Junior Research Group Cellular Immunobiology, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, Beutenbergstr. 11a, D-07745 Jena, Germany.
Mol Immunol. 2011 Sep;48(15-16):2135-43. doi: 10.1016/j.molimm.2011.07.007. Epub 2011 Aug 4.
Candida albicans is an opportunistic human-pathogenic fungus, which can cause superficial but also life-threatening invasive infections. The pH-regulated antigen 1 (Pra1) of C. albicans is a surface-associated and secreted protein highly expressed in the hyphal form. Pra1 can bind to complement receptor 3 (CD11b/CD18) and can mediate adhesion to and migration of human phagocytes. Here, we investigated the role of Pra1 in the activation of human neutrophils. A C. albicans mutant strain lacking Pra1 (pra1Δ) supported neutrophil migration to a lower extent than did the parental wild-type strain. A Pra1-overexpressing C. albicans strain enhanced neutrophil migration and adherence. While inactivated hyphae of the Pra1-overexpressing mutant with surface-associated Pra1 enhanced the production and release of reactive oxygen species, myeloperoxidase, lactoferrin, and interleukin 8 by neutrophils, such responses were reduced when stimulated with inactivated hyphae of the pra1Δ strain. However, Pra1-overexpressing living hyphae, which secrete large amounts of Pra1, also caused a reduced neutrophil activation, indicating that the release of extracellular Pra1 can inhibit the activation of these innate immune cells. Similarly, soluble recombinant Pra1 inhibited the neutrophil responses elicited by cell-wall bound Pra1. Finally, fungal cells lacking Pra1 were more efficiently killed by neutrophils. In conclusion, surface-exposed Pra1 plays a role in the recognition of C. albicans, especially hyphal cells, by human neutrophils and enhances neutrophil antimicrobial responses. However, the fungus can counteract some of these defense mechanisms by releasing soluble Pra1.
白色念珠菌是一种机会性人类病原真菌,可引起浅表但危及生命的侵袭性感染。白色念珠菌的 pH 调节抗原 1(Pra1)是一种表面相关的分泌蛋白,在菌丝形式中高度表达。Pra1 可以与补体受体 3(CD11b/CD18)结合,并介导与人类吞噬细胞的黏附和迁移。在这里,我们研究了 Pra1 在人类中性粒细胞激活中的作用。缺乏 Pra1 的白色念珠菌突变株(pra1Δ)比亲本野生型菌株支持中性粒细胞迁移的程度要低。Pra1 过表达的白色念珠菌菌株增强了中性粒细胞的迁移和黏附。虽然表面结合的 Pra1 的 Pra1 过表达突变体的失活菌丝增强了中性粒细胞产生和释放活性氧、髓过氧化物酶、乳铁蛋白和白细胞介素 8,但当用 pra1Δ 菌株的失活菌丝刺激时,这些反应会减少。然而,分泌大量 Pra1 的 Pra1 过表达活菌丝也会导致中性粒细胞激活减少,表明细胞外 Pra1 的释放可以抑制这些先天免疫细胞的激活。同样,可溶性重组 Pra1 抑制了细胞壁结合的 Pra1 引发的中性粒细胞反应。最后,缺乏 Pra1 的真菌细胞更容易被中性粒细胞杀死。总之,暴露于表面的 Pra1 在人类中性粒细胞识别白色念珠菌(特别是菌丝细胞)中发挥作用,并增强中性粒细胞的抗菌反应。然而,真菌可以通过释放可溶性 Pra1 来对抗其中一些防御机制。