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SETD2 regulates SLC family transporter-mediated sodium and glucose reabsorptions in renal tubule.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Nov 19; Vol. 734, pp. 150730. Date of Electronic Publication: 2024 Sep 28. - Publication Year :
- 2024
-
Abstract
- A regulatory mechanism for SLC family transporters, critical transporters for sodium and glucose reabsorptions in renal tubule, is incompletely understood. Here, we report an important regulation of SLC family transporter by SETD2, a chromatin remodeling gene whose alterations have been found in a subset of kidney cancers. Kidney-specific inactivation of Setd2 resulted in hypovolemia with excessive urine excretion in mouse and interestingly, RNA-sequencing analysis of Setd2-deficient murine kidney exhibited decreased expressions of SLC family transporters, critical transporters for sodium and glucose reabsorptions in renal tubule. Importantly, inactivation of Setd2 in murine kidney displayed attenuated dapagliflozin-induced diuresis and glucose excretion, further supporting that SETD2 might regulate SLCfamily transporter-mediated sodium and glucose reabsorptions in renal tubule. These data uncover an important regulation of SLC family transporter by SETD2, which may illuminate a crosstalk between metabolism and epigenome in renal tubule.<br />Competing Interests: Declaration of competing interest The authors declare neither competing interests nor conflict of financial interest.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Mice
Male
Mice, Knockout
Solute Carrier Proteins metabolism
Solute Carrier Proteins genetics
Mice, Inbred C57BL
Renal Reabsorption
Histone-Lysine N-Methyltransferase metabolism
Histone-Lysine N-Methyltransferase genetics
Glucose metabolism
Kidney Tubules metabolism
Sodium metabolism
Sodium urine
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 734
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 39366177
- Full Text :
- https://doi.org/10.1016/j.bbrc.2024.150730