Functional modules and expression of mouse p40phox and p67phox, SH3-domain-containing proteins -: Involved in the phagocyte NADPH oxidase complex

被引:68
作者
Mizuki, K
Kadomatsu, K
Hata, K
Ito, T
Fan, QW
Kage, Y
Fukumaki, Y
Sakaki, Y
Takeshige, K
Sumimoto, H
机构
[1] Kyushu Univ, Sch Med, Dept Biochem, Higashi Ku, Fukuoka 81282, Japan
[2] Nagoya Univ, Sch Med, Dept Biochem, Nagoya, Aichi, Japan
[3] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Tokyo, Japan
[4] Kyushu Univ, Inst Genet Informat, Fukuoka 812, Japan
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1998年 / 251卷 / 03期
关键词
NADPH oxidase; p67(phox); p40(phox); p47(phox); Src-homology-3; domain;
D O I
10.1046/j.1432-1327.1998.2510573.x
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 phagocyte NADPH oxidase is activated during phagocytosis to produce superoxide, a precursor of microbicidal oxidants. The formation of the active oxidase complex at the membrane requires translocation of the Rac GTPase and two specialized cytosolic proteins that harbor SH3 domains, p67(phox) and p47(phox). Another SH3-domain-containing protein p40(phox), which is constitutively associated with p67(phox) in phagocytes, also enters the complex upon cell stimulation. Here we describe how we cloned mouse cDNAs encoding p40(phox) and its partner in phagocytes, p67(phox). Both p40(phox) and p67(phox) comprise several protein-binding modules that are structurally and functional well conserved between mouse and human, indicating their nature as adaptor proteins. We have also systematically investigated expression of the gene for p40(phox) in comparison with those for p67(phox) and p47(phox). Distributions of the mRNAs for the three proteins among tissues are similar, with the most abundant: expression in the spleen. The messages are abundant not only in phagocytic cells, but also in B cell lineage. The p40(phox) gene, but not the other two, is expressed in some types of cells such as plasma cells and T lymphocytes, Furthermore, in situ hybridization analysis shows that the p40(phox) mRNA is distributed in neuronal cells of mouse brain, providing evidence that one of the genes for the specialized oxidase factors is expressed in neurons. These observations raise the possibility that the adaptor protein p40(phox) plays a heretofore unsuspected role via interacting with other proteins in the cells that do not express p67(phox)or p47(phox).
引用
收藏
页码:573 / 582
页数:10
相关论文
共 44 条
[21]   INTERACTIONS BETWEEN THE CYTOSOLIC COMPONENTS P47(PHOX) AND P67(PHOX) OF THE HUMAN NEUTROPHIL NADPH OXIDASE THAT ARE NOT REQUIRED FOR ACTIVATION IN THE CELL-FREE SYSTEM [J].
LEUSEN, JHW ;
FLUITER, K ;
HILARIUS, PM ;
ROOS, D ;
VERHOEVEN, AJ ;
BOLSCHER, BGJM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (19) :11216-11221
[22]   STRUCTURAL DETERMINANTS OF PEPTIDE-BINDING ORIENTATION AND OF SEQUENCE SPECIFICITY IN SH3 DOMAINS [J].
LIM, WA ;
RICHARDS, FM ;
FOX, RO .
NATURE, 1994, 372 (6504) :375-379
[23]  
MAEDA K, 1988, J IMMUNOL, V140, P2796
[24]   SH3-DEPENDENT ASSEMBLY OF THE PHAGOCYTE NADPH OXIDASE [J].
MCPHAIL, LC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) :2011-2015
[25]   The PC motif:: a novel and evolutionarily conserved sequence involved in interaction between p40phox and p67phox, SH3 domain-containing cytosolic factors of the phagocyte NADPH oxidase [J].
Nakamura, R ;
Sumimoto, H ;
Mizuki, K ;
Hata, K ;
Ago, T ;
Kitajima, S ;
Takeshige, K ;
Sakaki, Y ;
Ito, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 251 (03) :583-589
[26]   PROTEIN MODULES AND SIGNALING NETWORKS [J].
PAWSON, T .
NATURE, 1995, 373 (6515) :573-580
[27]   CHARACTERIZATION OF THE 47-KILODALTON AUTOSOMAL CHRONIC GRANULOMATOUS-DISEASE PROTEIN - TISSUE-SPECIFIC EXPRESSION AND TRANSCRIPTIONAL CONTROL BY RETINOIC ACID [J].
RODAWAY, ARF ;
TEAHAN, CG ;
CASIMIR, CM ;
SEGAL, AW ;
BENTLEY, DL .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5388-5396
[28]  
Roos D, 1996, BLOOD, V87, P1663
[29]  
Sathyamoorthy M, 1997, J BIOL CHEM, V272, P9141
[30]  
SMITH RM, 1991, BLOOD, V77, P673