Published-Ahead-of-Print December 18, 2008, DOI:10.2164/jandrol.108.005934
Journal of Andrology, Vol. 30, No. 3, May/June 2009
Copyright © American Society of Andrology
DOI: 10.2164/jandrol.108.005934
Differential Gene Expression in the Testes of Different Murine Strains Under Normal and Hyperthermic Conditions
YING LI,
QING ZHOU,
RANDY HIVELY,
LIZHONG YANG,
CHRISTOPHER SMALL AND
MICHAEL D. GRISWOLD
From the Center for Reproductive Biology, School of Molecular
Biosciences, Washington State University, Pullman, Washington.
|
Correspondence to: Dr Michael D. Griswold, 531 Fulmer Hall, School of
Molecular Biosciences, Washington State University, Pullman, WA 99164 (e-mail:
griswold{at}mail.wsu.edu). |
Cryptorchidism and scrotal heating result in abnormal spermatogenesis, but
the mechanism(s) prescribing this temperature sensitivity are unknown. It was
previously reported that the AKR/N or MRL/MpJ-+/+ mouse testis is more
heat-resistant than the testis from the C57BL/6 strain. We have attempted to
probe into the mechanism(s) involved in heat sensitivity by examining global
gene expression profiles of normal and heat-treated testes from C57BL/6,
AKR/N, and MRL/MpJ-+/+ mice by microarray analysis. In the normal C57BL/6
testis, 415 and 416 transcripts were differentially expressed (at least 2-fold
higher or lower) when compared with the normal AKR/N and MRL/MpJ-+/+ testis,
respectively. The AKR/N and MRL/MpJ-+/+ strains revealed 268 differentially
expressed transcripts between them. There were 231 transcripts differentially
expressed between C57BL/6 and 2 purported heat-resistant strains, AKR/N and
MRL/MpJ-+/+. Next, the testes of C57BL/6 and AKR/N mice were exposed to
43°C for 15 minutes and harvested at different time points for terminal
deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) studies and
microarrays. An increase of TUNEL-positive germ cell numbers was significant 8
hours after heat exposure in the C57BL/6 mouse. However, this increase was not
observed in the AKR/N mouse until 10 hours after heat exposure. All tubules
showed germ cell loss and disruption in C57BL/6 testis 24 hours after heat
shock. In contrast, although a number of seminiferous tubules showed an
abnormal morphology 24 hours post–heat shock in the AKR/N mouse, many
tubules still retained a normal structure. Numerous transcripts exhibited
differential regulation between the 2 strains within 24 hours after heat
exposure. The differentially expressed transcripts in the testes 8 hours after
heat exposure were targeted to identify the genes involved in the initial
response rather than those attributable to germ cell loss. Twenty transcripts
were significantly down-regulated and 19 genes were up-regulated by
hyperthermia in C57BL/6 and did not show a parallel change in the AKR/N
testis. Conversely, heat shock resulted in 30 up-regulated transcripts and 31
down-regulated transcripts in AKR/N that were not similarly regulated in
C57BL/6. A number of genes shared similar differential expression patterns and
differential regulation by hyperthermia in both strains of mice. Taken
together, the results of the present study indicate that the diverse genetic
backgrounds in the 3 strains lead to major differences in normal testis gene
expression profiles, whereas the differences in heat shock responses involve a
significantly smaller number of genes. The data generated may provide insights
regarding gene networks and pathways involved in heat stress and their
relationship to spermatogenesis.
Key words: Heat stress, testis, mouse strain, AKR/N, C57BL/6, microarray analysis
This article has been cited by other articles:

|
 |

|
 |
 
C. Li, X. Wang, G. Wang, N. Li, and C. Wu
Expression analysis of global gene response to chronic heat exposure in broiler chickens (Gallus gallus) reveals new reactive genes
Poult. Sci.,
May 1, 2011;
90(5):
1028 - 1036.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. J. Hansen
Effects of heat stress on mammalian reproduction
Phil Trans R Soc B,
November 27, 2009;
364(1534):
3341 - 3350.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2009 by The American Society of Andrology.