TMPRSS2, a Serine Protease Expressed in the Prostate on the Apical Surface of Luminal Epithelial Cells and Released into Semen in Prostasomes, Is Misregulated in Prostate Cancer Cells

被引:125
作者
Chen, Ya-Wen [1 ,2 ]
Lee, Ming-Shyue [5 ]
Lucht, Amanda [1 ]
Chou, Feng-Pai [1 ,3 ]
Huang, Wei [6 ,7 ]
Havighurst, Thomas C. [8 ]
Kim, KyungMann [8 ]
Wang, Jehng-Kang [9 ]
Antalis, Toni M. [1 ,4 ]
Johnson, Michael D. [10 ]
Lin, Chen-Yong [1 ,3 ]
机构
[1] Univ Maryland, Geenehaum Canc Ctr, Baltimore, MD 21201 USA
[2] Univ Maryland, Grad Program Life Sci, Baltimore, MD 21201 USA
[3] Univ Maryland, Dept Biochem & Mol Biol, Baltimore, MD 21201 USA
[4] Univ Maryland, Dept Physiol, Baltimore, MD 21201 USA
[5] Natl Taiwan Univ, Coll Med, Dept Biochem & Mol Biol, Taipei 10764, Taiwan
[6] Univ Wisconsin, Dept Pathol, Madison, WI 53792 USA
[7] Univ Wisconsin, Dept Lab Med, Madison, WI 53792 USA
[8] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI 53792 USA
[9] Natl Def Med Ctr, Dept Biochem, Taipei 10764, Taiwan
[10] Georgetown Univ, Dept Oncol, Lombardi Canc Comprehens Ctr, Washington, DC USA
关键词
PLASMA PREVENTS SPERM; SWIM-UP MEDIUM; HUMAN SPERMATOZOA; PROTEOLYTIC-ENZYMES; HUMAN-MILK; TRANSMEMBRANE; MOTILITY; MATRIPTASE; FUSION; INHIBITOR;
D O I
10.2353/ajpath.2010.090665
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
TMPRSS2, a type II transmembrane serine protease, is highly expressed by the epithelium of the human prostate gland. To explore the regulation and function of TMPRSS2 in the prostate, a panel of monoclonal antibodies with high sensitivity and specificity were generated. Immunodetection showed TMPRSS2 on the apical plasma membrane of the prostate luminal cells and demonstrated its release into semen as a component of prostasomes, organelle-like vesicles that may facilitate sperm function and enhance male reproduction. In prostate cancer cells, TMPRSS2 expression was increased and the protein mislocalized over the entire tumor cell membrane. In both LNCaP prostate cancer cells and human semen, TMPRSS2 protein was detected predominantly as inactive zymogen forms as part of an array of multiple noncovalent and disulfide-linked complexes, suggesting that TMPRSS2 activity may be regulated by unconventional mechanisms. Our data suggested that TMPRSS2, an apical surface serine protease, may have a normal role in male reproduction as a component of prostasomes. The aberrant cellular localization, and increased expression of the protease seen in cancer, may contribute to prostate tumorigenesis by providing access of the enzyme to nonphysiological substrates and binding-proteins. (Am J Pathol 2010, 176:2986-2996 DOI: 10.2353/ajpath.2010.090665)
引用
收藏
页码:2986 / 2996
页数:11
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