| First Author | Siegerist F | Year | 2024 |
| Journal | iScience | Volume | 27 |
| Issue | 12 | Pages | 111329 |
| PubMed ID | 39640577 | Mgi Jnum | J:359192 |
| Mgi Id | MGI:7786221 | Doi | 10.1016/j.isci.2024.111329 |
| Citation | Siegerist F, et al. (2024) The role of the tricellular junction protein ILDR2 in glomerulopathies: Expression patterns and functional insights. iScience 27(12):111329 |
| abstractText | The tricellular tight junctions are crucial for the regulation of paracellular flux at tricellular junctions, where tricellulin (MARVELD2) and angulins (ILDR1, ILDR2, or LSR) are localized. The role of ILDR2 in podocytes, specialized epithelial cells in the kidney, is still unknown. We investigated the role of ILDR2 in glomeruli and its influence on blood filtration. Western blots, single-cell RNA sequencing (scRNA-seq), and superresolution microscopy showed a strong expression of ILDR2 in podocytes that colocalized with the podocyte-specific claudin CLDN5. Co-immunoprecipitation revealed that ILDR2 interacts with CLDN5. In glomerulopathies, induced by nephrotoxic serum and by desoxycorticosterone acetate (DOCA)-salt heminephrectomy, ILDR2 was strongly up-regulated. Furthermore, Ildr2 knockout mice exhibited glomerular hypertrophy and decreased podocyte density. However, they did not develop effacement of podocyte foot processes or proteinuria. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) proteomic analysis of isolated glomeruli showed an increase in matrix proteins, such as fibronectin and collagens. This suggests a protective role of ILDR2 in glomerulopathies. |
