CELLULAR-DISTRIBUTION OF NICOTINIC ACETYLCHOLINE-RECEPTOR SUBUNIT MESSENGER-RNAS IN THE HUMAN CEREBRAL-CORTEX AS REVEALED BY NONISOTOPIC IN-SITU HYBRIDIZATION
A. Wevers et al., CELLULAR-DISTRIBUTION OF NICOTINIC ACETYLCHOLINE-RECEPTOR SUBUNIT MESSENGER-RNAS IN THE HUMAN CEREBRAL-CORTEX AS REVEALED BY NONISOTOPIC IN-SITU HYBRIDIZATION, Molecular brain research, 25(1-2), 1994, pp. 122-128
The pharmacology of telencephalic nicotinic acetylcholine receptors (n
AChRs) has become an important issue in recent years. While in the hum
an brain a direct pharmacological assessment is difficult to achieve t
he visualization of nAChRs has been enabled by histochemical technique
s providing an ever increasing and improving resolution. Receptor auto
radiography was used to visualize binding sites on the level of cortic
al layers whereas immunohistochemistry has allowed for the cell type-s
pecific and ultrastructural localization of receptor protein. Further
investigations have to elucidate the cellular sites of nAChR biosynthe
sis by visualizing subunit-specific transcripts. Using autopsy samples
of the human precentral cortex (Area 4) as a paradigm we have applied
digoxigenin-labeled cRNA probes to localize transcripts for the alpha
3- and alpha 4-1-subunits of the nAChR. In accordance with findings i
n the monkey cortex, the alpha 3-subunit seems to be expressed mainly
in pyramidal neurons of layers III-VI of the human cerebral cortex. Tr
anscripts for the alpha 4-1-subunit, by contrast, appear to be present
in a large number of neurons throughout all layers of the cerebral co
rtex, consonant with its ubiquitous distribution in the rodent brain.
The present findings show that also in human autopsy brains the cell t
ype-specific detection of nAChR transcripts is possible. For the futur
e, this technique will enable to investigate the expression of recepto
r transcripts in diseased human brains as compared to controls.