A proteomic analysis of murine bone marrow and its response to ionizing radiation

被引:33
作者
Chen, CW [1 ]
Lorimore, SA
Evans, CA
Whetton, AD
Wright, EG
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Dept Mol & Cellular Pathol, Dundee DD1 9SY, Scotland
[2] UMIST, Dept Biomol Sci, Manchester M60 1QD, Lancs, England
关键词
acute-phase response; bone marrow; ionizing radiation; proteomic analysis; tissue microenvironment;
D O I
10.1002/pmic.200401295
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To characterize the mouse bone marrow tissue proteome and investigate the response to radiation damage we took bone marrow before and after 4-Gy gamma-irradiation from mouse strains (C57BL/6 and CBA/Ca) that differ in their short-term and long-term radiation responses and analyzed extracellular proteins by high-resolution 2-DE. Twenty proteins were identified from 71 protein spots in both C57BL/6 and CBA/Ca. We detected significant differences between control and irradiated bone marrow and between genotypes and identified many of the changed proteins by MS. In C57BL/6, 27 spots were significantly different between control and irradiated samples. In CBA/Ca, 18 spots showed significant changes following irradiation. Proteins such as serum albumin, apolipoprotein A-I, ferritin, haptoglobin (Hp) and alpha-1-anfitrypsin were changed in irradiated bone marrow of both mouse strains, reflecting an ongoing acute-phase reaction. Several other proteins including serotransferrin, neutrophil collagenase, peroxiredoxin 2 and creatine kinase M chain were changed specifically in an individual mouse strain. The proteomic approach makes an important contribution to characterizing bone marrow proteome and investigating the tissue response of bone marrow to radiation, assists in identifying genotype-dependent responses and provides support for the importance of microenvironmental factors contributing to the overall response.
引用
收藏
页码:4254 / 4263
页数:10
相关论文
共 59 条
[1]   Toward a human blood serum proteome - Analysis by multidimensional separation coupled with mass spectrometry [J].
Adkins, JN ;
Varnum, SM ;
Auberry, KJ ;
Moore, RJ ;
Angell, NH ;
Smith, RD ;
Springer, DL ;
Pounds, JG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (12) :947-955
[2]  
[Anonymous], HUMAN CYTOKINES THEI
[3]   THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[4]   Current Issues in Mutagenesis and Carcinogenesis No. 98 - Radiation-induced genomic instability: a paradigm-breaking phenomenon and its relevance to environmentally induced cancer [J].
Baverstock, K .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2000, 454 (1-2) :89-109
[5]  
BLACKBURN WD, 1991, J LIPID RES, V32, P1911
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   Tissue-specific p53 responses to ionizing radiation and their genetic modification: the key to tissue-specific tumour susceptibility? [J].
Coates, PJ ;
Lorimore, SA ;
Lindsay, KJ ;
Wright, EG .
JOURNAL OF PATHOLOGY, 2003, 201 (03) :377-388
[8]  
ElGhmati SM, 1996, J IMMUNOL, V156, P2542
[9]  
Fajardo LF, 2001, RAD PATHOLOGY, P379
[10]   Induction of serum amyloid A inflammatory response genes in irradiated bone marrow cells [J].
Goltry, KL ;
Epperly, MW ;
Greenberger, JS .
RADIATION RESEARCH, 1998, 149 (06) :570-578