A quantitative immunocytochemical study of a G-protein-gated inward rectifier potassium channel (GIRK2) in the weaver mice mesencephalon.

ADELBRECHT C; MURER MG; LAURITZEN I; LESAGE F; LAZDUNSKI M; AGID Y; RAISMAN-VOZARI R

NEUROREPORT

LIPPINCOTT WILLIAMS & WILKINS

Lugar: Philadelphia; Año: 1997 vol. 8 p. 979 - 984

0959-4965

It has been suggested that a mutation in a G-protein-gated inward rectifier K+ channel (GIRK2) is responsible for inducing cell death in the cerebellum of homozygous weaver (wv/wv) mutant mice. These mice also display a progressive, massive loss of mesencephalic dopaminergic neurones. Using an immunocytochemical method, we detected GIRK2-positive cell bodies and fibres in the substantia nigra pars compacta (SNC) and the ventral tegmental area (VTA) of control (+/+) mice. Cell counts of both GIRK2- and tyrosine hydroxylase (TH)-positive neurones demonstrated a marked loss of SNC cell bodies, especially in 12-month-old (12M) wv/wv mice. A considerable proportion of GIRK2-positive cell bodies were preserved, however. In addition, no loss of GIRK2-positive neurones was observed in the VTA of 12M wv/wv mice, despite of a significant reduction in TH-positive cell bodies. These results suggest that expression of the mutated channel is not a sufficient condition to induce cell death in the ventral mesencephalon of the wv/wv mice.