Microarray analysis of fiber cell maturation in the lens

被引:32
作者
Ivanov, D
Dvoriantehikova, G
Pestova, A
Nathanson, L
Shestopalova, VI
机构
[1] Univ Miami, Miller Sch Med, Dept Ophthalmol, Bascom Palmer Eye Inst, Miami, FL 33136 USA
[2] RAS, Vavilov Inst Gen Genet, Moscow, Russia
[3] Univ Miami, Miller Sch Med, Dept Mol & Cellular Pharmacol, Miami, FL USA
[4] Univ Miami, Miller Sch Med, Dept Cell Biol & Anat, Miami, FL USA
来源
FEBS LETTERS | 2005年 / 579卷 / 05期
关键词
lens; differentiation; microarray; gene expression profiling; laser capture microdissection; RNA amplification;
D O I
10.1016/j.febslet.2005.01.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian lens consists of an aged core of quiescent cells enveloped by layers of mature fully elongated cells and younger, continuously elongating transcriptionally active cells. The fiber cell maturation is initiated when fiber cells cease to elongate. The process of maturation represents a radical switch from active elongation to a life-long quiescence and has not been studied previously. It may also include critical stages of preparation for the organelle removal and denucleation. In the present study, we used laser capture microdisection (LCM) microdissection and RNA amplification to compare global gene expression profiles of young elongating and mature, non-elongating fiber cells. Analysis of microarray data from three independent dye-swap experiments identified 65 differentially expressed genes (FDR < 0.1) with greater than 2-fold change in expression levels. Microarray array results for a group of randomly selected genes were confirmed by quantitative RT-PCR. These microarray results provide clues to understanding the molecular pathways underlying lens development. The identified changes in the profile of gene expression reflected a shift in cell physiology characterizing the lens fiber maturation. (C) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1213 / 1219
页数:7
相关论文
共 51 条
[1]   Isolation of Bcl-2 binding proteins that exhibit homology with BAG-1 and suppressor of death domains protein [J].
Antoku, K ;
Maser, RS ;
Scully, WJ ;
Delach, SM ;
Johnson, DE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (05) :1003-1010
[2]  
Bassnett S, 1997, INVEST OPHTH VIS SCI, V38, P1678
[3]   Chromatin degradation in differentiating fiber cells of the eye lens [J].
Bassnett, S ;
Mataic, D .
JOURNAL OF CELL BIOLOGY, 1997, 137 (01) :37-49
[4]   Lens organelle degradation [J].
Bassnett, S .
EXPERIMENTAL EYE RESEARCH, 2002, 74 (01) :1-6
[5]   COINCIDENT LOSS OF MITOCHONDRIA AND NUCLEI DURING LENS FIBER CELL-DIFFERENTIATION [J].
BASSNETT, S ;
BEEBE, DC .
DEVELOPMENTAL DYNAMICS, 1992, 194 (02) :85-93
[6]  
BASSNETT S, 1990, INVEST OPHTH VIS SCI, V31, P1637
[7]  
BASSNETT S, 2004, DEV OCULAR LENS LOVI
[8]   Quantitative analysis of mRNA amplification by in vitro transcription [J].
Baugh, L. R. ;
Hill, A. A. ;
Brown, E. L. ;
Hunter, Craig P. .
NUCLEIC ACIDS RESEARCH, 2001, 29 (05)
[9]   THE MECHANISM OF CELL ELONGATION DURING LENS FIBER CELL-DIFFERENTIATION [J].
BEEBE, DC ;
COMPART, PJ ;
JOHNSON, MC ;
FEAGANS, DE ;
FEINBERG, RN .
DEVELOPMENTAL BIOLOGY, 1982, 92 (01) :54-59
[10]   VOLUME REGULATION IN LENS EPITHELIAL-CELLS AND DIFFERENTIATING LENS FIBER CELLS [J].
BEEBE, DC ;
PARMELEE, JT ;
BELCHER, KS .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (03) :455-459