Department of Clinical Laboratory, The Second Affiliated Hospital of Nantong University, Nantong, 226001, People's Republic of China.
J Mol Neurosci. 2013 Mar;49(3):531-8. doi: 10.1007/s12031-012-9916-0. Epub 2012 Nov 9.
C-terminal binding protein 2 (CtBP2), as a transcriptional repressor, plays an essential role in development and tumorigenesis. However, its distribution and function in peripheral system lesion and repair are still unknown. Here, we investigated the spatiotemporal expression of CtBP2 in rat sciatic nerve crush model. Western blot analysis revealed that CtBP2 was expressed in normal sciatic nerve. It gradually decreased, reached minimal levels at 7 days after crush, and then returned to the normal level at 4 weeks. We observed that CtBP2 is mainly expressed in Schwann cells (SCs). In vitro, we induced SC differentiation via cyclic adenosine monophosphate (cAMP) and found that CtBP2 expression was downregulated during the process of differentiation. CtBP2-specific siRNA inhibited the cAMP-induced expression of the immature SC marker P75(NTR), and exogenous CtBP2 expression upregulated the expression of P75(NTR). Taken together, we hypothesized that peripheral nerve crush-induced downregulation of CtBP2 in the sciatic nerve was associated with SC differentiation, and CtBP2 likely played an important role in peripheral nerve injury and regeneration.
C 端结合蛋白 2(CtBP2)作为一种转录抑制因子,在发育和肿瘤发生中发挥着重要作用。然而,其在外周系统损伤和修复中的分布和功能仍不清楚。在这里,我们研究了 CtBP2 在大鼠坐骨神经挤压模型中的时空表达。Western blot 分析显示 CtBP2 在正常坐骨神经中表达。它逐渐减少,在挤压后 7 天达到最低水平,然后在 4 周时恢复到正常水平。我们观察到 CtBP2 主要在施万细胞(SCs)中表达。在体外,我们通过环磷酸腺苷(cAMP)诱导 SC 分化,发现 CtBP2 的表达在分化过程中下调。CtBP2 特异性 siRNA 抑制 cAMP 诱导的不成熟 SC 标志物 P75(NTR)的表达,而外源性 CtBP2 表达上调 P75(NTR)的表达。综上所述,我们假设坐骨神经挤压诱导 CtBP2 在坐骨神经中的下调与 SC 分化有关,CtBP2 可能在外周神经损伤和再生中发挥重要作用。