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慢性前列腺炎影响男性生殖健康,并与C-X-C基序趋化因子12受体C-X-C趋化因子受体4的全身和局部表观遗传失活有关。

Chronic Prostatitis Affects Male Reproductive Health and Is Associated with Systemic and Local Epigenetic Inactivation of C-X-C Motif Chemokine 12 Receptor C-X-C Chemokine Receptor Type 4.

作者信息

Schagdarsurengin Undraga, Teuchert Lisa M, Hagenkötter Christina, Nesheim Nils, Dansranjavin Temuujin, Schuppe Hans-Christian, Gies Sabrina, Pilatz Adrian, Weidner Wolfgang, Wagenlehner Florian M E

机构信息

Clinic of Urology, Justus-Liebig-University Giessen, Giessen, Germany.

出版信息

Urol Int. 2017;98(1):89-101. doi: 10.1159/000452251. Epub 2016 Oct 20.

Abstract

UNLABELLED

Background/Aims/Objectives: Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) has detrimental effects on the quality of life including the aspect of sexual dysfunction. The aim of the study was to identify if there was an adverse effect on the male genital compartment and if there are systemic or compartment-specific local signals for epigenetic dysregulation of inflammatory factors in CP/CPPS patients.

METHODS

One hundred five NIH IIIb CP/CPPS patients and 41 healthy men were recruited and underwent investigations of urines, semen and blood. Promoter methylation and expression of the chemokine C-X-C motif chemokine 12 and its receptor C-X-C chemokine receptor type 4 (CXCR4) (involved in the recruitment of mast cells) were analyzed in prostate epithelial cell lines and in healthy volunteers' and patients' blood, ejaculate cell pellets, and separated ejaculate fractions (sperm and seminal somatic cells).

RESULTS

Independently from age, CP/CPPS NIH IIIb was associated with significant impairment of sperm motility, morphology and semen pH (p < 0.001). Patients older than 33 years showed significantly increased seminal interleukin-8 and serum prostate specific antigen values. In patients, the CXCR4 mRNA-expression was significantly decreased in whole blood and ejaculate cell pellets due to promoter hypermethylation. Analyses on separated fractions of sperm and seminal somatic cells revealed that sperm DNA was unaffected, whereas somatic cell DNA was differentially methylated.

CONCLUSIONS

NIH IIIb CP/CPPS has negative effects on surrogate parameters of male fertility and is associated significantly with systemic and local epigenetic inactivation of CXCR4.

摘要

未标注

背景/目的/目标:慢性前列腺炎/慢性盆腔疼痛综合征(CP/CPPS)对生活质量有不利影响,包括性功能方面。本研究的目的是确定CP/CPPS患者是否对男性生殖器官有不良影响,以及是否存在全身性或特定器官局部信号导致炎症因子表观遗传失调。

方法

招募了105名NIH IIIb型CP/CPPS患者和41名健康男性,对其尿液、精液和血液进行检测。分析了前列腺上皮细胞系以及健康志愿者和患者的血液、射精细胞沉淀和分离的射精成分(精子和精浆体细胞)中趋化因子C-X-C基序趋化因子12及其受体C-X-C趋化因子受体4型(CXCR4)(参与肥大细胞募集)的启动子甲基化和表达情况。

结果

独立于年龄,NIH IIIb型CP/CPPS与精子活力、形态和精液pH值的显著受损相关(p < 0.001)。33岁以上患者的精液白细胞介素-8和血清前列腺特异性抗原值显著升高。在患者中,由于启动子高甲基化,全血和射精细胞沉淀中的CXCR4 mRNA表达显著降低。对精子和精浆体细胞分离成分的分析表明,精子DNA未受影响,而体细胞DNA存在差异甲基化。

结论

NIH IIIb型CP/CPPS对男性生育的替代参数有负面影响,并且与CXCR4的全身性和局部表观遗传失活显著相关。

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