Chernov Andrei V, Dolkas Jennifer, Hoang Khang, Angert Mila, Srikrishna Geetha, Vogl Thomas, Baranovskaya Svetlana, Strongin Alex Y, Shubayev Veronica I
From the Sanford-Burnham Medical Research Institute, La Jolla, California 92037.
the Department of Anesthesiology, University of California, San Diego, La Jolla, California 92093, the Veterans Affairs San Diego Healthcare System, La Jolla, California 92037.
J Biol Chem. 2015 May 1;290(18):11771-84. doi: 10.1074/jbc.M114.622316. Epub 2015 Mar 19.
To shed light on the early immune response processes in severed peripheral nerves, we performed genome-wide transcriptional profiling and bioinformatics analyses of the proximal (P, regenerating) and distal (D, degenerating) nerve stumps on day 1 in the sciatic nerve axotomy model in rats. Multiple cell death-related pathways were activated in the degenerating D stump, whereas activation of the cytoskeletal motility and gluconeogenesis/glycolysis pathways was most prominent in the P stump of the axotomized nerve. Our bioinformatics analyses also identified the specific immunomodulatory genes of the chemokine, IL, TNF, MHC, immunoglobulin-binding Fc receptor, calcium-binding S100, matrix metalloproteinase, tissue inhibitor of metalloproteinase, and ion channel families affected in both the P and D segments. S100a8 and S100a9 were the top up-regulated genes in both the P and D segments. Stimulation of cultured Schwann cells using the purified S100A8/A9 heterodimer recapitulated activation of the myeloid cell and phagocyte chemotactic genes and pathways, which we initially observed in injured nerves. S100A8/A9 heterodimer injection into the intact nerve stimulated macrophage infiltration. We conclude that, following peripheral nerve injury, an immediate acute immune response occurs both distal and proximal to the lesion site and that the rapid transcriptional activation of the S100a8 and S100a9 genes results in S100A8/A9 hetero- and homodimers, which stimulate the release of chemokines and cytokines by activated Schwann cells and generate the initial chemotactic gradient that guides the transmigration of hematogenous immune cells into the injured nerve.
为了阐明切断的外周神经早期免疫反应过程,我们在大鼠坐骨神经切断模型中,对术后第1天的近端(P,再生)和远端(D,退化)神经残端进行了全基因组转录谱分析和生物信息学分析。在退化的D残端中,多个细胞死亡相关途径被激活,而在切断神经的P残端中,细胞骨架运动和糖异生/糖酵解途径的激活最为显著。我们的生物信息学分析还确定了趋化因子、白细胞介素、肿瘤坏死因子、主要组织相容性复合体、免疫球蛋白结合Fc受体、钙结合S100、基质金属蛋白酶、金属蛋白酶组织抑制剂和离子通道家族中,在P和D段均受影响的特定免疫调节基因。S100a8和S100a9是P和D段中上调最明显的基因。使用纯化的S100A8/A9异二聚体刺激培养的雪旺细胞,重现了我们最初在受伤神经中观察到的髓样细胞和吞噬细胞趋化基因及途径的激活。将S100A8/A9异二聚体注射到完整神经中会刺激巨噬细胞浸润。我们得出结论,外周神经损伤后,在损伤部位的远端和近端都会立即发生急性免疫反应,并且S100a8和S100a9基因的快速转录激活会产生S100A8/A9异二聚体和同二聚体,它们刺激活化的雪旺细胞释放趋化因子和细胞因子,并产生初始趋化梯度,引导造血免疫细胞迁移到受伤神经中。