Effects of cathepsin K deficiency on intercellular junction proteins, luminal mucus layers, and extracellular matrix constituents in the mouse colon

被引:12
作者
Arampatzidou, Maria [1 ]
Schuette, Andre [2 ]
Hansson, Gunnar C. [2 ]
Saftig, Paul [3 ]
Brix, Klaudia [1 ]
机构
[1] Jacobs Univ Bremen, Sch Sci & Engn, Res Ctr MOLIFE Mol Life Sci, D-28759 Bremen, Germany
[2] Univ Gothenburg, Dept Med Biochem, S-41390 Gothenburg, Sweden
[3] Univ Kiel, Inst Biochem, D-24118 Kiel, Germany
基金
瑞典研究理事会;
关键词
cysteine cathepsins; colon; intercellular junctions; intestinal barrier; mucus; INFLAMMATORY-BOWEL-DISEASE; CYSTEINE CATHEPSINS; EPITHELIAL-CELLS; E-CADHERIN; EXPRESSION; MUCIN; ROLES; OVEREXPRESSION; LOCALIZATION; ORGANIZATION;
D O I
10.1515/hsz-2012-0204
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cathepsin K has been shown to exhibit antimicrobial and anti-inflammatory activities in the mouse colon. To further elucidate its role, we used Ctsk(-/-) mice and demonstrated that the absence of cathepsin K was accompanied by elevated protein levels of related cysteine cathepsins (cathepsins B, L, and X) in the colon. In principle, such changes could result in altered subcellular localization; however, the trafficking of cysteine cathepsins was not affected in the colon of Ctsk(-/-) mice. However, cathepsin K deficiency affected the extracellular matrix constituents, as higher amounts of collagen IV and laminin were observed. Moreover, the localization pattern of the intercellular junction proteins E-cadherin and occludin was altered in the colon of Ctsk(-/-) mice, suggesting potential impairment of the barrier function. Thus, we used an ex vivo method for assessing the mucus layers and showed that the absence of cathepsin K had no influence on mucus organization and growth. The data of this study support the notion that cathepsin K contributes to intestinal homeostasis and tissue architecture, but the lack of cathepsin K activity is not expected to affect the mucus-depending barrier functions of the mouse colon. These results are important with regard to oral administration of cathepsin K inhibitors that are currently under investigation in clinical trials.
引用
收藏
页码:1391 / 1403
页数:13
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