MUC1 in normal and impaired spermatogenesis

被引:21
作者
Franke, FE
Kraus, S
Eiermann, C
Pauls, K
Lalani, EN
Bergmann, M
机构
[1] Univ Giessen, Dept Pathol, D-35392 Giessen, Germany
[2] Univ Giessen, Dept Urol, D-35392 Giessen, Germany
[3] Univ Giessen, Dept Vet Anat, D-35392 Giessen, Germany
[4] Univ London Imperial Coll Sci Technol & Med, Dept Histopathol, London, England
关键词
immunohistochemistry; MUC1; mucins; RT/PCR; RT-PCR; spermatogenesis;
D O I
10.1093/molehr/7.6.505
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The MUC1 mucin [also known as episialin, epithelial membrane antigen (EMA) or polymorphic epithelial mucin (PEM)] is a component of the mucosal glycocalyx, contributing to anti-adhesive and protective cell functions. MUC1 has been shown in a variety of epithelial cell types in the reproductive tracts of males and females, but this is the first report of its expression in human testis and non-epithelial cells of the germ cell lineage. Analysing 65 testes with normal or impaired spermatogenesis, we identified MUC1 protein in maturing germ cells by immunohistochemistry using the monoclonal antibodies HMFG1, HMFG2 and SM3 binding to different glycosylation variants. MUC1 expression was confirmed by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot analysis on tissue extracts of human testis, and RT-PCR of selected germ cells after UV laser-assisted cell picking. MUC1 glycosylation variants were selectively distributed during normal spermatogenesis, Whereas HMFG1 labelled certain groups of pachytene spermatocytes, HMFG2 labelled only spermatids, Low glycosylated forms of MUC1 mucin, recognized by SM3, were not found. In contrast to its weak expression during normal spermatogenesis, the HMFG1 glycosylation variant accumulated markedly in all spermatocytes showing abnormal or arrested maturation, These results suggest a variable glycosylation of MUC1 mucin in differentiating germ cells, which is aberrant in pathological conditions.
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页码:505 / 512
页数:8
相关论文
共 36 条
[1]  
Baruch A, 1999, CANCER RES, V59, P1552
[2]   Cloning of a human UDP-N-acetyl-α-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase that complements other GalNAc-transferases in complete O-glycosylation of the MUC1 tandem repeat [J].
Bennett, EP ;
Hassan, H ;
Mandel, U ;
Mirgorodskaya, E ;
Roepstorff, P ;
Burchell, J ;
Taylor-Papadimitriou, J ;
Hollingsworth, MA ;
Merkx, G ;
van Kessel, AG ;
Eiberg, H ;
Steffensen, R ;
Clausen, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30472-30481
[3]   THE PRODUCT OF THE HUMAN MUC1 GENE WHEN SECRETED BY MOUSE CELLS TRANSFECTED WITH THE FULL-LENGTH CDNA LACKS THE CYTOPLASMIC TAIL [J].
BOSHELL, M ;
LALANI, EN ;
PEMBERTON, L ;
BURCHELL, J ;
GENDLER, S ;
TAYLORPAPADIMITRIOU, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 185 (01) :1-8
[4]  
BURCHELL J, 1993, EPITHELIAL CELL BIOL, V2, P155
[5]   The epithelial mucin, MUC1, is expressed on resting T lymphocytes and can function as a negative regulator of T cell activation [J].
Chang, JF ;
Zhao, HL ;
Phillips, J ;
Greenburg, G .
CELLULAR IMMUNOLOGY, 2000, 201 (02) :83-88
[6]   Antigenic cross-reactivity of human tracheal mucin with human sperm and trophoblasts correlates with the expression of mucin 8 gene messenger ribonucleic acid in reproductive tract tissues [J].
DCruz, OJ ;
Dunn, TS ;
Pichan, P ;
Haas, GG ;
Sachdev, GP .
FERTILITY AND STERILITY, 1996, 66 (02) :316-326
[7]  
Dyomin VG, 2000, BLOOD, V95, P2666
[8]  
GENDLER SJ, 1990, J BIOL CHEM, V265, P15286
[9]  
HO SB, 1993, CANCER RES, V53, P641
[10]  
HOLSTEIN AF, 1986, ANDROLOGIA, V18, P601