Journal of the Korean Ophthalmological Society 2006;47(7):1110-1116.
Published online July 31, 2006.
The Regulation of MMP-2 and -14 Expressions by TGF-beta in Lens Epithelial Cells.
Min Jung Son, Jong Tak Kim, Choun Ki Joo
Laboratory of Ophthalmology and Visual Science, Catholic Research Institutes of Medical Science, Catholic University Medical College, Seoul, Korea. ckjoo@catholic.ac.kr
수정체 상피세포에서 TGF-β에 의한 MMP-2와 MMP-14의 발현과 조절 기전
손민정,김종탁,주천기
Laboratory of Ophthalmology and Visual Science, Catholic Research Institutes of Medical Science, Catholic University Medical College, Seoul, Korea
Correspondence:  Jong Tak Kim, Ph.D.
Abstract
PURPOSE
TGF-beta is a key regulator of epithelial-mesenchymal transition. Among the TGF-beta responses, cell migration is closely associated with the expression of matrix metalloproteinases (MMPs). Therefore, we determined which MMPs are regulated by TGF-beta and examined the TGF-beta signaling involved in this event, focusing on Src family tyrosine kinases (SFKs) METHODS: First we examined the expression of MMPs in rat lens explant culture treated with TGF-beta and LECs attached to the anterior capsules of patients with nuclear (N), anterior polar (AP) cataracts using RT-PCR and immunofluorescence staining. It was examined whether the expression of MMPs is regulated by SFKs. RESULTS: The study using RT-PCR and immunofluorescence staining showed the expression of MMP-2 and -14 in explants and the expression of MMP-14 LECs of AP cataracts. The expression of MMP-2 and -14 was blocked by PP2 in explants. Furthermore, the activated form of SFKs was observed in LECs of AP cataracts by immunofluorescence staining. CONCLUSIONS: We suggest a novel role of SFKs signaling in the expression of MMP-14 induced by TGF-beta.
Key Words: Lens epithelial cell;Matrix metalloproteinase;Nuclear and anterior polar cataract;Transforming growth factor-beta


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