Necrotic neuronal cells induce inflammatory Schwann cell activation via TLR2 and TLR3: Implication in Wallerian degeneration

被引:72
作者
Lee, Hyunkyoung
Jo, Eun-Kyeong
Choi, Se-Young
Oh, Seog Bae
Park, Kyungpyo
Kim, Joong Soo
Lee, Sung Joong
机构
[1] Seoul Natl Univ, Program Neurosci, DRI, Sch Dent, Seoul 110749, South Korea
[2] Seoul Natl Univ, Dept Oral Physiol, Sch Dent, Seoul 110749, South Korea
[3] Chungnam Natl Univ, Dept Microbiol, Coll Med, Taejon, South Korea
基金
新加坡国家研究基金会;
关键词
Schwann cells; toll-like receptor; iNOS; TNF-alpha; Wallerian degeneration;
D O I
10.1016/j.bbrc.2006.09.108
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Schwann cells play an important role in peripheral nerve regeneration. Upon nerve injury, Schwann cells are activated and produce various proinflammatory cytokines and chemokines, resulting in the recruitment of macrophages and the phagocytosis of myelin debris. However, it is unclear how nerve injury induces Schwann cell activation. Recently, it was reported that necrotic cells induce immune cell activation via toll-like receptors (TLRs). This suggests that the TLRs expressed on Schwann cells may recognize nerve injury by binding to the endogenous ligands secreted by the damaged nerve, thereby inducing Schwann cell activation. To explore such a possibility, we stimulated rat Schwann cells with necrotic neuronal cells (NNC). The stimulation of Schwann cells with NNC induced the expression of various inflammatory mediators, including TNF-alpha and iNOS. Studies on the NNC-mediated intracellular signaling pathways revealed that p38 and JNK are involved in the NNC-mediated Schwann cell activation. In addition, NNC-induced proinflammatory gene expression was reduced in mouse Schwann cells derived from TLR2 or TLR3 knockout mice. In summary, these results suggest that necrotic neuronal cells induce inflammatory Schwann cell activation via TLR2 and TLR3, which might be involved in Wallerian degeneration upon peripheral nerve injury. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:742 / 747
页数:6
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