Structural and immunocytochemical alterations in eye lens fiber cells from Cx46 and Cx50 knockout mice

被引:27
作者
Dunia, Irene
Cibert, Christian
Gong, Xiaohua
Xia, Chun-hong
Recouvreur, Michel
Levy, Essy
Kumar, Nalin
Bloemendal, Hans
Benedetti, E. Lucio
机构
[1] Univ Paris 06, CNRS, Inst Jacques Monod, F-75251 Paris 5, France
[2] Univ Calif Berkeley, Sch Optometry, Berkeley, CA 94720 USA
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[4] Univ Illinois, Dept Ophthalmol & Visual Sci, Chicago, IL 60612 USA
[5] Radboud Univ Nijmegen, Dept Biochem, Nijmegen, Netherlands
关键词
gap junction; morphometry; fracture-labeling; MP26; aquaporin; 0; connexin; 46; 50; cataract;
D O I
10.1016/j.ejcb.2006.03.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the current study we describe the changes of overall organization of lens fiber cells in connexin 46 (Cx46) and connexin 50 (Cx50) knockout mice. Morphometric analyses and the application of immunocytochemical techniques revealed that in Cx46 knockout lens (Cx46 -/-), where Cx50 is expressed alone, the postnatal differentiation of secondary fiber cells proceeds faster and is characterized by an increased number of smaller fiber cells. Conversely, in Cx50 knockout mice (Cx50 -/-), the lenticular mass is considerably reduced and characterized by a small number of fiber cells added during the postnatal period. The process of terminal differentiation was impaired and generated larger fiber cells still possessing cytoplasmic organelles. Freeze-fracture and fracture labeling revealed that the Junctional assembly, packing organization and topographic interactions between connexons and MP26 differed when Cx46 and Cx50 were co-assembled in the wild-type or expressed separately in the two distinct knockout phenotypes. Filipin cytochemistry provided indirect evidence that Cx46 and Cx50 expressed alone are recruited into different lipid environments. Our results represent the structural proof that interaction of connexins and MP26 contributes to the overall organization of the fiber cells. (c) 2006 Elsevier GmbH. All rights reserved.
引用
收藏
页码:729 / 752
页数:24
相关论文
共 91 条
[41]   Properties of gap junction channels formed by Cx46 alone and in combination with Cx50 [J].
Hopperstad, MG ;
Srinivas, M ;
Spray, DC .
BIOPHYSICAL JOURNAL, 2000, 79 (04) :1954-1966
[42]  
HYATT GA, 1993, DEVELOPMENT, V117, P701
[43]   Gap junction processing and redistribution revealed by quantitative optical measurements of connexin46 epitopes in the lens [J].
Jacobs, MD ;
Soeller, C ;
Sisley, AMG ;
Cannell, MB ;
Donaldson, P .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 (01) :191-199
[44]   Quantifying changes in gap junction structure as a function of lens fiber cell differentiation [J].
Jacobs, MD ;
Soeller, C ;
Cannell, MB ;
Donaldson, PJ .
CELL COMMUNICATION AND ADHESION, 2001, 8 (4-6) :349-+
[45]  
JAHNE B, 1993, DIGITAL IMAGE PROCES
[46]   Heteromeric connexons in lens gap junction channels [J].
Jiang, JX ;
Goodenough, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1287-1291
[47]   Regulation of lens fiber cell differentiation by transcription factor c-Maf [J].
Kawauchi, S ;
Takahashi, S ;
Nakajima, O ;
Ogino, H ;
Morita, M ;
Nishizawa, M ;
Yasuda, K ;
Yamamoto, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :19254-19260
[48]   MOLECULAR PORTRAIT OF LENS GAP JUNCTION PROTEIN MP70 [J].
KISTLER, J ;
BERRIMAN, J ;
EVANS, CW ;
GRUIJTERS, WTM ;
CHRISTIE, D ;
CORIN, A ;
BULLIVANT, S .
JOURNAL OF STRUCTURAL BIOLOGY, 1990, 103 (03) :204-211
[49]   2 DISTINCT LEVELS OF GAP JUNCTION ASSEMBLY INVITRO [J].
KISTLER, J ;
BOND, J ;
DONALDSON, P ;
ENGEL, A .
JOURNAL OF STRUCTURAL BIOLOGY, 1993, 110 (01) :28-38
[50]   RECONSTITUTION OF NATIVE-TYPE NONCRYSTALLINE LENS FIBER GAP-JUNCTIONS FROM ISOLATED HEMICHANNELS [J].
KISTLER, J ;
GOLDIE, K ;
DONALDSON, P ;
ENGEL, A .
JOURNAL OF CELL BIOLOGY, 1994, 126 (04) :1047-1058