Arneth Borros M
Institute of Laboratory Medicine and Pathobiochemistry, Molecular Diagnostics, University Hospital of the Universities of Giessen and Marburg UKGM, Justus Liebig University Giessen, Giessen, Hessen, Germany.
PeerJ. 2018 Mar 9;6:e4462. doi: 10.7717/peerj.4462. eCollection 2018.
This study assessed in detail the influence of four different human proteins on the activation of CD4+ and CD8+ T lymphocytes and on the formation of regulatory T cells. Human whole-blood samples were incubated with four different human proteins. The effects of these proteins on the downstream immune-system response, on the expression of extracellular activation markers on and intracellular cytokines in T lymphocytes, and on the number of regulatory T cells (T-reg cells) were investigated via flow cytometry. Incubation with β-actin or glyceraldehyde 3-phosphate dehydrogenase (GAPDH), which are cytoplasmic proteins, increased the expression of both extracellular activation markers (CD69 and HLA-DR) and intracellular cytokines but did not significantly affect the number of T-reg cells. In contrast, incubation with human albumin or insulin, which are serum proteins, reduced both extracellular activation markers and intracellular cytokine expression and subsequently increased the number of T-reg cells. These findings may help to explain the etiological basis of autoimmune diseases.
本研究详细评估了四种不同人类蛋白质对CD4+和CD8+ T淋巴细胞活化以及调节性T细胞形成的影响。将人类全血样本与四种不同的人类蛋白质一起孵育。通过流式细胞术研究了这些蛋白质对下游免疫系统反应、T淋巴细胞细胞外活化标志物表达和细胞内细胞因子以及调节性T细胞(Treg细胞)数量的影响。与作为细胞质蛋白的β-肌动蛋白或甘油醛-3-磷酸脱氢酶(GAPDH)孵育,可增加细胞外活化标志物(CD69和HLA-DR)和细胞内细胞因子的表达,但对Treg细胞数量没有显著影响。相比之下,与作为血清蛋白的人白蛋白或胰岛素孵育,则会降低细胞外活化标志物和细胞内细胞因子的表达,并随后增加Treg细胞的数量。这些发现可能有助于解释自身免疫性疾病的病因基础。