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The Expression and Activity of Cathepsins D H and K in Asthmatic Airways

机译:的组织蛋白酶dH和K哮喘航空公司的表达和活性

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摘要

Tumstatin is an anti-angiogenic collagen IV α3 fragment, levels of which are reduced in the airways of asthmatics. Its reduction may be due to the degradation by extracellular matrix (ECM) proteases. Cathepsins play a role in ECM remodelling, with cathepsin D, H and K (CTSD, CTSH and CTSK) being associated with lung diseases. CTSD modulates the NC1 domains of collagen molecules including tumstatin, while CTSH and CTSK are involved in ECM degradation. The role of these cathepsins in the regulation of tumstatin in the lung has not previously been examined. We demonstrated that CTSB, D, F, H, K, L and S mRNA was expressed in the airways. Quantification of immunohistochemistry showed that there is no difference in the global expression of CTSD, CTSH and CTSK between asthmatics and non-asthmatics. CTSD and CTSK, but not CTSH had the capacity to degrade tumstatin. No difference was observed in the activity of CTSD and H in bronchoalveolar lavage fluid of asthmatic and non-asthmatics, while CTSK was undetectable. This indicates that while CTSD possesses the potential to directly regulate tumstatin, and thus angiogenesis through this mechanism however, it is not likely to be involved in the dysregulation of tumstatin found in asthmatic airways.
机译:Tumstatin是抗血管生成性胶原IVα3片段,在哮喘患者的气道中其水平降低。其减少可能是由于细胞外基质(ECM)蛋白酶的降解。组织蛋白酶在ECM重塑中起作用,组织蛋白酶D,H和K(CTSD,CTSH和CTSK)与肺部疾病有关。 CTSD调节包括tumstatin在内的胶原分子的NC1结构域,而CTSH和CTSK参与ECM降解。这些组织蛋白酶在调节肺抑素中的作用以前没有被检查过。我们证明了CTSB,D,F,H,K,L和S mRNA在气道中表达。免疫组化的定量显示,哮喘和非哮喘患者的CTSD,CTSH和CTSK的整体表达没有差异。 CTSD和CTSK,但没有CTSH具有降解塔格他汀的能力。在哮喘和非哮喘病患者的支气管肺泡灌洗液中,CTSD和H的活性未见差异,而未检测到CTSK。这表明,尽管CTSD具有直接调节肿瘤抑制素的潜力,并因此通过这种机制具有血管生成的潜力,但它不太可能与哮喘气道中发现的肿瘤抑制素的失调有关。

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