Takeuchi A, Throckmorton D C, Brogden A P, Yoshizawa N, Rasmussen H, Kashgarian M
Department of Pathology, Yale University School of Medicine, New Haven, Connecticut 06510.
Am J Physiol. 1995 Jan;268(1 Pt 2):F13-9. doi: 10.1152/ajprenal.1995.268.1.F13.
We examined the effects of periodic changes in extracellular glucose concentration on matrix production and proliferation using three groups of cultured rat mesangial cells (MCs): 1) MCs in medium with continuous 5 mM glucose (CL), 2) MCs in medium alternating daily between 5 and 25 mM glucose (PH), and 3) MCs in medium with continuous 25 mM glucose (CH). MCs cultured in PH for 10 days produced 329 and 110% more type III collagen protein than MCs cultured in CL and CH, respectively. MCs cultured in PH induced 31 and 14% more type IV collagen than MCs cultured in CL and CH, respectively. Extracellular glucose concentration had no effect on the amount of type I collagen produced. MCs cultured in PH or CH for 5 days also expressed increased levels of type I, III, and IV collagen mRNA compared with MCs cultured in CL. MCs cultured in PH for 8-10 days also produced significantly more DNA than MCs in CL or CH. These data suggest that the temporal pattern of exposure to high extracellular glucose plays a role in regulating matrix formation and cellular proliferation by MCs. Furthermore, periodic elevations of extracellular glucose had a greater stimulatory effect on collagen production than a sustained elevation. These results suggest that decreasing the variability of blood glucose concentration may decrease the adverse effect of elevated glucose levels on MC matrix production and the progression of diabetic glomerulopathy.
我们使用三组培养的大鼠系膜细胞(MCs)研究了细胞外葡萄糖浓度的周期性变化对基质产生和增殖的影响:1)在含有持续5 mM葡萄糖的培养基中的MCs(CL),2)在培养基中每天交替使用5和25 mM葡萄糖的MCs(PH),以及3)在含有持续25 mM葡萄糖的培养基中的MCs(CH)。在PH中培养10天的MCs产生的III型胶原蛋白分别比在CL和CH中培养的MCs多329%和110%。在PH中培养的MCs诱导产生的IV型胶原蛋白分别比在CL和CH中培养的MCs多31%和14%。细胞外葡萄糖浓度对I型胶原蛋白的产生量没有影响。与在CL中培养的MCs相比,在PH或CH中培养5天的MCs也表达了更高水平的I、III和IV型胶原蛋白mRNA。在PH中培养8 - 10天的MCs也比CL或CH中的MCs产生了显著更多的DNA。这些数据表明,暴露于高细胞外葡萄糖的时间模式在调节MCs的基质形成和细胞增殖中起作用。此外,细胞外葡萄糖的周期性升高对胶原蛋白产生的刺激作用比持续升高更大。这些结果表明,降低血糖浓度的变异性可能会降低血糖水平升高对MC基质产生和糖尿病肾小球病进展的不利影响。