Expression of the HSPA2 gene in ejaculated spermatozoa from adolescents with and without varicocele

被引:59
作者
Lima, Samira Barbosa
Cenedeze, Marcos Antonio
Bertolla, Ricardo Pimenta
Hassun Filho, Pericles Assad
Oehninger, Sergio
Cedenho, Agnaldo Pereira
机构
[1] Univ Fed Sao Paulo, Dept Surg, Div Urol, BR-04025010 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Dept Med, Div Nephrol, BR-04025010 Sao Paulo, Brazil
[3] Eastern Virginia Med Sch, Jones Inst Reprod Med, Norfolk, VA 23501 USA
关键词
varicocele; heat stress; HSPA2; sperm; infertility;
D O I
10.1016/j.fertnstert.2006.05.030
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To evaluate mRNA expression of the HSPA2 gene in ejaculated spermatozoa in adolescents with and without varicocele. Design: Controlled prospective study. Setting: Patients in an academic research environment. Patients: Adolescent patients with clinical diagnosed bilateral varicocele grades II and III, and adolescent patients without varicocele. Intervention: Reverse-transcription-polymerase chain reaction (RT-PCR) analysis of HSPA2 gene expression in adolescents with and without varicocele. Main Outcome Measure: Comparative RT-PCR expression analysis of HSPA2 gene mRNA pared to the housekeeping beta-actin gene. Results: Sperm from adolescents with varicocele and oligozoospermia had significantly lower levels of HSPA2 Gene expression than both adolescents without varicocele (controls) and adolescents with varicocele and normal sperm concentration (P < .05). The latter group had a nonsignificant increase in gene expression compared to the control group. Conclusions: This is the first report on HSPA2 gene expression in ejaculated spermatozoa from adolescents and its relationship with varicocele pathology. Results demonstrated that, HSPA2. expression was down-regulated in adolescents with varicocele and oligozoospermia compared to controls. There was a higher, albeit nonsignificant, an in controls gene expression in adolescents with varicocele and normal sperm concentration than in controls. We speculate that expression levels of this gene might be used as a molecular marker for the acquisition of thermal tolerance in ejaculated spermatozoa.
引用
收藏
页码:1659 / 1663
页数:5
相关论文
共 25 条
[1]   Expression of stress response genes in germ cells during spermatogenesis [J].
Aguilar-Mahecha, A ;
Hales, BF ;
Robaire, B .
BIOLOGY OF REPRODUCTION, 2001, 65 (01) :119-127
[2]   Adolescents with varicocele have an impaired sperm-zona pellucida binding capacity [J].
Cedenho, AP ;
Spaine, DM ;
Barradas, V ;
Srougi, M ;
Oehninger, S .
FERTILITY AND STERILITY, 2002, 78 (06) :1339-1340
[3]  
DAHL EV, 1959, SURG GYNECOL OBSTET, V108, P697
[4]   Targeted gene disruption of Hsp70-2 results in failed meiosis, germ cell apoptosis, and male infertility [J].
Dix, DJ ;
Allen, JW ;
Collins, BW ;
Mori, C ;
Nakamura, N ;
PoormanAllen, P ;
Goulding, EH ;
Eddy, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3264-3268
[5]   Decreased expression of the heat shock protein hsp70-2 is associated with the pathogenesis of male infertility [J].
Feng, HL ;
Sandlow, JI ;
Sparks, AET .
FERTILITY AND STERILITY, 2001, 76 (06) :1136-1139
[6]  
GEORGOPOULOS C, 1993, ANNU REV CELL BIOL, V9, P601, DOI 10.1146/annurev.cellbio.9.1.601
[7]   ELEVATION OF INTRATESTICULAR AND SCROTAL SKIN SURFACE-TEMPERATURE IN MEN WITH VARICOCELE [J].
GOLDSTEIN, M ;
EID, JF .
JOURNAL OF UROLOGY, 1989, 142 (03) :743-745
[8]   THE HEAT-SHOCK COGNATE PROTEIN FROM DICTYOSTELIUM AFFECTS ACTIN POLYMERIZATION THROUGH INTERACTION WITH THE ACTIN-BINDING PROTEIN CAP32/34 [J].
HAUS, U ;
TROMMLER, P ;
FISHER, PR ;
HARTMANN, H ;
LOTTSPEICH, F ;
NOEGEL, AA ;
SCHLEICHER, M .
EMBO JOURNAL, 1993, 12 (10) :3763-3771
[9]   Putative creatine kinase M-isoform in human sperm is identified as the 70-kilodalton heat shock protein HspA2 [J].
Huszar, G ;
Stone, K ;
Dix, D ;
Vigue, L .
BIOLOGY OF REPRODUCTION, 2000, 63 (03) :925-932
[10]   Male subfertility induced by acute scrotal heating affects embryo quality in normal female mice [J].
Jannes, P ;
Spiessens, C ;
Van der Auwera, I ;
D'Hooghe, T ;
Verhoeven, G ;
Vanderschueren, D .
HUMAN REPRODUCTION, 1998, 13 (02) :372-375