Diversities of podocyte molecular changes induced by different antiproteinuria drugs
- PMID: 16636307
- DOI: 10.1177/153537020623100513
Diversities of podocyte molecular changes induced by different antiproteinuria drugs
Abstract
Nephrin, podocin, CD2AP, and alpha-actinin-4 are important podocyte proteins that help maintain the integrity of the slit diaphragm and prevent proteinuria. Studies have shown that angiotensin-converting enzyme inhibitors, glucocorticoids, and all-trans retinoic acid (ATRA) have antiproteinuric effects. However, it is still unclear whether these drugs, with different pharmacological mechanisms, lead to a reduction in proteinuria by changing the expression and distribution of these important podocyte proteins. In this study, changes in the expression and distribution of nephrin, podocin, CD2AP, and alpha-actinin-4 were dynamically detected in Adriamycin-induced nephrotic (ADR) rats treated with three different drugs: lisinopril, prednisone, and ATRA. Nephropathy was induced by an intravenous injection of Adriamycin. After Adriamycin injection, rats received lisinopril, prednisone, and ATRA treatment, respectively. Renal tissues were collected at Days 3, 7, 14, and 28. The distribution and the expression of messenger RNA and protein of nephrin, podocin, CD2AP, and alpha-actinin-4 were detected by indirect immunofluorescence, real-time polymerase chain reaction, and Western blotting, respectively. With the intervention of lisinopril, prednisone, and ATRA, changes in the expression of nephrin, podocin, and CD2AP were diverse, which was different from that detected in ADR rats. After lisinopril and prednisone intervention, podocin exhibited prominent earlier changes compared with those of nephrin and CD2AP, whereas CD2AP showed more prominent changes after ATRA intervention. There was no change in the expression of alpha-actinin-4 molecule. In summary, we conclude that the antiproteinuric effects of lisinopril, prednisone, and ATRA were achieved by changes in the expression and distribution of the important podocyte molecules nephrin, podocin, CD2AP, and alpha-actinin-4. The pattern in the change of podocyte molecules after lisinopril and prednisone intervention was similar, but the pattern in the change of podocyte molecules after ATRA intervention was different from that of lisinopril or prednisone intervention.
Similar articles
-
Key molecular events in puromycin aminonucleoside nephrosis rats.Pathol Int. 2004 Sep;54(9):703-11. doi: 10.1111/j.1440-1827.2004.01683.x. Pathol Int. 2004. PMID: 15363039
-
The relationship among nephrin, podocin, CD2AP, and alpha-actinin might not be a true 'interaction' in podocyte.Kidney Int. 2006 Apr;69(7):1207-15. doi: 10.1038/sj.ki.5000245. Kidney Int. 2006. PMID: 16501493
-
[Relationship between podocyte molecule's distribution and expression, foot process morphology and proteinuria].Beijing Da Xue Xue Bao Yi Xue Ban. 2004 Apr;36(2):139-44. Beijing Da Xue Xue Bao Yi Xue Ban. 2004. PMID: 15100730 Chinese.
-
CD2-associated protein and glomerular disease.Lancet. 2003 Nov 22;362(9397):1746-8. doi: 10.1016/S0140-6736(03)14856-8. Lancet. 2003. PMID: 14643126 Review.
-
[Structure and function of the glomerular filtration barrier].Pol Merkur Lekarski. 2005 Mar;18(105):317-20. Pol Merkur Lekarski. 2005. PMID: 15997642 Review. Polish.
Cited by
-
Protective effect of sulodexide on podocyte injury in adriamycin nephropathy rats.J Huazhong Univ Sci Technolog Med Sci. 2009 Dec;29(6):715-9. doi: 10.1007/s11596-009-0608-0. Epub 2009 Dec 29. J Huazhong Univ Sci Technolog Med Sci. 2009. PMID: 20037813
-
Induction of podocyte VEGF164 overexpression at different stages of development causes congenital nephrosis or steroid-resistant nephrotic syndrome.Am J Pathol. 2010 Nov;177(5):2225-33. doi: 10.2353/ajpath.2010.091146. Epub 2010 Sep 9. Am J Pathol. 2010. PMID: 20829436 Free PMC article.
-
Cytoskeleton Rearrangement in Podocytopathies: An Update.Int J Mol Sci. 2024 Jan 4;25(1):647. doi: 10.3390/ijms25010647. Int J Mol Sci. 2024. PMID: 38203817 Free PMC article. Review.
-
All-trans retinoic acid up-regulates the human CD2AP gene expression through Sp1/Sp3 binding sites.Immunol Res. 2015 Jul;62(3):273-9. doi: 10.1007/s12026-015-8658-9. Immunol Res. 2015. PMID: 25957888
-
The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models.Life (Basel). 2023 Jan 19;13(2):277. doi: 10.3390/life13020277. Life (Basel). 2023. PMID: 36836636 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous