Tumour necrosis factor α alters the expression of connexin43, connexin40, and connexin37 in human umbilical vein endothelial cells

被引:119
作者
van Rijen, HVM
van Kempen, MJA
Postma, S
Jongsma, HJ
机构
[1] Univ Utrecht, Fac Med, Dept Med Physiol & Sports Med, NL-3584 CG Utrecht, Netherlands
[2] Univ Amsterdam, Fac Med, Dept Physiol, NL-1105 AZ Amsterdam, Netherlands
关键词
cytokine; gap junctions; immunohistochemistry; RT-PCR;
D O I
10.1006/cyto.1997.0287
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
Tumour necrosis factor alpha (TNF-alpha) plays an important role in orchestrating inflammatory responses with the vascular endothelium as main target cell type, and was found to promote migration of endothelial cells, as occurs in wound healing processes, Substantial evidence exists that endothelial cell migration in wound healing is related to changes in cell coupling by means of gap junctions. Gap junctions are agglomerates of cell-to-cell channels that allow direct electrical and metabolic communication between cells. The authors have investigated whether TNF-alpha alters the expression of gap junction proteins (connexins, Cx) between human umbilical vein endothelial cells (HUVEC), thereby changing the extent of intercellular communication, as measured by dye coupling. Under control conditions, Cx43, Cx40, and Cx37 protein and mRNA were present in HUVEC, After exposure to 0.5 nM TNF-alpha for 48 h, however, the authors were no longer able to detect Cx37 and Cx40 protein, whereas Cx43 levels seemed unaltered but showed more perinuclear staining. After 24 and 48 h exposure to TNF-alpha, levels of Cx37 and Cx40 mRNA, were reduced, while the level of Cx43 mRNA remained unaltered, suggesting transcriptional regulation. If TNF-alpha was removed from the medium, Cx37 and Cx40 expression was restored within 24 h, The modulation of connexin expression by TNF-alpha resulted in a decrease in dye coupling of 40%. (C) 1998 Academic Press Limited.
引用
收藏
页码:258 / 264
页数:7
相关论文
共 39 条
[31]   COUPLING AND CONNEXIN-43 EXPRESSION IN MICROVASCULAR AND LARGE VESSEL ENDOTHELIAL-CELLS [J].
PEPPER, MS ;
MONTESANO, R ;
ELAOUMARI, A ;
GROS, D ;
ORCI, L ;
MEDA, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (05) :C1246-C1257
[32]   CYTOKINES AND ENDOTHELIAL-CELL BIOLOGY [J].
POBER, JS ;
COTRAN, RS .
PHYSIOLOGICAL REVIEWS, 1990, 70 (02) :427-451
[33]   PHOSPHORYLATION OF THE SMALL HEAT-SHOCK PROTEIN IS REGULATED BY INTERLEUKIN-1, TUMOR-NECROSIS-FACTOR, GROWTH-FACTORS, BRADYKININ AND ATP [J].
SAKLATVALA, J ;
KAUR, P ;
GUESDON, F .
BIOCHEMICAL JOURNAL, 1991, 277 :635-642
[34]  
SATO N, 1986, JNCI-J NATL CANCER I, V76, P1113
[35]   IMMUNOELECTRON MICROSCOPIC LOCALIZATION OF TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR ON THE SURFACE OF ACTIVATED ENDOTHELIAL-CELLS [J].
SCHLEEF, RR ;
LOSKUTOFF, DJ ;
PODOR, TJ .
JOURNAL OF CELL BIOLOGY, 1991, 113 (06) :1413-1423
[36]   TRAFFIC SIGNALS FOR LYMPHOCYTE RECIRCULATION AND LEUKOCYTE EMIGRATION - THE MULTISTEP PARADIGM [J].
SPRINGER, TA .
CELL, 1994, 76 (02) :301-314
[37]  
STOLPEN AH, 1986, AM J PATHOL, V123, P16
[38]   Gap junctions in human umbilical cord endothelial cells contain multiple connexins [J].
vanRijen, HVM ;
vanKempen, MJA ;
Analbers, LJS ;
Rook, MB ;
vanGinneken, ACG ;
Gros, D ;
Jongsma, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (01) :C117-C130
[39]  
VANRIJEN HVM, 1997, THESIS U AMSTERDAM A