Connor Ryan, Jones Letitia D, Qiu Xing, Thakar Juilee, Maggirwar Sanjay B
Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York, USA.
Department of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, New York, USA.
J Leukoc Biol. 2017 Oct;102(4):953-964. doi: 10.1189/jlb.6HI0217-043R. Epub 2017 Jun 29.
Leukocyte extravasation is a crucial feature of the normal immune response to disease and infection and is implicated in various pathologies during chronic inflammatory disease. P-Selectin glycoprotein ligand-1 (PSGL-1) is critical for leukocyte extravasation; however, despite extensive study, it remains unclear how its expression is regulated, which in turn, impedes a more precise understanding of how its expression level affects transmigration. To investigate the regulation of PSGL-1, 60 subjects, with or without HIV infection, were recruited and PSGL-1 expression in monocytes was measured. PSGL-1 was found to be up-regulated on leukocytes from HIV-infected individuals, and the physiologically relevant mediators soluble CD40 ligand (sCD40L) and glutamate were able to induce PSGL-1 transcription in human monocytes ex vivo. HIV-1 induced PSGL-1 induction, and its dependence on CD40L was validated further by use of the mouse-tropic HIV (EcoHIV) mouse model of HIV infection in C57BL/6 and CD40L knockout (KO) mice. To investigate crosstalk between the signaling cascades induced by CD40L and glutamate that lead to PSGL-1 induction, a network-based, discrete dynamic model was developed. The model reveals the MAPK pathway and oxidative stress as critical mediators of crosstalk between CD40L and glutamate-induced pathways. Importantly, the model predicted induction of the c-Myc transcription factor upon cotreatment, which was validated using transcriptomic data and pharmacologic inhibition of c-Myc. This study suggests a novel systems serology approach for translational research and reveals a mechanism for PSGL-1 transcriptional regulation, which might be leveraged to identify novel targets for therapeutic intervention.
白细胞外渗是机体对疾病和感染正常免疫反应的关键特征,并且在慢性炎症性疾病的各种病理过程中发挥作用。P-选择素糖蛋白配体-1(PSGL-1)对白细胞外渗至关重要;然而,尽管进行了广泛研究,其表达如何调控仍不清楚,这反过来又阻碍了我们更精确地理解其表达水平如何影响迁移。为了研究PSGL-1的调控机制,招募了60名有或无HIV感染的受试者,并检测了单核细胞中PSGL-1的表达。结果发现,HIV感染个体白细胞上的PSGL-1上调,生理相关介质可溶性CD40配体(sCD40L)和谷氨酸能够在体外诱导人单核细胞中PSGL-1的转录。HIV-1诱导了PSGL-1的上调,并且通过在C57BL/6和CD40L基因敲除(KO)小鼠中使用嗜鼠型HIV(EcoHIV)小鼠HIV感染模型进一步验证了其对CD40L的依赖性。为了研究由CD40L和谷氨酸诱导导致PSGL-1上调的信号级联之间的相互作用,构建了一个基于网络的离散动态模型。该模型揭示丝裂原活化蛋白激酶(MAPK)途径和氧化应激是CD40L和谷氨酸诱导途径之间相互作用的关键介质。重要的是,该模型预测联合处理会诱导c-Myc转录因子,这通过转录组数据和c-Myc的药理学抑制得到了验证。这项研究提出了一种用于转化研究的新型系统血清学方法,并揭示了PSGL-1转录调控的机制,这可能有助于确定治疗干预的新靶点。