High glucose up-regulates Semaphorin 3A expression via the mTOR signaling pathway in keratinocytes: A potential mechanism and therapeutic target for diabetic small fiber neuropathy.

Abstract

Small fiber neuropathy (SFN) is a common complication in diabetes, and is characterized by decreased intraepidermal nerve fiber density (IENFD). Semaphorin 3A (Sema3A), which is produced by keratinocytes, has a chemorepulsive effect on intraepidermal nerve fibers. mTOR signaling can mediate local protein synthesis that is critical for growth of axons and dendrites. Therefore, this study aimed to investigate whether Sema3A is up-regulated in diabetic keratinocytes via the mTOR-mediated p70 S6K and 4E-BP1 signaling pathways, and furthermore whether it is involved in the pathogenesis of diabetic SFN. IENFD, expression of Sema3A, and mTOR signaling, were evaluated in the skin of diabetic patients with SFN as well as control subjects. Sema3A and mTOR signaling were also assessed in HaCaT cells which had been treated with high glucose (HG) or recombinant Sema3A (rSema3A) in the presence or absence of rapamycin. Small fiber dysfunction was evaluated by examining IENFD and using behavioral tests in control and streptozotocin-induced diabetic rats treated with or without rapamycin. We found that higher Sema3A expression and over-activation of mTOR signaling, was accompanied by reduced IENFD in the skin of diabetic patients compared with control subjects. The expression of Sema3A, and mTOR signaling were up-regulated in HaCaT cells incubated with HG or rSema3A, and this could be attenuated by rapamycin. Hyperalgesia, reduced IENFD, and up-regulated Sema3A and mTOR signaling were also detected in diabetic rats. These effects were ameliorated by rapamycin treatment. Our data indicate that HG up-regulates Sema3A expression by activating mTOR signaling in diabetic keratinocytes. This pathway may therefore play a critical role in diabetic SFN.

• Authors: Liang-Yan Wu, Mei Li, Min-Li Qu, Xin Li, Lin-Hua Pi, Zi Chen, Shan-Lei Zhou, Xiao-Qing Yi, Xia-Jie Shi, Jing Wu, Shan Wang
• Journal: Molecular and cellular endocrinology (Mol Cell Endocrinol) Vol. 472 Pg. 107-116 (09 05 2018) ISSN: 1872-8057 [Electronic] Ireland
• PMID: 29203371 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2017 Elsevier B.V. All rights reserved.

Chemical References

• Blood Glucose
• Semaphorin-3A
• TOR Serine-Threonine Kinases
• Glucose
• Sirolimus

Topics

• Animals
• Blood Glucose (metabolism)
• Case-Control Studies
• Cell Line
• Diabetes Mellitus, Experimental (blood, metabolism, pathology)
• Diabetic Neuropathies (blood, drug therapy, pathology)
• Female
• Glucose (toxicity)
• Humans
• Hyperalgesia (pathology)
• Keratinocytes (drug effects, metabolism)
• Male
• Middle Aged
• Rats, Sprague-Dawley
• Semaphorin-3A (metabolism)
• Signal Transduction
• Sirolimus (pharmacology)
• Skin (innervation, pathology)
• Small Fiber Neuropathy (blood, drug therapy, pathology)
• TOR Serine-Threonine Kinases (metabolism)
• Up-Regulation (drug effects)