HIV Immunopathogenesis Laboratory, The Wistar Institute, Philadelphia, PA.
Proteomics and Metabolomics Facility, The Wistar Institute, Philadelphia, PA.
J Acquir Immune Defic Syndr. 2019 Feb 1;80(2):234-241. doi: 10.1097/QAI.0000000000001911.
HIV-exposed seronegative people who inject drugs (HESN-PWID) have been shown to have increased natural killer (NK) cell and myeloid activation when compared with control donors.
We investigated potential mechanisms maintaining NK activation by conducting quantitative proteome comparisons of NK cells from HESN-PWID subjects and control donors. Proteins upregulated in NK cells were measured in the plasma of HESN-PWID subjects by ELISA and further investigated for their ability to induce innate immune activation in vitro.
The NK cell proteome comparison showed markedly higher levels of interferon-stimulated proteins and S100 proteins, including S100A14. Consistent with these results, we observed significantly higher levels of S100A14 in the plasma of HESN-PWID subjects compared with controls (P = 0.033, n = 25). In vitro, the addition of recombinant S100A14 protein significantly activated NK cells in a peripheral blood mononuclear cell mixture (P = 0.011, n = 9), but not purified NK cells alone. Treatment of purified monocytes with recombinant S100A14 protein induced secretion of TNF-alpha and led to significantly higher NK CD69 activation (P = 0.0156, n = 7) in a co-culture through a TLR4-dependent interaction.
Our study identified S100A14 as a novel protein increased within NK cells and plasma of HESN-PWID subjects with the capacity to sustain NK activation through TLR4-dependent activation of myeloid cells.
与对照供体相比,HIV 暴露但血清阴性的静脉注射吸毒者(HESN-PWID)的自然杀伤(NK)细胞和髓系激活明显增加。
我们通过对 HESN-PWID 受试者和对照供体的 NK 细胞进行定量蛋白质组比较,研究维持 NK 激活的潜在机制。通过 ELISA 测量 HESN-PWID 受试者 NK 细胞中上调的蛋白质,并进一步研究其在体外诱导固有免疫激活的能力。
NK 细胞蛋白质组比较显示干扰素刺激蛋白和 S100 蛋白(包括 S100A14)水平明显升高。与这些结果一致,我们观察到 HESN-PWID 受试者的血浆中 S100A14 水平明显高于对照组(P = 0.033,n = 25)。在体外,添加重组 S100A14 蛋白可显著激活外周血单核细胞混合物中的 NK 细胞(P = 0.011,n = 9),但不能单独激活纯化的 NK 细胞。用重组 S100A14 蛋白处理纯化的单核细胞可诱导 TNF-α的分泌,并通过 TLR4 依赖性相互作用导致共培养中 NK CD69 的激活显著增加(P = 0.0156,n = 7)。
我们的研究确定 S100A14 为一种新型蛋白,其在 HESN-PWID 受试者的 NK 细胞和血浆中增加,通过 TLR4 依赖性激活髓样细胞维持 NK 激活的能力。