In:
Journal of Neurochemistry, Wiley, Vol. 109, No. 4 ( 2009-05), p. 1087-1095
Abstract:
In complex tissues where multiple subtypes of nicotinic acetylcholine receptors (nAChRs) are expressed, immunohistochemistry has been the most popular tool for investigation of nAChR subunit distribution. However, recent studies with nAChR subunit knockout mice demonstrated that a large panel of antibodies is unsuitable. Thus, we aimed to develop a histochemical method for selective labeling of α7 nAChR with neurotoxins, utilizing α7 nAChR‐transfected cells, dorsal root ganglia (DRG) and spinal cord from wild‐type and knockout mouse. The specificity of Alexa Fluor 488‐conjugated α‐bungarotoxin (Alexa‐αBgt) was demonstrated in binding to α7‐transfected cells inhibited by long‐chain α‐cobratoxin (CTX), but not short‐chain α‐neurotoxin II (NTII). In contrast, binding to Torpedo muscle‐type nAChRs and to motor end plates in mouse tongue sections was prevented by both CTX and NTII. In tissue sections of DRG, expressing all neuronal nAChR subunits, only CTX precluded Alexa‐αBgt labeling of neurons, with no staining for α7 nAChR knockout tissue. It proved that α7 nAChRs are the major αBgt‐binding sites in mouse DRG. Corresponding results were obtained for terminals in the spinal cord. Thus, we present a protocol utilizing Alexa‐αBgt and non‐labeled CTX/NTII that allows specific histochemical detection of α7 nAChR with a spatial resolution at the level of single axon terminals.
Type of Medium:
Online Resource
ISSN:
0022-3042
,
1471-4159
DOI:
10.1111/jnc.2009.109.issue-4
DOI:
10.1111/j.1471-4159.2009.06033.x
Language:
English
Publisher:
Wiley
Publication Date:
2009
detail.hit.zdb_id:
2020528-4
SSG:
12
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