Vaughan Michael R, Pippin Jeffrey W, Griffin Siân V, Krofft Ron, Fleet Margaret, Haseley Leah, Shankland Stuart J
Department of Medicine, Division of Nephrology, University of Washington, Seattle, Washington, USA.
Kidney Int. 2005 Jul;68(1):133-44. doi: 10.1111/j.1523-1755.2005.00387.x.
Podocytes are terminally differentiated and highly specialized epithelial cells. The factors governing podocyte differentiation are poorly understood. We tested the hypothesis that all-trans retinoic acid (ATRA), a vitamin A derivative, induces podocyte differentiation in vitro and in vivo.
We tested the effects of ATRA on podocytes. Primary rat, primary mouse, and immortalized mouse podocytes were exposed to ATRA (1, 5, 10, 20, 40, 50, 80, 160, and 200 micromol/L) or control (ethanol) for 72 hours. Cell morphology was examined by electron microscopy, the expression of podocyte specific proteins was measured by immunoflourescence and Western blot analysis, cell number and apoptosis were measured by 3-[4,5] dimethylthiazol-2,5-diphenyltetrazolium bromide (MTT) assay and Hoechst staining, respectively. To determine if ATRA alters podocyte differentiation in vivo, experimental injury was induced in C57BL6 mice using the antiglomerular antibody. Animals were given either daily intraperitoneal ATRA (16 mg/kg) or vehicle (corn oil). For end points, we measured proteinuria, podocyte-specific protein immunostaining, and proliferation [proliferating cell nuclear antigen (PCNA)] at days 5 and 14 (N= 5/group/time point).
ATRA induced podocyte process formation in vitro, and significantly increased the expression of nephrin and podocin. This coincided with a reduction in proliferation. ATRA also significantly prevented the decrease in staining for synaptopodin, nephrin, and podocin in experimental animals (P < 0.05 vs. control). This was accompanied by reduced proteinuria and decreased podocyte proliferation (P < 0.05 vs. control).
ATRA induces podocyte differentiation in vitro and in vivo and alters the expression of certain podocyte-specific proteins. Further studies are ongoing to delineate the mechanism of this effect.
足细胞是终末分化且高度特化的上皮细胞。目前对调控足细胞分化的因素了解甚少。我们检验了一种假设,即全反式维甲酸(ATRA),一种维生素A衍生物,可在体外和体内诱导足细胞分化。
我们检测了ATRA对足细胞的影响。将原代大鼠、原代小鼠和永生化小鼠足细胞暴露于ATRA(1、5、10、20、40、50、80、160和200 μmol/L)或对照(乙醇)中72小时。通过电子显微镜检查细胞形态,通过免疫荧光和蛋白质印迹分析测量足细胞特异性蛋白的表达,分别通过3-[4,5]二甲基噻唑-2,5-二苯基四氮唑溴盐(MTT)法和Hoechst染色测量细胞数量和凋亡。为了确定ATRA是否在体内改变足细胞分化,使用抗肾小球抗体在C57BL6小鼠中诱导实验性损伤。给动物每日腹腔注射ATRA(16 mg/kg)或赋形剂(玉米油)。作为终点指标,我们在第5天和第14天测量蛋白尿、足细胞特异性蛋白免疫染色和增殖[增殖细胞核抗原(PCNA)](每组/每个时间点N = 5)。
ATRA在体外诱导足细胞突起形成,并显著增加nephrin和podocin的表达。这与增殖减少相吻合。ATRA还显著防止了实验动物中突触足蛋白、nephrin和podocin染色的减少(与对照组相比,P < 0.05)。这伴随着蛋白尿减少和足细胞增殖降低(与对照组相比,P < 0.05)。
ATRA在体外和体内诱导足细胞分化,并改变某些足细胞特异性蛋白的表达。正在进行进一步研究以阐明这种作用的机制。