Article

Toll-like receptor 3-initiated antiviral responses in mouse male germ cells in vitro.

Department of Cell Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing, China.
Biology of Reproduction (impact factor: 4.01). 01/2012; 86(4):106. DOI:10.1095/biolreprod.111.096719 pp.106
Source: PubMed

ABSTRACT The testis is an immunoprivileged site where local cell-initiated innate immunity plays a crucial role in antimicrobial responses. Toll-like receptors (TLRs) mediate innate immune responses in testicular somatic cells. Although several TLRs are expressed in some stages of male germ cells, the potential role of TLRs in triggering antimicrobial responses in the germ cells has yet to be exclusively studied. The current study demonstrates that TLR3 is constitutively expressed in spermatogonia and spermatocytes and can be activated by a synthetic double-strained RNA analog, polyinosinic-polycytidylic acid. TLR3 activation in these male germ cells up-regulates the expression of proinflammatory cytokines, such as interleukin IL1B, IL6, and tumor necrosis factor alpha, through activation of nuclear factor kappa B; it also induces production of type 1 interferons (IFNA and IFNB) through the activation of IFN regulatory factor 3. In addition, TLR3 activation increases the production of two major antiviral proteins, namely, double-stranded RNA-activated protein kinase and MX1 protein, by germ cells. Data in this article describe an antiviral response of male germ cells through the activation of TLR3 in vitro.

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Keywords

double-stranded RNA-activated protein kinase
 
germ cells
 
IFN regulatory factor 3
 
immunoprivileged site
 
local cell-initiated innate immunity
 
major antiviral proteins
 
male germ cells
 
male germ cells up-regulates
 
MX1 protein
 
nuclear factor kappa B
 
polyinosinic-polycytidylic acid
 
potential role
 
proinflammatory cytokines
 
spermatogonia
 
synthetic double-strained RNA analog
 
testicular somatic cells
 
TLR3 activation
 
Toll-like receptors
 
tumor necrosis factor alpha
 
type 1 interferons
 

Tao Wang