Absence of mechanical allodynia and Aβ‐fiber sprouting after sciatic nerve injury in mice lacking membrane‐type 5 matrix metalloproteinase

坐骨神经 痛觉超敏 神经病理性疼痛 神经损伤 脊髓 伤害 周围神经损伤 神经科学 基质金属蛋白酶 解剖 神经系统 病理 化学 医学 生物 内科学 痛觉过敏 受体
作者
Kiyoshi Komori,Takahiro Nonaka,Akiko Okada,Hiroaki Kinoh,Hiromi Hayashita-Kinoh,Nobuaki Yoshida,Ikuo Yana,Motoharu Seiki
出处
期刊:FEBS Letters [Wiley]
卷期号:557 (1-3): 125-128 被引量:67
标识
DOI:10.1016/s0014-5793(03)01458-3
摘要

Matrix metalloproteinases (MMPs) are a family of endopeptidases that degrade extracellular matrix components. Membrane-type 5 MMP (MT5-MMP/MMP-24) was identified as neuron-specific, and is believed to contribute to neuronal circuit formation and plasticity. To elucidate its function in vivo, we have generated mice lacking MT5-MMP by gene targeting. MT5-MMP-deficient mice were born without obvious morphological abnormalities. No apparent histological defects were observed in the nervous system either. However, MT5-MMP-deficient mice did not develop neuropathic pain with mechanical allodynia after sciatic nerve injury, though responses to acute noxious stimuli were normal. Neuropathic pain induced by peripheral nerve lesions is known to accompany structural reorganization of the nervous system. Intraneural injection of cholera toxin B subunit, a transganglionic tracer, into the injured sciatic nerve of wild-type mice revealed that the myelinated Abeta-fiber primary afferents sprouted from laminae III-VI of the dorsal horn of the spinal cord and invaded lamina II. However, no such sprouting and invasion of Abeta-fibers were observed in MT5-MMP-deficient mice. These findings suggest that MT5-MMP is essential for the development of mechanical allodynia and plays an important role in neuronal plasticity in this mouse model.
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