Interactions of Notch1 and TLR4 signaling pathways in DRG neurons of in vivo and in vitro models of diabetic neuropathy.

Abstract

Understanding the interactions between Notch1 and toll-like receptor 4 (TLR4) signaling pathways in the development of diabetic peripheral neuropathy may lead to interpretation of the mechanisms and novel approaches for preventing diabetic neuropathic pain. In the present study, the interactions between Notch1 and TLR4 signaling pathways were investigated by using dorsal root ganglion (DRG) from diabetic neuropathic pain rats and cultured DRG neurons under high glucose challenge. The results showed that high glucose induced not only Notch1 mRNA, HES1 mRNA, and TLR4 mRNA expression, but also Notch1 intracellular domain (NICD1) and TLR4 protein expression in DRG neurons. The proportion of NICD1-immunoreactive (IR) and TLR4-IR neurons in DRG cultures was also increased after high glucose challenge. The above alterations could be partially reversed by inhibition of either Notch1 or TLR4 signaling pathway. Inhibition of either Notch1 or TLR4 signaling pathway could improve mechanical allodynia and thermal hyperalgesia thresholds. Inhibition of Notch1 or TLR4 signaling also decreased tumor necrosis factor-α (TNF-α) levels in DRG from diabetic neuropathic rats. These data imply that the interaction between Notch1 and TLR4 signaling pathways is one of the important mechanisms in the development or progression of diabetic neuropathy.

• Authors: Tianhua Chen, Hao Li, Yiting Yin, Yuanpin Zhang, Zhen Liu, Huaxiang Liu
• Journal: Scientific reports (Sci Rep) Vol. 7 Issue 1 Pg. 14923 (11 02 2017) ISSN: 2045-2322 [Electronic] England
• PMID: 29097792 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• RNA, Messenger
• Receptor, Notch1
• Toll-Like Receptor 4

Topics

• Animals
• Diabetic Neuropathies (genetics, metabolism, pathology)
• Disease Models, Animal
• Disease Progression
• Ganglia, Spinal (cytology, metabolism, pathology)
• Hyperalgesia (genetics, metabolism, pathology)
• Male
• Neuralgia (genetics, metabolism, pathology)
• Neurons (metabolism, pathology)
• Protein Interaction Maps
• RNA, Messenger (genetics)
• Rats
• Rats, Wistar
• Receptor, Notch1 (genetics, metabolism)
• Signal Transduction
• Toll-Like Receptor 4 (genetics, metabolism)