Chou Y C, Luttge W G, Sumners C
Department of Neuroscience, University of Florida College of Medicine, Gainesville 32610.
Brain Res Dev Brain Res. 1991 Jul 16;61(1):55-61. doi: 10.1016/0165-3806(91)90113-w.
In the present study we have examined the expression of mineralocorticoid Type I and glucocorticoid Type II receptors in astrocyte glia maintained in culture for different periods of time. Cytosolic mineralocorticoid Type I receptors were labeled with [3H]aldosterone (ALDO) in the presence of a 500-fold molar excess of the potent Type II receptor ligand RU 28362. [3H]Dexamethasone (DEX) was used to label cytosolic Type II receptors. Both Type I and Type II receptor binding was saturable in astrocyte glia that had been maintained in culture for 20 and 30 days following final plating (i.e. 20- and 30-day-old cultures). Scatchard analysis of [3H]ALDO binding revealed a single class of Type I receptors, with dissociation constants (Kd) of 0.45 +/- 0.13 nM and 0.53 +/- 0.07 nM, respectively, in 20- and 30-day-old cultures. The number of Type I receptors in 30-day-old cultures was nearly half that found in 20-day-old cultures (22.06 vs 42.64 fmol/mg protein). Linear Scatchard plots were also obtained for [3H]DEX binding to cytosol prepared from 20- and 30-day-old cultures. There were no significant differences in the Kd or Bmax values for [3H]DEX binding in 20- or 30-day-old cultures, i.e. 2.06 +/- 0.15 nM and 247.36 +/- 18.16 fmol/mg protein for 20-day-old cells and 2.3 +/- 0.74 nM and 261.02 +/- 3.08 fmol/mg protein for 30-day-old cells. These Bmax values are more than double the Bmax value for [3H]DEX binding observed in our previous studies in 10-day-old astrocyte glial cultures. Switching cultured astrocyte glial from serum-supplemented to serum-free medium had no significant effects on the Kd values of Type I or Type II receptors in all the cultures tested. However, treatment with serum-free medium increased the number of Type I receptors in 30-day-old cultures to a level similar to that found in 20-day-old cultures. Taken together, these binding data suggest that Type I and Type II receptors are expressed differently in astrocyte glia as a function of time in culture.
在本研究中,我们检测了在不同培养时间段的星形胶质细胞中盐皮质激素Ⅰ型受体和糖皮质激素Ⅱ型受体的表达。在存在500倍摩尔过量的强效Ⅱ型受体配体RU 28362的情况下,用[³H]醛固酮(ALDO)标记胞质盐皮质激素Ⅰ型受体。用[³H]地塞米松(DEX)标记胞质Ⅱ型受体。在最终接种后培养20天和30天的星形胶质细胞(即20日龄和30日龄培养物)中,Ⅰ型和Ⅱ型受体结合均具有饱和性。对[³H]ALDO结合进行Scatchard分析显示,在20日龄和30日龄培养物中分别有一类Ⅰ型受体,解离常数(Kd)分别为0.45±0.13 nM和0.53±0.07 nM。30日龄培养物中Ⅰ型受体的数量几乎是20日龄培养物中的一半(22.06对42.64 fmol/mg蛋白质)。对于[³H]DEX与从20日龄和30日龄培养物制备的胞质溶胶的结合,也获得了线性Scatchard图。在20日龄或30日龄培养物中,[³H]DEX结合的Kd或Bmax值没有显著差异,即20日龄细胞的Kd为2.06±0.15 nM,Bmax为247.36±18.16 fmol/mg蛋白质;30日龄细胞的Kd为2.3±0.74 nM,Bmax为261.02±3.08 fmol/mg蛋白质。这些Bmax值比我们之前在10日龄星形胶质细胞培养物中观察到的[³H]DEX结合的Bmax值高出一倍多。将培养的星形胶质细胞从补充血清的培养基转换为无血清培养基,对所有测试培养物中Ⅰ型或Ⅱ型受体的Kd值没有显著影响。然而,用无血清培养基处理使30日龄培养物中Ⅰ型受体的数量增加到与20日龄培养物中相似的水平。综上所述,这些结合数据表明,Ⅰ型和Ⅱ型受体在星形胶质细胞中的表达随培养时间而有所不同。