Signaling mechanisms in renal compensatory hypertrophy revealed by multi-omics

被引:14
|
作者
Kikuchi, Hiroaki [1 ]
Chou, Chung-Lin [1 ]
Yang, Chin-Rang [1 ]
Chen, Lihe [1 ]
Jung, Hyun Jun [2 ]
Park, Euijung [1 ]
Limbutara, Kavee [3 ]
Carter, Benjamin [4 ]
Yang, Zhi-Hong [5 ]
Kun, Julia F. [5 ]
Remaley, Alan T. [5 ]
Knepper, Mark A. [1 ]
机构
[1] NHLBI, Epithelial Syst Biol Lab, Syst Biol Ctr, Bethesda, MD 20824 USA
[2] Johns Hopkins Univ, Dept Med, Div Nephrol, Sch Med, Baltimore, MD USA
[3] Chulalongkorn Univ, Fac Med, Ctr Excellence Syst Biol, Bangkok, Thailand
[4] NHLBI, Syst Biol Ctr, Lab Epigenome Biol, Bethesda, MD USA
[5] NHLBI, Lipoprotein Metab Sect, Translat Vasc Med Branch, NIH, Bethesda, MD USA
关键词
PROLIFERATOR-ACTIVATED RECEPTORS; METABOLIC-RESPONSE; MAMMALIAN TARGET; FATTY-ACIDS; GENE; NEPHRON; ALPHA; EICOSANOIDS; ADAPTATION; EXPRESSION;
D O I
10.1038/s41467-023-38958-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Loss of a kidney results in compensatory growth of the remaining kidney, a phenomenon of considerable clinical importance. However, the mechanisms involved are largely unknown. Here, we use a multi-omic approach in a unilateral nephrectomy model in male mice to identify signaling processes associated with renal compensatory hypertrophy, demonstrating that the lipid-activated transcription factor peroxisome proliferator-activated receptor alpha (PPAR & alpha;) is an important determinant of proximal tubule cell size and is a likely mediator of compensatory proximal tubule hypertrophy. The authors used a multi-omic approach in a mouse unilateral nephrectomy model to identify signaling processes associated with compensatory hypertrophy of the renal proximal tubule. The results indicate that PPAR & alpha; is an important determinant of proximal tubule cell size and is a likely mediator of compensatory proximal tubule hypertrophy.
引用
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页数:22
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