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Expression and localization of HSD17B13 along mouse urinary tract.
Zhang, Haibo; Chang, Jiazhen; Dai, Zhihong; Wang, Qiuming; Qiao, Rongfang; Huang, Yingzhi; Ma, Beibei; Jiang, Jiuchao; Zhu, Chunhua; Su, Wen; Zhang, Xiaoyan; Guan, Youfei.
Affiliation
  • Zhang H; Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, People's Republic of China.
  • Chang J; Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, People's Republic of China.
  • Dai Z; Department of Urology, The Second Hospital of Dalian Medical University, Dalian, People's Republic of China.
  • Wang Q; Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, People's Republic of China.
  • Qiao R; Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, People's Republic of China.
  • Huang Y; Health Science Center, East China Normal University, Shanghai, People's Republic of China.
  • Ma B; Health Science Center, East China Normal University, Shanghai, People's Republic of China.
  • Jiang J; Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, People's Republic of China.
  • Zhu C; Health Science Center, East China Normal University, Shanghai, People's Republic of China.
  • Su W; Department of Pathology, Health Science Center, Shenzhen University, Shenzhen, People's Republic of China.
  • Zhang X; Health Science Center, East China Normal University, Shanghai, People's Republic of China.
  • Guan Y; Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, People's Republic of China.
Am J Physiol Renal Physiol ; 327(1): F146-F157, 2024 Jul 01.
Article in En | MEDLINE | ID: mdl-38779753
ABSTRACT
17ß-Hydroxysteroid dehydrogenase-13 (HSD17B13), a newly identified lipid droplet-associated protein, plays an important role in the development of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). Emerging evidence demonstrates that NASH is an independent risk factor for chronic kidney disease, which is frequently accompanied by renal lipid accumulation. In addition, the HSD17B13 rs72613567 variant is associated with lower levels of albuminuria in patients with biopsy-proven NAFLD. At present, the role of HSD17B13 in lipid accumulation in the kidney is unclear. This study utilized bioinformatic and immunostaining approaches to examine the expression and localization of HSD17B13 along the mouse urinary tract. We found that HSD17B13 is constitutively expressed in the kidney, ureter, and urinary bladder. Our findings reveal for the first time, to our knowledge, the precise localization of HSD17B13 in the mouse urinary system, providing a basis for further studying the pathogenesis of HSD17B13 in various renal and urological diseases.NEW & NOTEWORTHY HSD17B13, a lipid droplet-associated protein, is crucial in nonalcoholic fatty liver disease (NAFLD) development. NAFLD also independently raises chronic kidney disease (CKD) risk, often with renal lipid buildup. However, HSD17B13's role in CKD-related lipid accumulation is unclear. This study makes the first effort to examine HSD17B13 expression and localization along the urinary system, providing a basis for exploring its physiological and pathophysiological roles in the kidney and urinary tract.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: 17-Hydroxysteroid Dehydrogenases / Mice, Inbred C57BL Limits: Animals Language: En Journal: Am J Physiol Renal Physiol Journal subject: FISIOLOGIA / NEFROLOGIA Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: 17-Hydroxysteroid Dehydrogenases / Mice, Inbred C57BL Limits: Animals Language: En Journal: Am J Physiol Renal Physiol Journal subject: FISIOLOGIA / NEFROLOGIA Year: 2024 Document type: Article