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The regulation of proenkephalin expression in a distinct population of glial cells.
Author(s) -
Melner M.H.,
Low K.G.,
Allen R.G.,
Nielsen C.P.,
Young S.L.,
Saneto R.P.
Publication year - 1990
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1002/j.1460-2075.1990.tb08175.x
Subject(s) - biology , primate , population , research center , library science , evolutionary biology , neuroscience , demography , sociology , political science , computer science , law
The expression of opioid genes was examined in isolated populations of glial cells in primary culture. Northern blot analysis of purified type I astrocytes, oligodendrocytes and mixed oligodendrocyte‐type‐2‐astrocyte lineage cells derived from cerebral cortex demonstrated robust expression of proenkephalin mRNA exclusively in type I astrocytes. The expression of proenkephalin mRNA was stimulated by the beta‐adrenergic agonist isoproterenol, and 8‐(4‐chlorophenyl thio)adenosine 3′‐5′‐cyclic monophosphate (cpt‐cAMP). Both of these compounds regulated a proenkephalin‐chloramphenicol acetyltransferase fusion gene transiently transfected into type I astrocytes. HPLC and immunoassay of the cell culture media revealed significant levels of unprocessed proenkephalin secreted by the cell and this secretion was stimulated by isoproterenol and cpt‐cAMP. The relatively high levels of proenkephalin expressed suggest that enhanced expression in astrocytes may be important during neural development, in trauma‐induced gliosis and in neuroimmune interactions.