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WNK1激酶对足细胞和肾小球毛细血管壁结构及弹性的调控

Control of Podocyte and Glomerular Capillary Wall Structure and Elasticity by WNK1 Kinase.

作者信息

Liu Zhenan, Yoon Joonho, Wichaidit Chonlarat, Jaykumar Ankita B, Dbouk Hashem A, Embry Addie E, Liu Liping, Henderson Joel M, Chang Audrey N, Cobb Melanie H, Miller Richard Tyler

机构信息

Department of Internal Medicine, Division of Nephrology, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Medicine Service, VA North Texas Health Care System, Dallas, TX, United States.

出版信息

Front Cell Dev Biol. 2021 Feb 2;8:618898. doi: 10.3389/fcell.2020.618898. eCollection 2020.

Abstract

Cytoskeletal structure and its regulation are essential for maintenance of the differentiated state of specific types of cells and their adaptation to physiologic and pathophysiologic conditions. Renal glomerular capillaries, composed of podocytes, endothelial cells, and the glomerular basement membrane, have distinct structural and biophysical properties and are the site of injury in many glomerular diseases. Calcineurin inhibitors, immunosuppressant drugs used for organ transplantation and auto-immune diseases, can protect podocytes and glomerular capillaries from injury by preserving podocyte cytoskeletal structure. These drugs cause complications including hypertension and hyperkalemia which are mediated by WNK (With No Lysine) kinases as well as vasculopathy with glomerulopathy. WNK kinases and their target kinases oxidative stress-responsive kinase 1 (OSR1) and SPS1-related proline/alanine-rich kinase (SPAK) have fundamental roles in angiogenesis and are activated by calcineurin inhibitors, but the actions of these agents on kidney vasculature, and glomerular capillaries are not fully understood. We investigated WNK1 expression in cultured podocytes and isolated mouse glomerular capillaries to determine if WNK1 contributes to calcineurin inhibitor-induced preservation of podocyte and glomerular structure. WNK1 and OSR1/SPAK are expressed in podocytes, and in a pattern similar to podocyte synaptopodin in glomerular capillaries. Calcineurin inhibitors increased active OSR1/SPAK in glomerular capillaries, the Young's modulus (E) of glomeruli, and the F/G actin ratio, effects all blocked by WNK inhibition. In glomeruli, WNK inhibition caused reduced and irregular synaptopodin-staining, abnormal capillary and foot process structures, and increased deformability. In cultured podocytes, FK506 activated OSR1/SPAK, increased lamellipodia, accelerated cell migration, and promoted traction force. These actions of FK506 were reduced by depletion of WNK1. Collectively, these results demonstrate the importance of WNK1 in regulation of the podocyte actin cytoskeleton, biophysical properties of glomerular capillaries, and slit diaphragm structure, all of which are essential to normal kidney function.

摘要

细胞骨架结构及其调节对于维持特定类型细胞的分化状态以及它们对生理和病理生理条件的适应至关重要。由足细胞、内皮细胞和肾小球基底膜组成的肾小球毛细血管具有独特的结构和生物物理特性,并且是许多肾小球疾病的损伤部位。钙调神经磷酸酶抑制剂是用于器官移植和自身免疫性疾病的免疫抑制药物,可通过保留足细胞细胞骨架结构来保护足细胞和肾小球毛细血管免受损伤。这些药物会引起包括高血压和高钾血症在内的并发症,这些并发症由WNK(无赖氨酸)激酶介导,以及伴有肾小球病的血管病变。WNK激酶及其靶激酶氧化应激反应激酶1(OSR1)和SPS1相关脯氨酸/丙氨酸丰富激酶(SPAK)在血管生成中起重要作用,并被钙调神经磷酸酶抑制剂激活,但这些药物对肾脏血管和肾小球毛细血管的作用尚未完全了解。我们研究了培养的足细胞和分离的小鼠肾小球毛细血管中WNK1的表达,以确定WNK1是否有助于钙调神经磷酸酶抑制剂诱导的足细胞和肾小球结构的保留。WNK1和OSR1/SPAK在足细胞中表达,并且在肾小球毛细血管中的表达模式与足细胞突触素相似。钙调神经磷酸酶抑制剂增加了肾小球毛细血管中活性OSR1/SPAK、肾小球的杨氏模量(E)和F/G肌动蛋白比率,所有这些作用都被WNK抑制所阻断。在肾小球中,WNK抑制导致突触素染色减少和不规则、毛细血管和足突结构异常以及变形性增加。在培养的足细胞中,FK506激活OSR1/SPAK、增加片状伪足、加速细胞迁移并促进牵引力。WNK1的缺失降低了FK506的这些作用。总体而言,这些结果证明了WNK1在调节足细胞肌动蛋白细胞骨架、肾小球毛细血管的生物物理特性和裂孔隔膜结构中的重要性,所有这些对于正常肾功能都是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e634/7884762/b0495b70843a/fcell-08-618898-g001.jpg

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