Comparison of four fluorochromes for the detection of the inner mitochondrial membrane potential in human spermatozoa and their correlation with sperm motility

被引:155
作者
Marchetti, C
Jouy, N
Leroy-Martin, B
Defossez, A
Formstecher, P
Marchetti, P
机构
[1] Fac Med Lille, INSERM, U459, F-59045 Lille, France
[2] Fac Med Lille, Histol Lab, F-59045 Lille, France
[3] Fac Med Lille, IMPRT, IFR 114, F-59045 Lille, France
[4] Hop Jeanne de Flandre, Lab Biol Reprod, F-59037 Lille, France
关键词
flow cytometry; IVF; mitochondria; spermatozoa;
D O I
10.1093/humrep/deh416
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Sperm motility evaluation is associated with fertility in IVF programmes. The visual estimation of sperm motility is extremely subjective. Hence, alternative methods are required. Among them, determination of mitochondrial membrane potential (Deltapsi(m)) changes of spermatozoa using potentiometric dyes may be a reliable test to determine sperm quality. However, the use of the potentiometric dyes in sperm samples has not been compared. METHODS: We have studied sperm samples from 28 infertile patients enrolled in an IVF programme in flow cytometry after staining of spermatozoa with four commonly used potentiometric dyes. Sperm motility was evaluated visually. RESULTS: As expected, JC-1 seems to detect specifically Deltapsi(m) changes, CMX-Ros, DiOC(6)(3) and TMRE fluorescence is easily analysed and the latter three fluorochromes are particularly suitable for multiparametric staining. Irrespective of the Deltapsi(m)-dependent fluorochromes used to stain spermatozoa, a positive correlation was found between the percentage of Deltapsi(m)(high) cells and forward motility and also with high fertilization rates after IVF. CONCLUSION: The four fluorochromes may be useful for evaluation of sperm samples from infertile patients. The choice of the potentiometric dyes will depend on their fluorescence characteristics in order to use them in combination with other fluorescent markers.
引用
收藏
页码:2267 / 2276
页数:10
相关论文
共 28 条
[1]   Functional heterogeneity of an isolated mitochondrial population revealed by cytofluorometric analysis at the single organelle level [J].
Cossarizza, A ;
Ceccarelli, D ;
Masini, A .
EXPERIMENTAL CELL RESEARCH, 1996, 222 (01) :84-94
[2]   Differences in nuclear DNA fragmentation and mitochondrial integrity of semen and prepared human spermatozoa [J].
Donnelly, ET ;
O'Connell, M ;
McClure, N ;
Lewis, SEM .
HUMAN REPRODUCTION, 2000, 15 (07) :1552-1561
[3]  
Ferlini C, 1998, CYTOMETRY, V31, P74, DOI 10.1002/(SICI)1097-0320(19980101)31:1<74::AID-CYTO10>3.0.CO
[4]  
2-V
[5]   Fluorometric assessments of mitochondrial function and viability in cryopreserved bovine spermatozoa [J].
Garner, DL ;
Thomas, CA ;
Joerg, HW ;
DeJarnette, JM ;
Marshall, CE .
BIOLOGY OF REPRODUCTION, 1997, 57 (06) :1401-1406
[6]   Assessment of sperm quality: a flow cytometric approach [J].
Graham, JK .
ANIMAL REPRODUCTION SCIENCE, 2001, 68 (3-4) :239-247
[7]  
Gravance CG, 2001, REPROD TOXICOL, V15, P5, DOI 10.1016/S0890-6238(00)00113-1
[8]   Assessment of equine sperm mitochondrial function using JC-1 [J].
Gravance, CG ;
Garner, DL ;
Baumber, J ;
Ball, BA .
THERIOGENOLOGY, 2000, 53 (09) :1691-1703
[9]   Glucose induces a Na+,K+-ATPase-dependent transient hyperpolarization in human sperm.: I.: Induction of changes in plasma membrane potential by the proton ionophore CCCP [J].
Guzmán-Grenfell, AM ;
Bonilla-Hernández, MA ;
González-Martínez, MT .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1464 (02) :188-198
[10]   Functional assay of multidrug resistant cells using JC-1, a carbocyanine fluorescent probe [J].
Kuhnel, JM ;
Perrot, JY ;
Faussat, AM ;
Marie, JP ;
Schwaller, MA .
LEUKEMIA, 1997, 11 (07) :1147-1155