Array analysis of gene expression in connexin-43 null astrocytes

被引:90
作者
Iacobas, DA [1 ]
Maldonado, MU [1 ]
Iacobas, S [1 ]
Scemes, E [1 ]
Spray, DC [1 ]
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
关键词
glia; gap junction; knockout; DNA array; intercellular communication;
D O I
10.1152/physiolgenomics.00062.2003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Connexin-43 (Cx43) is the most abundant gap junction protein in brain, where it is found primarily between astrocytes. Although the morphology of astrocytes from Cx43-null (knockout, KO) mice is similar to that of wild-type (WT) astrocytes, KO astrocytes exhibit reduced growth rate in culture. To evaluate the impact of deletion of Cx43 on other genes, including those encoding cell cycle proteins, we used DNA arrays to determine expression patterns in cultured astrocytes from sibling Cx43-null and WT mice. RNA samples extracted from astrocytes cultured from WT and Cx43-null neonatal mice were dye labeled and individually cohybridized with a reference of labeled cDNAs pooled from a variety of tissues on 8 gene arrays containing 8,975 mouse DNA sequences. Normal variability in expression of each gene was evaluated and incorporated into "expression scores" to statistically compare expression levels between WT and KO samples. In Cx43-null astrocytes, 4.1% of the 4,998 adequately quantifiable spots were found to have significantly (P < 0.05) decreased hybridization compared with controls, and 9.4% of the spots showed significantly higher hybridization. The significantly different spots corresponded to RNAs encoding 252 known proteins, many not previously linked to gap junctions, including transcription factors, channels and transporters, cell growth and death signals, enzymes and cell adhesion molecules. These data indicate a surprisingly high degree of impact of deletion of Cx43 on other astrocyte genes, implying that gap junction gene expression alters numerous processes in addition to intercellular communication.
引用
收藏
页码:177 / 190
页数:14
相关论文
共 61 条
[41]   Myocardial architecture and ventricular arrhythmogenesis [J].
Peters, NS ;
Wit, AL .
CIRCULATION, 1998, 97 (17) :1746-1754
[42]   Transduction of cell survival signals by connexin-43 hemichannels [J].
Plotkin, LI ;
Manolagas, SC ;
Bellido, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8648-8657
[43]   Retroviral delivery of connexin genes to human breast tumor cells inhibits in vivo tumor growth by a mechanism that is independent of significant gap junctional intercellular communication [J].
Qin, H ;
Shao, Q ;
Curtis, H ;
Galipeau, J ;
Belliveau, DJ ;
Wang, TQ ;
Alaoui-Jamali, MA ;
Laird, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (32) :29132-29138
[44]   Cell-specific expression of connexins and evidence of restricted gap junctional coupling between glial cells and between neurons [J].
Rash, JE ;
Yasumura, T ;
Dudek, FE ;
Nagy, JI .
JOURNAL OF NEUROSCIENCE, 2001, 21 (06) :1983-2000
[45]   CARDIAC MALFORMATION IN NEONATAL MICE LACKING CONNEXIN43 [J].
REAUME, AG ;
DESOUSA, PA ;
KULKARNI, S ;
LANGILLE, BL ;
ZHU, DG ;
DAVIES, TC ;
JUNEJA, SC ;
KIDDER, GM ;
ROSSANT, J .
SCIENCE, 1995, 267 (5205) :1831-1834
[46]  
Rozental R, 1998, J NEUROSCI, V18, P1753
[47]   Temporal expression of neuronal connexins during hippocampal ontogeny [J].
Rozental, R ;
Srinivas, M ;
Gökhan, S ;
Urban, M ;
Dermietzel, R ;
Kessler, JA ;
Spray, DC ;
Mehler, MF .
BRAIN RESEARCH REVIEWS, 2000, 32 (01) :57-71
[48]  
Scemes E, 2000, J NEUROSCI, V20, P1435
[49]  
SPLITT MP, 1995, NEW ENGL J MED, V333, P941
[50]  
Spray DC, 1999, ADV EXP MED BIOL, V468, P339