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Lens gap junctions in growth, differentiation, and homeostasis.
Mathias, Richard T; White, Thomas W; Gong, Xiaohua.
  • Mathias RT; Department of Physiology and Biophysics, SUNY at Stony Brook, Stony Brook, New York 11794-8661, USA. richard.mathias@stonybrook.edu
Physiol Rev ; 90(1): 179-206, 2010 Jan.
Article en En | MEDLINE | ID: mdl-20086076
ABSTRACT
The cells of most mammalian organs are connected by groups of cell-to-cell channels called gap junctions. Gap junction channels are made from the connexin (Cx) family of proteins. There are at least 20 isoforms of connexins, and most tissues express more than 1 isoform. The lens is no exception, as it expresses three isoforms Cx43, Cx46, and Cx50. A common role for all gap junctions, regardless of their Cx composition, is to provide a conduit for ion flow between cells, thus creating a syncytial tissue with regard to intracellular voltage and ion concentrations. Given this rather simple role of gap junctions, a persistent question has been Why are there so many Cx isoforms and why do tissues express more than one isoform? Recent studies of lens Cx knockout (KO) and knock in (KI) lenses have begun to answer these questions. To understand these roles, one must first understand the physiological requirements of the lens. We therefore first review the development and structure of the lens, its numerous transport systems, how these systems are integrated to generate the lens circulation, the roles of the circulation in lens homeostasis, and finally the roles of lens connexins in growth, development, and the lens circulation.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Uniones Comunicantes / Homeostasis / Cristalino Límite: Animals / Humans Idioma: En Año: 2010 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Uniones Comunicantes / Homeostasis / Cristalino Límite: Animals / Humans Idioma: En Año: 2010 Tipo del documento: Article