Rodriguez Paulo C, Ochoa Augusto C, Al-Khami Amir A
Augusta University, Georgia Cancer Center , Augusta, GA , USA.
Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, USA; Department of Pediatrics, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Front Immunol. 2017 Feb 7;8:93. doi: 10.3389/fimmu.2017.00093. eCollection 2017.
Arginine metabolism has been a key catabolic and anabolic process throughout the evolution of the immune response. Accruing evidence indicates that arginine-catabolizing enzymes, mainly nitric oxide synthases and arginases, are closely integrated with the control of immune response under physiological and pathological conditions. Myeloid cells are major players that exploit the regulators of arginine metabolism to mediate diverse, although often opposing, immunological and functional consequences. In this article, we focus on the importance of arginine catabolism by myeloid cells in regulating innate and adaptive immunity. Revisiting this matter could result in novel therapeutic approaches by which the immunoregulatory nodes instructed by arginine metabolism can be targeted.
在免疫反应的整个进化过程中,精氨酸代谢一直是关键的分解代谢和合成代谢过程。越来越多的证据表明,主要是一氧化氮合酶和精氨酸酶的精氨酸分解酶,在生理和病理条件下与免疫反应的控制密切相关。髓系细胞是利用精氨酸代谢调节因子来介导多种(尽管常常是相反的)免疫和功能后果的主要参与者。在本文中,我们重点关注髓系细胞的精氨酸分解代谢在调节固有免疫和适应性免疫中的重要性。重新审视这个问题可能会产生新的治疗方法,通过这些方法可以靶向由精氨酸代谢指示的免疫调节节点。