Abstract
This study sought to identify sources of the reduced fertility of men with type 2 diabetes mellitus. Significant reductions in semen volume, sperm concentration, and total sperm count were observed in diabetic individuals, while transmission electron microscopy revealed that the structure of mitochondria in the tail of sperm from diabetic patients was damaged. Proteins potentially associated with these sperm defects were identified using proteomics. Isobaric tagging for relative and absolute quantitation labeling and high-performance liquid chromatography-tandem mass spectrometry allowed us to identify 357 proteins significantly differentially expressed in diabetic versus control semen (>1.2 or <0.83). According to gene ontology enrichment and pathway analyses, many of these differentially expressed proteins are associated with sperm function, including binding of sperm to the zona pellucida and proteasome function; of particular interest, half of these proteins were related to mitochondrial metabolism. Protein-interaction networks revealed that a decrease in Cystatin C and Dipeptidyl peptidase 4 in the mitochondria may be sources of the decreased motility of sperm from diabetic patients.
Keywords
diabetes mellitus
male infertility
mitochondrial metabolism
sperm proteomics
MeSH Terms
Adult
Apoptosis Inducing Factor/analysis
Biomarkers/analysis
Chromatography, High Pressure Liquid
Cystatin C/analysis
Diabetes Mellitus, Type 2/etiology,pathology
Dipeptidyl Peptidase 4/analysis
Fertility/physiology
Humans
Infertility, Male/complications,pathology
Male
Middle Aged
Mitochondria/metabolism
Mitochondrial Proteins/analysis
Semen Analysis
Sperm Count
Sperm Motility/physiology
Spermatozoa/physiology
Tandem Mass Spectrometry
Chemicals
AIFM1 protein, human
Apoptosis Inducing Factor
Biomarkers
Cystatin C
Mitochondrial Proteins
Dipeptidyl Peptidase 4
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
An Tian
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.
Wang Yue-Fen
Beijing Hospital of Traditional Chinese Medicine, Beijing, China.
Liu Jia-Xian
Leonard Davis School of Gerontology, University of Southern California, Los Angeles, California.
Pan Yan-Yun
ORCID
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.
Liu Yu-Fei
Beijing University of Chinese Medicine 3rd Affiliated Hospital, Beijing, China.
He Zhong-Chen
Department of Endocrine, Beijing He ping li Hospital, Beijing, China.
Mo Fang-Fang
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.
Li Jun
Department of Endocrine, Beijing He ping li Hospital, Beijing, China.
Kang Li-Hua
Department of Endocrine, Beijing He ping li Hospital, Beijing, China.
Gu Yu-Jie
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.
Lv Bo-Han
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.
Gao Si-Huan
ORCID
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.
Jiang Guang-Jian
Diabetes Research Center, Beijing University of Chinese Medicine, Beijing, China.