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Effects of over-expression of TLR2 in transgenic goats on pathogen clearance and role of up-regulation of lysozyme secretion and infiltration of inflammatory cells

Authors :
Hongtao Zhang
Zhengxing Lian
Maosheng Cui
Hai-Juan He
Yuchang Yao
Yu-Feng Liu
Ning Li
Bao-Lu Zhang
Shou-Long Deng
Juncai Fu
Kun Yu
Source :
BMC Veterinary Research, Vol 8, Iss 1, p 196 (2012), BMC Veterinary Research
Publication Year :
2012
Publisher :
BMC, 2012.

Abstract

Background Toll-like receptor 2 (TLR2) is important to host recognition of invading gram-positive microbes. In goats, these microbes can cause serious mastitis, anthrax, tetanus, and other problems. Transgenic goats constitutively over-expressing TLR2 in many tissues serve as a suitable model for the study of the role of TLR2 over-expression in bacterial clearance. Results Capra hircus TLR2 over-expression vector (p3S-LoxP-TLR2) was used to generate transgenic goats by egg microinjection. The integration efficiency was 8.57%. Real-time PCR and immunohistochemical results confirmed that the goats over-expressing the TLR2 gene (Tg) expressed more TLR2 than wild-type goats (WT). Monocyte-macrophages from the bloodstreams of transgenic goats were stimulated with synthetic bacterial lipoprotein (Pam3CSK4) and by the promotion of interleukin-6 (IL-6) and IL-10 expression in vitro. The oxidative damage was significantly reduced, and lysozyme (LZM) secretion was found to be up-regulated. Ear tissue samples from transgenic goats that had been stimulated with Pam3CSK4 via hypodermic injection showed that transgenic individuals can undergo the inflammation response very quickly. Conclusions Over-expression of TLR2 was found to decrease radical damage to host cells through low-level production of NO and MDA and to promote the clearance of invasive bacteria by up-regulating lysozyme secretion and filtration of inflammatory cells to the infected site.

Details

Language :
English
ISSN :
17466148
Volume :
8
Issue :
1
Database :
OpenAIRE
Journal :
BMC Veterinary Research
Accession number :
edsair.doi.dedup.....1bcd82ba6bf40924a528ed16a4dc3e6d