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Canlon B, Homburger V, Bockaert J. The Identification and Localization of the Guanine Nucleotide Binding Protein G0 in the Auditory System. Eur J Neurosci. 1991;3(12):1338-1342doi: 10.1111/j.1460-9568.1991.tb00066.x.
Canlon, B., Homburger, V., & Bockaert, J. (1991). The Identification and Localization of the Guanine Nucleotide Binding Protein G0 in the Auditory System. The European journal of neuroscience, 3(12), 1338-1342. https://doi.org/10.1111/j.1460-9568.1991.tb00066.x
Canlon, Barbara, et al. "The Identification and Localization of the Guanine Nucleotide Binding Protein G0 in the Auditory System." The European journal of neuroscience vol. 3,12 (1991): 1338-1342. doi: https://doi.org/10.1111/j.1460-9568.1991.tb00066.x
Canlon B, Homburger V, Bockaert J. The Identification and Localization of the Guanine Nucleotide Binding Protein G0 in the Auditory System. Eur J Neurosci. 1991;3(12):1338-1342. doi: 10.1111/j.1460-9568.1991.tb00066.x. PMID: 12106231.
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Eur J Neurosci. 1991;3(12):1338-1342. doi: 10.1111/j.1460-9568.1991.tb00066.x.

The Identification and Localization of the Guanine Nucleotide Binding Protein G0 in the Auditory System.

The European journal of neuroscience

Barbara Canlon, Vincent Homburger, Joël Bockaert

Affiliations

  1. Department of Physiology II, Karolinska Institutet, S-10401 Stockholm, Sweden.

PMID: 12106231 DOI: 10.1111/j.1460-9568.1991.tb00066.x

Abstract

The identification of guanine nucleotide binding proteins (G proteins) in guinea-pig tissues was assessed by the adenosine diphosphate-ribosylation of the alpha subunit by Bordetella pertussis toxin using [alpha32P]nicotinamide adenine dinucleotide as the substrate followed by sodium dodecyl sulphate - polyacrylamide gel electrophoresis and autoradiography. Three tissues (inferior colliculus, neuroblastoma cells, and the organ of Corti) contained G0alpha (39 kD), as well as Gi2alpha (40 kD) and Gi1alpha and/or Gi3alpha (41 kD). The stria vascularis and the VIIIth nerve contained mainly Gi2alpha, Gi1alpha and/or Gi3alpha, but G0alpha was barely detectable. A purified preparation of outer hair cells from the organ of Corti contained all three pertussis toxin substrates including G0alpha, with the Gi2alpha (40 kD) subunit being the most prominent. The immunocytochemical localization of the G0alpha subunit was determined by light microscopy after incubating isolated outer hair cells, Hensen cells and the stria vascularis with affinity-purified anti-G0alpha antibodies. In hair cells a positive reaction was observed along the plasma membrane and around the perimeter of the cuticular plate (zona adherens). Positive reaction was also observed within the infracuticular network extending from the cuticular plate towards the nucleus in outer hair cells. Finally, the base of the outer hair cells also contained G0alpha. However, it is likely that the G0alpha that is present in this cell region is not within the hair cell itself, but rather in nerve terminals which remained attached during dissection.

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