E-NTPase/NTPDase: potential role as a regulatory element in inflammation

被引:13
作者
Kannan, S [1 ]
机构
[1] Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
关键词
D O I
10.1054/mehy.2001.1509
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Inflammation is a process culminated by cellular components and soluble mediators act in concert to evolve a sustainable process to impart distress in vascularized tissue. Among the contributors, extracellular nucleotides are prominent in PMN granule release (degranulation); chemotaxis, enhanced expression of adhesion molecule on the surface of PMN. However, co-stimulatory effectors such as chemokines are required for the extracellular nucleotide-induced maximal effect in inflammation. Enzymes, which degrade the extracellular nucleotide(s), could potentially attenuate or minimize the extracellular nucleotide(s) induced effect by degradation. (C) 2002 Published by Elsevier Science Ltd.
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页码:527 / 528
页数:2
相关论文
共 21 条
[1]  
BALAZOVICH KJ, 1990, J IMMUNOL, V144, P631
[2]   HYPOXIA, ENDOTHELIUM, AND PURINES [J].
BURNSTOCK, G .
DRUG DEVELOPMENT RESEARCH, 1993, 28 (03) :301-305
[3]   ATP STIMULATES SECRETION IN HUMAN-NEUTROPHILS AND HL60 CELLS VIA A PERTUSSIS TOXIN-SENSITIVE GUANINE NUCLEOTIDE-BINDING PROTEIN COUPLED TO PHOSPHOLIPASE-C [J].
COCKCROFT, S ;
STUTCHFIELD, J .
FEBS LETTERS, 1989, 245 (1-2) :25-29
[4]   SIGNAL-TRANSDUCTION VIA P2-PURINERGIC RECEPTORS FOR EXTRACELLULAR ATP AND OTHER NUCLEOTIDES [J].
DUBYAK, GR ;
ELMOATASSIM, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (03) :C577-C606
[5]   EXTRACELLULAR ATP STIMULATES ELASTASE SECRETION FROM HUMAN NEUTROPHILS AND INCREASES LUNG RESISTANCE AND SECRETION FROM NORMAL RAT AIRWAYS AFTER INTRATRACHEAL INSTILLATION [J].
FLEZAR, M ;
OLIVENSTEIN, R ;
CANTIN, A ;
HEISLER, S .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1992, 70 (07) :1065-1068
[6]   Caregiving and employment: The impact of workplace characteristics on role strain [J].
Fredriksen, KI ;
Scharlach, AE .
JOURNAL OF GERONTOLOGICAL SOCIAL WORK, 1997, 28 (04) :3-22
[7]   Inhibition of platelet function by recombinant soluble ecto-ADPase/CD39 [J].
Gayle, RB ;
Maliszewski, CR ;
Gimpel, SD ;
Schoenborn, MA ;
Caspary, RG ;
Richards, C ;
Brasel, K ;
Price, V ;
Drosopoulos, JHF ;
Islam, N ;
Alyonycheva, TN ;
Broekman, MJ ;
Marcus, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (09) :1851-1859
[8]   EXTRACELLULAR ATP - EFFECTS, SOURCES AND FATE [J].
GORDON, JL .
BIOCHEMICAL JOURNAL, 1986, 233 (02) :309-319
[9]  
HUTCHINSON AWF, 1994, CANC METASTASIS REV, V3, P257
[10]   Identification and characterization of CD39 vascular ATP diphosphohydrolase [J].
Kaczmarek, E ;
Koziak, K ;
Sevigny, J ;
Siegel, JB ;
Anrather, J ;
Beaudoin, AR ;
Bach, FH ;
Robson, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (51) :33116-33122