Sperm mitochondrial DNA depletion in men with asthenospermia

被引:71
作者
Kao, SH
Chao, HT
Liu, HW
Liao, TL
Wei, YH
机构
[1] Natl Yang Ming Univ, Dept Biochem, Sch Life Sci, Taipei 112, Taiwan
[2] Taipei Med Univ, Grad Inst Biomed Technol, Taipei, Taiwan
[3] Taipei Vet Gen Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[4] Natl Def Med Ctr, Dept Biol & Anat, Taipei, Taiwan
关键词
depletion; infertility; mitochondrial DNA; motility; sperm;
D O I
10.1016/j.fertnstert.2003.11.056
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To determine the content of sperm mitochondrial DNA (mtDNA) in patients with asthenospermia or with poor sperm motility. Design: Analysis of the content of mtDNA as the ratio between the amount of mtDNA and nuclear DNA by using a new concurrent polymerase chain reaction. Setting: University hospital infertility center. Patient(s): Eighty-six men who sought infertility therapy. Intervention(s): Moving characteristics of sperm were examined with a computer-assisted semen analyzer. Main Outcome Measure(s): Sperm samples were classified into two groups, one with asthenospermia and the other with normal moving characteristics. The content of mtDNA in sperm was determined by polymerase chain reaction. We analyzed the mitochondrial mass by MitoTracker Green staining and analyzed DNA content with propidium iodide staining by flow cytometry. Result(s): A decrease in sperm mtDNA content was detected in patients with asthenospermia or with poor sperm motility (<20% motility). The relative mtDNA contents in the asthenospermia and normal groups were 7.2 +/- 1.3 (mean +/- SD, n = 23) and 74.1 +/- 2.0 (n = 29), respectively. Lower intensities of propidium iodide staining were detected in patients with asthenospermia or poor motility, but there was no significant difference in MitoTracker Green staining between the sperm with different motility. Conclusion(s): We suggest that mtDNA content may serve as a useful indicator of sperm quality and that mtDNA depletion may play an important role in the pathophysiology of some male infertility. (C) 2004 by American Society for Reproductive Medicine.
引用
收藏
页码:66 / 73
页数:8
相关论文
共 33 条
[1]   Misconceptions about mitochondria and mammalian fertilization: Implications for theories on human evolution [J].
AnkelSimons, F ;
Cummins, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13859-13863
[2]   D-loop mutations in mitochondrial DNA:: link with mitochondrial DNA depletion? [J].
Barthélémy, C ;
de Baulny, HO ;
Lombès, A .
HUMAN GENETICS, 2002, 110 (05) :479-487
[3]   The inheritance of genes in mitochondria and chloroplasts: Laws, mechanisms, and models [J].
Birky, CW .
ANNUAL REVIEW OF GENETICS, 2001, 35 :125-148
[4]  
Cummins JM, 1998, INT J ANDROL, V21, P47
[5]  
DELAMIRANDE E, 1992, J ANDROL, V13, P379
[6]   Mitochondrial DNA content of human spermatozoa [J].
Díez-Sánchez, C ;
Ruiz-Pesini, E ;
Lapeña, AC ;
Montoya, J ;
Pérez-Martos, A ;
Enríquez, JA ;
López-Pérez, MJ .
BIOLOGY OF REPRODUCTION, 2003, 68 (01) :180-185
[7]   Energetic communication between mitochondria and nucleus directed by catalyzed phosphotransfer [J].
Dzeja, PP ;
Bortolon, R ;
Perez-Terzic, C ;
Holmuhamedov, EL ;
Terzic, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) :10156-10161
[8]   MATERNAL INHERITANCE OF THE MOUSE MITOCHONDRIAL GENOME IS NOT MEDIATED BY A LOSS OR GROSS ALTERATION OF THE PATERNAL MITOCHONDRIAL-DNA OR BY METHYLATION OF THE OOCYTE MITOCHONDRIAL-DNA [J].
HECHT, NB ;
LIEM, H ;
KLEENE, KC ;
DISTEL, RJ ;
HO, SM .
DEVELOPMENTAL BIOLOGY, 1984, 102 (02) :452-461
[9]   Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa [J].
Kao, SH ;
Chao, HT ;
Wei, YH .
MOLECULAR HUMAN REPRODUCTION, 1998, 4 (07) :657-666
[10]   MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID 4977-BP DELETION IS ASSOCIATED WITH DIMINISHED FERTILITY AND MOTILITY OF HUMAN SPERM [J].
KAO, SH ;
CHAO, HT ;
WEI, YH .
BIOLOGY OF REPRODUCTION, 1995, 52 (04) :729-736