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Hormonal Regulation of the mRNA Encoding the Ketogenic Enzyme Mitochondrial 3‐Hydroxy‐3‐Methylglutaryl‐CoA Synthase in Neonatal Primary Cultures of Cortical Astrocytes and Meningeal Fibroblasts
Author(s) -
Cullingford Tim E.,
Bhakoo Kishore K.,
Clark John B.
Publication year - 1998
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1998.71051804.x
Subject(s) - biology , endocrinology , cerebellum , thiolase , medicine , messenger rna , hormone , glucocorticoid , enzyme , biochemistry , dehydrogenase , gene
We have previously identified cerebellum to contain significantly higher levels, compared with other brain regions, of the mRNA encoding the key ketogenic enzyme mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase (mHS). In this report, we extend these observations, using primary cultures of cerebellar astrocytes and cerebellar granule neurons, and show that mHS mRNA was not readily detected in these cell types, suggesting that other cerebellar cell types account for mHS mRNA abundances observed in cerebellum. In contrast, we report, for the first time, the ready detection of mHS mRNA together with the mRNAs encoding the remaining enzymes of the 3‐hydroxy‐3‐methylglutaryl‐CoA cycle, namely, mitochondrial acetoacetyl‐CoA thiolase and 3‐hydroxy‐3‐methylglutaryl‐CoA lyase, in primary cultures of neonatal meningeal fibroblasts. Based on observations of the effects of fetal calf serum in the culture medium and the documented effects of various hormones on mHS mRNA levels in liver, we show that the glucocorticoid hydrocortisone effects a selective fourfold increase in mHS mRNA abundances in both neonatal meningeal fibroblasts and neonatal cortical astrocytes cultured in a serum‐free/hormone‐free medium.