is known about theirs possible role in periapical tissue. The purpose of this study is to investigate the differential expression of TGF-${eta}$ and MMP-1 in tooth follicle, periapical abscess, granuloma and cyst. The expression of TGF-${eta}$ and MMP-1 in Periapical tissue was evaluated by immunohistochemical staining and Western blot analysis. Correlationship among the periapical lesions were stastically analyzed. The degree of MMP-1 expression in periapical abscess was higher than in any other periapical lesion, and stastically significant. TGF-${eta}$ expression is the prominent in granuloma than other periapical lesion, which was stastically significant. The increased expression of MMP and TGF-${eta}$ was not co-related with inflammatory cell infiltration degree of the periapical cyst. The expression degree of MMP and TGF-${eta}$ was not co-related with periapical abscess and cyst, but expression of MMP and TGF-${eta}$ showed strong positive co-relationship with periapical granuloma, which was stastically significant. TGF-${eta}$ expression by Western blot analysis was prominent in granuloma and cyst, and similar to the results by imunohistochemistry. MMP-1 expression is less than TGF-${eta}$, but there is not extreme difference between periapical lesion. These results suggest that TGF-${eta}$ and MMP may be involved in tissue remodeling and has an important role in progress or mediation of periapical lesions.