Fetal Programming Laboratory, Morphology Department, São Paulo State University, Botucatu, São Paulo, Brazil.
PLoS One. 2013 Aug 19;8(8):e71310. doi: 10.1371/journal.pone.0071310. eCollection 2013.
Prior study shows that maternal protein-restricted (LP) 16-wk-old offspring have pronounced reduction of nephron number and arterial hypertension associated with unchanged glomerular filtration rate, besides enhanced glomerular area, which may be related to glomerular hyperfiltration/overflow and which accounts for the glomerular filtration barrier breakdown and early glomerulosclerosis. In the current study, LP rats showed heavy proteinuria associated with podocyte simplification and foot process effacement. TGF-β1 glomerular expression was significantly enhanced in LP. Isolated LP glomeruli show a reduced level of miR-200a, miR-141, miR-429 and ZEB2 mRNA and upregulated collagen 1α1/2 mRNA expression. By western blot analyzes of whole kidney tissue, we found significant reduction of both podocin and nephrin and enhanced expression of mesenchymal protein markers such as desmin, collagen type I and fibronectin. From our present knowledge, these are the first data showing renal miRNA modulation in the protein restriction model of fetal programming. The fetal-programmed adult offspring showed pronounced structural glomerular disorders with an accentuated and advanced stage of fibrosis, which led us to state that the glomerular miR-200 family would be downregulated by TGF-β1 action inducing ZEB 2 expression that may subsequently cause glomeruli epithelial-to-mesenchymal transition.
先前的研究表明,母源性蛋白质限制(LP)16 周龄的后代的肾单位数量明显减少,同时伴有动脉高血压,但肾小球滤过率不变,此外肾小球面积增加,这可能与肾小球高滤过/超负荷有关,是肾小球滤过屏障破坏和早期肾小球硬化的原因。在本研究中,LP 大鼠表现出大量蛋白尿,伴有足细胞简化和足突消失。LP 肾小球中 TGF-β1 的表达显著增强。分离的 LP 肾小球显示 miR-200a、miR-141、miR-429 和 ZEB2mRNA 水平降低,胶原 1α1/2mRNA 表达上调。通过对全肾组织的 Western blot 分析,我们发现 podocin 和 nephrin 的表达明显减少,间充质蛋白标志物如结蛋白、I 型胶原和纤维连接蛋白的表达增强。就我们目前的知识而言,这些是首次在胎儿编程的蛋白质限制模型中显示肾脏 miRNA 调节的研究数据。胎儿编程的成年后代表现出明显的结构性肾小球病变,纤维化程度加重且处于更高级阶段,这使我们认为肾小球 miR-200 家族可能会被 TGF-β1 诱导的 ZEB2 表达下调,从而导致肾小球上皮细胞向间充质转化。