Schade Jutta, Stephan Michael, Schmiedl Andreas, Wagner Leona, Niestroj André J, Demuth Hans-Ulrich, Frerker Nadine, Klemann Christian, Raber Kerstin A, Pabst Reinhard, von Hörsten Stephan
Department of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
J Histochem Cytochem. 2008 Feb;56(2):147-55. doi: 10.1369/jhc.7A7319.2007. Epub 2007 Oct 29.
The expression of dipeptidyl peptidase 4 (DP4, CD26) affects T-cell recruitment to lungs in an experimental rat asthma model. Furthermore, the gene of the structural homologous DP10 represents a susceptibility locus for asthma in humans, and the functional homologous DP8/9 are expressed in human leukocytes. Thus, although several mechanisms may account for a role of DP4-like peptidases in asthma, detailed information on their anatomical sites of expression and function in lungs is lacking. Therefore, bronchi and lung parenchyma were evaluated using immunohistochemistry and histochemical/enzymatic activity assays, as well as quantitative real-time PCR for this family of peptidases in naïve and asthmatic rat lungs derived from wild-type F344 and DP4-deficient F344 rat strains. Surprisingly, results show not only that the induction of experimental asthma increases DP4 enzymatic activity in the bronchoalveolar lavage fluid and parenchyma, but also that DP8/9 enzymatic activity is regulated and, as well as the expression of DP10, primarily found in the bronchial epithelium of the airways. This is the first report showing a differential and site-specific DP4-like expression and function in the lungs, suggesting a pathophysiologically significant role in asthma.
在实验性大鼠哮喘模型中,二肽基肽酶4(DP4,CD26)的表达影响T细胞向肺的募集。此外,结构同源物DP10的基因是人类哮喘的一个易感基因座,功能同源物DP8/9在人类白细胞中表达。因此,尽管几种机制可能解释了DP4样肽酶在哮喘中的作用,但关于它们在肺中的表达解剖部位和功能的详细信息仍然缺乏。因此,使用免疫组织化学、组织化学/酶活性测定以及定量实时PCR,对来自野生型F344和DP4缺陷型F344大鼠品系的未致敏和哮喘大鼠肺中的该肽酶家族进行了支气管和肺实质评估。令人惊讶的是,结果不仅表明实验性哮喘的诱导增加了支气管肺泡灌洗液和实质中的DP4酶活性,而且DP8/9酶活性也受到调节,并且DP10的表达主要在气道的支气管上皮中发现。这是第一份显示肺中存在差异性和位点特异性DP4样表达及功能的报告,表明其在哮喘病理生理学中具有重要作用。