Literature DB >> 1655310

Expression of mineralocorticoid type I and glucocorticoid type II receptors in astrocyte glia as a function of time in culture.

Y C Chou1, W G Luttge, C Sumners.   

Abstract

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.

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Year:  1991        PMID: 1655310     DOI: 10.1016/0165-3806(91)90113-w

Source DB:  PubMed          Journal:  Brain Res Dev Brain Res        ISSN: 0165-3806


  3 in total

1.  Corticosteroids regulate the gene expression of FGF-1 and FGF-2 in cultured rat astrocytes.

Authors:  V Magnaghi; M A Riva; I Cavarretta; L Martini; R C Melcangi
Journal:  J Mol Neurosci       Date:  2000-08       Impact factor: 3.444

2.  Morphofunctional changes of the astrocyte in rat hippocampus under different corticosteroid conditions.

Authors:  Chun-Ying Yang; Toshiyuki Matsuzaki; Norio Iijima; Naoko Kajimura; Hitoshi Ozawa
Journal:  Med Mol Morphol       Date:  2012-12-07       Impact factor: 2.309

3.  Transcriptional Regulation of Human Transforming Growth Factor-α in Astrocytes.

Authors:  Pratap Karki; James Johnson; Deok-Soo Son; Michael Aschner; Eunsook Lee
Journal:  Mol Neurobiol       Date:  2016-01-21       Impact factor: 5.590

  3 in total

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