Dumont, Vincent ORCID: 0000-0002-2893-5479, Tolvanen, Tuomas A., Kuusela, Sara, Wang, Hong ORCID: 0000-0001-5700-6786, Nyman, Tuula A., Lindfors, Sonja, Tienari, Jukka, Nisen, Harry, Suetsugu, Shiro ORCID: 0000-0002-4612-0628, Plomann, Markus, Kawachi, Hiroshi and Lehtonen, Sanna ORCID: 0000-0003-4189-2415 (2017). PACSIN2 accelerates nephrin trafficking and is up-regulated in diabetic kidney disease. Faseb J., 31 (9). S. 3978 - 3991. BETHESDA: FEDERATION AMER SOC EXP BIOL. ISSN 1530-6860

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Abstract

Nephrin is a core component of podocyte (glomerular epithelial cell) slit diaphragm and is required for kidney ultrafiltration. Down-regulation or mislocalization of nephrin has been observed in diabetic kidney disease (DKD), characterized by albuminuria. Here, we investigate the role of protein kinase C and casein kinase 2 substrate in neurons 2 (PACSIN2), a regulator of endocytosis and recycling, in the trafficking of nephrin and development of DKD. We observe that PACSIN2 is up-regulated and nephrin mislocalized in podocytes of obese Zucker diabetic fatty (ZDF) rats that have altered renal function. In cultured podocytes, PACSIN2 and nephrin colocalize and interact. We show that nephrin is endocytosed in PACSIN2-positive membrane regions and that PACSIN2 overexpression increases both nephrin endocytosis and recycling. We identify rabenosyn-5, which is involved in early endosome maturation and endosomal sorting, as a novel interaction partner of PACSIN2. Interestingly, rabenosyn-5 expression is increased in podocytes in obese ZDF rats, and, in vitro, its overexpression enhances the association of PACSIN2 and nephrin. We also show that palmitate, which is elevated in diabetes, enhances this association. Collectively, PACSIN2 is up-regulated and nephrin is abnormally localized in podocytes of diabetic ZDF rats. In vitro, PACSIN2 enhances nephrin turnover apparently via a mechanism involving rabenosyn-5. The data suggest that elevated PACSIN2 expression accelerates nephrin trafficking and associates with albuminuria.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Dumont, VincentUNSPECIFIEDorcid.org/0000-0002-2893-5479UNSPECIFIED
Tolvanen, Tuomas A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kuusela, SaraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wang, HongUNSPECIFIEDorcid.org/0000-0001-5700-6786UNSPECIFIED
Nyman, Tuula A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lindfors, SonjaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Tienari, JukkaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nisen, HarryUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Suetsugu, ShiroUNSPECIFIEDorcid.org/0000-0002-4612-0628UNSPECIFIED
Plomann, MarkusUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kawachi, HiroshiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lehtonen, SannaUNSPECIFIEDorcid.org/0000-0003-4189-2415UNSPECIFIED
URN: urn:nbn:de:hbz:38-220710
DOI: 10.1096/fj.201601265R
Journal or Publication Title: Faseb J.
Volume: 31
Number: 9
Page Range: S. 3978 - 3991
Date: 2017
Publisher: FEDERATION AMER SOC EXP BIOL
Place of Publication: BETHESDA
ISSN: 1530-6860
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
SLIT DIAPHRAGM; MEMBRANE-TRAFFICKING; FATTY-ACIDS; PROTEIN; NEPHROPATHY; PODOCYTES; COMPLEX; INJURY; GENE; ORGANIZATIONMultiple languages
Biochemistry & Molecular Biology; Biology; Cell BiologyMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/22071

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