Taha Safa, Fathallah Mohamed Dahmani, Bakhiet Moiz
Department of Molecular Medicine, Princess Al-Jawhara Center for Genetics and Inherited Diseases, Arabian Gulf University, Manama 26671, Bahrain.
Biotechnology Program, College of Graduate Studies, Arabian Gulf University, Manama 26671, Bahrain.
Mol Med Rep. 2014 Jul;10(1):75-81. doi: 10.3892/mmr.2014.2225. Epub 2014 May 8.
We have recently described an immune system-released activating agent (ISRAA) as a nervous system-induced factor that stimulates immune responses in the mouse spleen. However, the human ISRAA has not yet been identified. In this study, we examined the effects of the mouse ISRAA protein on human peripheral blood mononuclear cells (PBMCs), to observe if the biological activity of this molecule is consistent between the two different species. Mouse ISRAA demonstrated dose-dependent dualistic effects on human cells, as 5 µg exhibited positive apoptosis and 50 pg exhibited significant proliferation (P<0.05). Furthermore, immunosuppressed cells from patients undergoing immunosuppressive therapy demonstrated significant proliferation to 50 pg ISRAA (P<0.05). Studies to compare sequences in different species revealed a preserved motif, exhibiting 72% similarity with the interspecies conserved signal peptide motif of tumor necrosis factor receptor 1 (TNFR1). A mutant ISRAA lacking this motif was produced and tested for its biological effects. The mutant ISRAA demonstrated neither apoptotic nor proliferative effects compared with wild type. Therefore, an interspecies conserved domain of ISRAA constitutes the active site of the molecule, and its effects on immunocompromised cells should be investigated for future therapies in the treatment of immunosuppressive disorders.
我们最近将一种免疫系统释放的激活剂(ISRAA)描述为一种由神经系统诱导的因子,它能刺激小鼠脾脏中的免疫反应。然而,人类ISRAA尚未被鉴定出来。在本研究中,我们检测了小鼠ISRAA蛋白对人外周血单个核细胞(PBMC)的影响,以观察该分子在两种不同物种间的生物活性是否一致。小鼠ISRAA对人细胞表现出剂量依赖性的双重作用,5微克时表现出阳性凋亡作用,50皮克时表现出显著增殖(P<0.05)。此外,接受免疫抑制治疗患者的免疫抑制细胞对50皮克ISRAA表现出显著增殖(P<0.05)。比较不同物种序列的研究揭示了一个保守基序,与肿瘤坏死因子受体1(TNFR1)的种间保守信号肽基序具有72%的相似性。制备了一个缺乏该基序的突变型ISRAA并检测其生物学效应。与野生型相比,突变型ISRAA既无凋亡作用也无增殖作用。因此,ISRAA的种间保守结构域构成了该分子的活性位点,其对免疫受损细胞的作用应在未来治疗免疫抑制性疾病的疗法中加以研究。