Processing of seminal plasma hCAP-18 to ALL-38 by gastricsin - A novel mechanism of generating antimicrobial peptides in vagina

被引:130
作者
Sorensen, OE
Gram, L
Johnsen, AH
Andersson, E
Bangsboll, S
Tjabringa, GS
Hiemstra, PS
Malm, J
Egesten, A
Borregaard, N
机构
[1] Univ Copenhagen Hosp, Granulocyte Res Lab, Dept Hematol, Rigshosp, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen Hosp, Dept Clin Biochem, Rigshosp, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen Hosp, Fertil Clin, Rigshosp, DK-2100 Copenhagen, Denmark
[4] Danish Inst Fisheries Res, Dept Seafood Res, DK-2800 Lyngby, Denmark
[5] Malmo Univ Hosp, Dept Lab Med, SE-20502 Malmo, Sweden
[6] Leiden Univ, Dept Lab Med, Med Ctr, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1074/jbc.M301608200
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 human cathelicidin, hCAP-18, is expressed both in neutrophils and in epithelial cells. hCAP-18 is processed to the antimicrobial peptide LL-37 by proteinase 3 in neutrophils. hCAP-18 is highly expressed in the epididymis with a subsequent high concentration in seminal plasma where the protein is present in its unprocessed and antimicrobially inactive form. We report here that hCAP-18 in seminal plasma is processed to generate a 38-amino acid antimicrobial peptide ALL-38 by the prostate-derived protease gastricsin when incubated at a pH corresponding to the vaginal pH. In accordance with this, seminal plasma derived hCAP-18 was found in its processed form in the vagina following sexual intercourse. The antimicrobial activity of ALL-38 against a variety of microorganisms tested is equal to that of LL37. This enzymatic activation of a proantimicrobial substance in seminal plasma following exposure to the vaginal milieu represents a novel mechanism to prevent infection following sexual intercourse.
引用
收藏
页码:28540 / 28546
页数:7
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