Cargando…

Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes

Electrophysiological and morphological methods were used to study connexin50 (Cx50) expressed in Xenopus laevis oocytes. Oocytes expressing Cx50 exhibited a new population of intramembrane particles (9.0 nm in diameter) in the plasma membrane. The particles represented hemichannels (connexin hexamer...

Descripción completa

Detalles Bibliográficos
Autores principales: Zampighi, Guido A., Loo, Donald D.F., Kreman, Michael, Eskandari, Sepehr, Wright, Ernest M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217170/
https://www.ncbi.nlm.nih.gov/pubmed/10102933
_version_ 1782149229044563968
author Zampighi, Guido A.
Loo, Donald D.F.
Kreman, Michael
Eskandari, Sepehr
Wright, Ernest M.
author_facet Zampighi, Guido A.
Loo, Donald D.F.
Kreman, Michael
Eskandari, Sepehr
Wright, Ernest M.
author_sort Zampighi, Guido A.
collection PubMed
description Electrophysiological and morphological methods were used to study connexin50 (Cx50) expressed in Xenopus laevis oocytes. Oocytes expressing Cx50 exhibited a new population of intramembrane particles (9.0 nm in diameter) in the plasma membrane. The particles represented hemichannels (connexin hexamers) because (a) their cross-sectional area could accommodate 24 ± 3 helices, (b) when their density reached 300–400/μm(2), they formed complete channels (dodecamers) in single oocytes, and assembled into plaques, and (c) their appearance in the plasma membrane was associated with a whole-cell current, which was activated at low external Ca(2+) concentration ([Ca(2+)](o)), and was blocked by octanol and by intracellular acidification. The Cx50 hemichannel density was directly proportional to the magnitude of the Cx50 Ca(2+)-sensitive current. Measurements of hemichannel density and the Ca(2+)-sensitive current in the same oocytes suggested that at physiological [Ca(2+)](o) (1–2 mM), hemichannels rarely open. In the cytoplasm, hemichannels were present in ∼0.1-μm diameter “coated” and in larger 0.2–0.5-μm diameter vesicles. The smaller coated vesicles contained endogenous plasma membrane proteins of the oocyte intermingled with 5–40 Cx50 hemichannels, and were observed to fuse with the plasma membrane. The larger vesicles, which contained Cx50 hemichannels, gap junction channels, and endogenous membrane proteins, originated from invaginations of the plasma membrane, as their lumen was labeled with the extracellular marker peroxidase. The insertion rate of hemichannels into the plasma membrane (80,000/s), suggested that an average of 4,000 small coated vesicles were inserted every second. However, insertion of hemichannels occurred at a constant plasma membrane area, indicating that insertion by vesicle exocytosis (60–500 μm(2) membranes/s) was balanced by plasma membrane endocytosis. These exocytotic and endocytotic rates suggest that the entire plasma membrane of the oocyte is replaced in ∼24 h.
format Text
id pubmed-2217170
institution National Center for Biotechnology Information
language English
publishDate 1999
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-22171702008-04-21 Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes Zampighi, Guido A. Loo, Donald D.F. Kreman, Michael Eskandari, Sepehr Wright, Ernest M. J Gen Physiol Article Electrophysiological and morphological methods were used to study connexin50 (Cx50) expressed in Xenopus laevis oocytes. Oocytes expressing Cx50 exhibited a new population of intramembrane particles (9.0 nm in diameter) in the plasma membrane. The particles represented hemichannels (connexin hexamers) because (a) their cross-sectional area could accommodate 24 ± 3 helices, (b) when their density reached 300–400/μm(2), they formed complete channels (dodecamers) in single oocytes, and assembled into plaques, and (c) their appearance in the plasma membrane was associated with a whole-cell current, which was activated at low external Ca(2+) concentration ([Ca(2+)](o)), and was blocked by octanol and by intracellular acidification. The Cx50 hemichannel density was directly proportional to the magnitude of the Cx50 Ca(2+)-sensitive current. Measurements of hemichannel density and the Ca(2+)-sensitive current in the same oocytes suggested that at physiological [Ca(2+)](o) (1–2 mM), hemichannels rarely open. In the cytoplasm, hemichannels were present in ∼0.1-μm diameter “coated” and in larger 0.2–0.5-μm diameter vesicles. The smaller coated vesicles contained endogenous plasma membrane proteins of the oocyte intermingled with 5–40 Cx50 hemichannels, and were observed to fuse with the plasma membrane. The larger vesicles, which contained Cx50 hemichannels, gap junction channels, and endogenous membrane proteins, originated from invaginations of the plasma membrane, as their lumen was labeled with the extracellular marker peroxidase. The insertion rate of hemichannels into the plasma membrane (80,000/s), suggested that an average of 4,000 small coated vesicles were inserted every second. However, insertion of hemichannels occurred at a constant plasma membrane area, indicating that insertion by vesicle exocytosis (60–500 μm(2) membranes/s) was balanced by plasma membrane endocytosis. These exocytotic and endocytotic rates suggest that the entire plasma membrane of the oocyte is replaced in ∼24 h. The Rockefeller University Press 1999-04-01 /pmc/articles/PMC2217170/ /pubmed/10102933 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Zampighi, Guido A.
Loo, Donald D.F.
Kreman, Michael
Eskandari, Sepehr
Wright, Ernest M.
Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes
title Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes
title_full Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes
title_fullStr Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes
title_full_unstemmed Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes
title_short Functional and Morphological Correlates of Connexin50 Expressed in Xenopus laevis Oocytes
title_sort functional and morphological correlates of connexin50 expressed in xenopus laevis oocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217170/
https://www.ncbi.nlm.nih.gov/pubmed/10102933
work_keys_str_mv AT zampighiguidoa functionalandmorphologicalcorrelatesofconnexin50expressedinxenopuslaevisoocytes
AT loodonalddf functionalandmorphologicalcorrelatesofconnexin50expressedinxenopuslaevisoocytes
AT kremanmichael functionalandmorphologicalcorrelatesofconnexin50expressedinxenopuslaevisoocytes
AT eskandarisepehr functionalandmorphologicalcorrelatesofconnexin50expressedinxenopuslaevisoocytes
AT wrighternestm functionalandmorphologicalcorrelatesofconnexin50expressedinxenopuslaevisoocytes