首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Intraglomerular pressure and mesangial stretching stimulate extracellular matrix formation in the rat.
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Intraglomerular pressure and mesangial stretching stimulate extracellular matrix formation in the rat.

机译:肾小球内压力和肾小球系膜拉伸刺激大鼠细胞外基质的形成。

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摘要

To define the interplay of glomerular hypertension and hypertrophy with mesangial extracellular matrix (ECM) deposition, we examined the effects of glomerular capillary distention and mesangial cell stretching on ECM synthesis. The volume of microdissected rat glomeruli (Vg), perfused ex vivo at increasing flows, was quantified and related to the proximal intraglomerular pressure (PIP). Glomerular compliance, expressed as the slope of the positive linear relationship between PIP and Vg was 7.68 x 10(3) microns 3/mmHg. Total Vg increment (PIP 0-150 mmHg) was 1.162 x 10(6) microns 3 or 61% (n = 13). A 16% increase in Vg was obtained over the PIP range equivalent to the pathophysiological limits of mean transcapillary pressure difference. A similar effect of renal perfusion on Vg was also noted histologically in tissue from kidneys perfused/fixed in vivo. Cultured mesangial cells undergoing cyclic stretching increased their synthesis of protein, total collagen, and key components of ECM (collagen IV, collagen I, laminin, fibronectin). Synthetic rates were stimulated by cell growth and the degree of stretching. These results suggest that capillary expansion and stretching of mesangial cells by glomerular hypertension provokes increased ECM production which is accentuated by cell growth and glomerular hypertrophy. Mesangial expansion and glomerulosclerosis might result from this interplay of mechanical and metabolic forces.
机译:为了定义肾小球高血压和肥大与肾小球膜细胞外基质(ECM)沉积之间的相互作用,我们检查了肾小球毛细血管扩张和肾小球膜细胞拉伸对ECM合成的影响。显微解剖的大鼠肾小球(Vg)的体积,以增加的流量离体灌注,被量化并与近端肾小球内压力(PIP)相关。肾小球顺应性表示为PIP和Vg之间的正线性关系的斜率是7.68 x 10(3)微米3 / mmHg。总Vg增量(PIP 0-150 mmHg)为1.162 x 10(6)微米3或61%(n = 13)。在相当于平均经毛细血管压差的病理生理极限的PIP范围内,Vg增加了16%。在组织学上,在体内灌注/固定的肾脏组织中也注意到了肾脏灌注对Vg的类似作用。培养的肾小球膜细胞经过周期性拉伸,可以增加蛋白质,总胶原蛋白和ECM的关键成分(胶原蛋白IV,胶原蛋白I,层粘连蛋白,纤连蛋白)的合成。细胞生长和伸展程度刺激了合成速率。这些结果表明肾小球性高血压引起的肾小球系膜细胞的毛细血管扩张和舒张引起了细胞外生长和肾小球肥大加剧的ECM产生。系膜扩张和肾小球硬化可能是由机械力和代谢力的相互作用引起的。

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