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1型糖尿病早期雌性而非雄性小鼠肾髓质中NOX-4增加:活性氧在集合管细胞中TGF-β1和纤连蛋白上调中的潜在作用

Increased Renal Medullary NOX-4 in Female but Not Male Mice during the Early Phase of Type 1 Diabetes: Potential Role of ROS in Upregulation of TGF-β1 and Fibronectin in Collecting Duct Cells.

作者信息

Casado-Barragán Felipe, Lazcano-Páez Geraldine, Larenas Paulina E, Aguirre-Delgadillo Monserrat, Olivares-Aravena Fernanda, Witto-Oyarce Daniela, Núñez-Allimant Camila, Silva Katherin, Nguyen Quynh My, Cárdenas Pilar, Kassan Modar, Gonzalez Alexis A

机构信息

Institute of Chemisry, Pontificia Universidad Católica de Valparaíso, Valparaíso 2950, Chile.

Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA 92093, USA.

出版信息

Antioxidants (Basel). 2023 Mar 16;12(3):729. doi: 10.3390/antiox12030729.

Abstract

Chronic diabetes mellitus (DM) can lead to kidney damage associated with increased reactive oxygen species (ROS), proteinuria, and tubular damage. Altered protein expression levels of transforming growth factor-beta 1 (TGF-β1), fibronectin, and renal NADPH oxidase (NOX-4) are associated with the profibrotic phenotype in renal tubular cells. NOX-4 is one of the primary sources of ROS in the diabetic kidney and responsible for the induction of profibrotic factors in collecting duct (CD) cells. The renal medulla is predominantly composed of CDs; in DM, these CD cells are exposed to high glucose (HG) load. Currently there is no published literature describing the expression of these markers in the renal medulla in male and female mice during the early phase of DM, or the role of NOX-4-induced ROS. Our aim was to evaluate changes in transcripts and protein abundances of TGF-β1, fibronectin, and NOX-4 along with ROS levels in renal medullary tissues from male and female mice during a short period of streptozotocin (STZ)-induced type 1 DM and the effect of HG in cultured CD cells. CF-1 mice were injected with or without a single dose of STZ (200 mg/kg) and euthanized at day 6. STZ females showed higher expression of fibronectin and TGF-β1 when compared to control mice of either gender. Interestingly, STZ female mice showed a >30-fold increase on mRNA levels and a 3-fold increase in protein levels of kidney medullary NOX-4. Both male and female STZ mice showed increased intrarenal ROS. In primary cultures of inner medullary CD cells exposed to HG over 48 h, the expression of TGF-β1, fibronectin, and NOX-4 were augmented. M-1 CD cells exposed to HG showed increased ROS, fibronectin, and TGF-β1; this effect was prevented by NOX-4 inhibition. Our data suggest that at as early as 6 days of STZ-induced DM, the expression of profibrotic markers TGF-β1 and fibronectin increases in renal medullary CD cells. Antioxidants mechanisms in male and female in renal medullary tissues seems to be differentially regulated by the actions of NOX-4.

摘要

慢性糖尿病(DM)可导致与活性氧(ROS)增加、蛋白尿和肾小管损伤相关的肾脏损害。转化生长因子-β1(TGF-β1)、纤连蛋白和肾NADPH氧化酶(NOX-4)的蛋白质表达水平改变与肾小管细胞的促纤维化表型相关。NOX-4是糖尿病肾脏中ROS的主要来源之一,负责诱导集合管(CD)细胞中的促纤维化因子。肾髓质主要由集合管组成;在糖尿病中,这些集合管细胞暴露于高糖(HG)负荷下。目前尚无公开文献描述在糖尿病早期雄性和雌性小鼠肾髓质中这些标志物的表达情况,或NOX-4诱导的ROS的作用。我们的目的是评估在链脲佐菌素(STZ)诱导的1型糖尿病短时间内,雄性和雌性小鼠肾髓质组织中TGF-β1、纤连蛋白和NOX-4的转录本和蛋白质丰度变化以及ROS水平,以及高糖对培养的集合管细胞的影响。CF-1小鼠注射或不注射单剂量STZ(200 mg/kg),并在第6天安乐死。与任何性别的对照小鼠相比,STZ处理的雌性小鼠纤连蛋白和TGF-β1的表达更高。有趣的是,STZ雌性小鼠肾髓质NOX-4的mRNA水平增加了3​​0倍以上,蛋白质水平增加了3倍。雄性和雌性STZ小鼠的肾内ROS均增加。在暴露于高糖超过48小时的内髓集合管细胞原代培养物中,TGF-β1、纤连蛋白和NOX-4的表达增加。暴露于高糖的M-1集合管细胞显示ROS、纤连蛋白和TGF-β1增加;这种作用可被NOX-4抑制所阻止。我们的数据表明,在STZ诱导的糖尿病早期6天,促纤维化标志物TGF-β1和纤连蛋白在肾髓质集合管细胞中的表达增加。肾髓质组织中雄性和雌性的抗氧化机制似乎受NOX-4作用的差异调节。

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