Department of Immunemodulation at the Dermatology, University Hospital Erlangen, Erlangen, Germany.
J Am Soc Nephrol. 2013 May;24(6):906-16. doi: 10.1681/ASN.2012020133. Epub 2013 Mar 28.
Podocytes are essential to the structure and function of the glomerular filtration barrier; however, they also exhibit increased expression of MHC class II molecules under inflammatory conditions, and they remove Ig and immune complexes from the glomerular basement membrane (GBM). This finding suggests that podocytes may act as antigen-presenting cells, taking up and processing antigens to initiate specific T cell responses, similar to professional hematopoietic cells such as dendritic cells or macrophages. Here, MHC-antigen complexes expressed exclusively on podocytes of transgenic mice were sufficient to activate CD8+ T cells in vivo. In addition, deleting MHC class II exclusively on podocytes prevented the induction of experimental anti-GBM nephritis. Podocytes ingested soluble and particulate antigens, activated CD4+ T cells, and crosspresented exogenous antigen on MHC class I molecules to CD8+ T cells. In conclusion, podocytes participate in the antigen-specific activation of adaptive immune responses, providing a potential target for immunotherapies of inflammatory kidney diseases and transplant rejection.
足细胞对于肾小球滤过屏障的结构和功能至关重要;然而,在炎症条件下,它们也会增加 MHC Ⅱ类分子的表达,并且从肾小球基底膜(GBM)中清除 Ig 和免疫复合物。这一发现表明,足细胞可能充当抗原呈递细胞,摄取和处理抗原以启动特异性 T 细胞反应,类似于树突状细胞或巨噬细胞等专业造血细胞。在这里,仅在转基因小鼠的足细胞上表达的 MHC-抗原复合物足以在体内激活 CD8+T 细胞。此外,仅在足细胞上缺失 MHC Ⅱ类分子可防止实验性抗 GBM 肾炎的诱导。足细胞摄取可溶性和颗粒性抗原,激活 CD4+T 细胞,并在 MHC Ⅰ类分子上交叉呈递外源性抗原给 CD8+T 细胞。总之,足细胞参与适应性免疫反应的抗原特异性激活,为炎症性肾脏疾病和移植排斥的免疫治疗提供了一个潜在的靶点。