Zhang Jie, Chen Liang, Gu Yu-Dong
Department of Orthopedics, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
Department of Hand Surgery, Huashan Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai, China; Shanghai Key Laboratory of Peripheral Nerve and Microsurgery, Shanghai, China.
World Neurosurg. 2017 Oct;106:211-218. doi: 10.1016/j.wneu.2017.06.133. Epub 2017 Jun 30.
Major histocompatibility complex class I (MHCI), paired-immunoglobulin-like receptor B (PirB), and cluster of differentiation 3ζ (CD3ζ) negatively regulate neuronal plasticity in developing and adult brains. The aim of this study was to evaluate expressive changes of these factors in motor cortical representations of the brachial plexus (MCRBP) after total brachial plexus root avulsion (tBPRA).
A total of 45 rats were randomly and equally divided into 3 groups for evaluating mRNA and protein expression levels of MHCI, PirB, and CD3ζ: 7 days, 3 months, and control. In the 7-day and 3-month groups, expressions were examined at 7 days and 3 months, respectively, after left tBPRA. In the control group, the brachial plexus was uninjured. Three rats from each group were used for examining expressions of MHCI, PirB, and CD3ζ proteins by immunofluorescence labeling, 6 rats for quantification of MHCI, PirB, and CD3ζ mRNAs by real-time quantitative polymerase chain reaction, and the remaining 6 animals for quantification of MHCI, PirB, and CD3ζ proteins by Western blotting.
In the original MCRBP, mRNA and protein expression levels of MHCI, PirB, and CD3ζ were down-regulated 7 days postinjury compared with control (P < 0.01). Interestingly, mRNA and protein expression levels of these factors were up-regulated at 3 months compared with 7 days (P < 0.01), excepting PirB protein, whose expression was not increasing (P > 0.05). Recovery of protein expressions were initiated from near the border region of the original MCRBP.
MHCI, PirB, and CD3ζ may participate in motor cortical reorganization after tBPRA.
主要组织相容性复合体I类(MHCI)、配对免疫球蛋白样受体B(PirB)和分化簇3ζ(CD3ζ)对发育中和成年大脑中的神经元可塑性起负调节作用。本研究旨在评估全臂丛神经根撕脱伤(tBPRA)后,这些因子在臂丛神经运动皮质代表区(MCRBP)中的表达变化。
总共45只大鼠被随机等分为3组,用于评估MHCI、PirB和CD3ζ的mRNA和蛋白质表达水平:7天组、3个月组和对照组。在7天组和3个月组中,分别在左侧tBPRA术后7天和3个月检测表达情况。对照组的臂丛神经未受伤。每组取3只大鼠通过免疫荧光标记检测MHCI、PirB和CD3ζ蛋白的表达,6只大鼠通过实时定量聚合酶链反应对MHCI、PirB和CD3ζ mRNA进行定量,其余6只动物通过蛋白质免疫印迹法对MHCI、PirB和CD3ζ蛋白进行定量。
在原始MCRBP中,与对照组相比,损伤后7天MHCI、PirB和CD3ζ的mRNA和蛋白质表达水平下调(P < 0.01)。有趣的是,与7天相比,这些因子的mRNA和蛋白质表达水平在3个月时上调(P < 0.01),但PirB蛋白除外,其表达未增加(P > 0.05)。蛋白质表达的恢复从原始MCRBP的边界区域附近开始。
MHCI、PirB和CD3ζ可能参与tBPRA后的运动皮质重组。