心理压力对自然杀伤细胞功能的影响:基于压力类型、持续时间、强度和物种的综合分析

IF 2.4 3区 医学 Q2 BEHAVIORAL SCIENCES
Alexis R. Katz , Margaret P. Huntwork , Jay K. Kolls , Jenny L. Hewes , Calder R. Ellsworth , Robert D.E. Clark , John C. Carlson
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引用次数: 0

摘要

自然杀伤细胞(NK)缺乏或功能障碍患者更容易受到疱疹病毒感染、疱疹病毒相关癌症和巨噬细胞活化综合征的影响。本综述总结了有关心理应激后 NK 细胞功能障碍的研究,重点关注应激源类型、持续时间、暴露年龄和研究物种。心理应激会对不同物种的 NK 细胞活性(NKCA)产生负面影响。长期的压力会导致 NK 细胞数量和功能的显著下降,而康复努力被证明无法有效逆转这些影响。由于 NKCA 功能受损,生命早期和长期的压力暴露尤其会增加感染和癌症的风险。综述还强调,压力对雄性和雌性的影响不同,雌性表现出更多的免疫抑制 NK 细胞表型。值得注意的是,小鼠的反应与人类和其他动物不同,因此不适合进行 NK 细胞应激相关研究。大多数研究使用针对 K-562 或 YAC-1 细胞的细胞溶解试验来测量 NKCA。虽然应激状态下 NK 细胞功能障碍的确切机制仍不清楚,但潜在的原因包括释放穿孔素或颗粒酶的分泌溶酶体减少、NK 细胞突触形成受损、CD2 或 LFA-1 (CD11a) 等突触相关分子表达减少、活化受体表达改变以及信号通路失调,如 Erk1/2 磷酸化和 NFkB 信号减少。这些机制并不相互排斥,未来的研究需要明确这些途径,并开发出针对应激诱导的免疫失调的治疗干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of psychological stressors on natural killer cell function: A comprehensive analysis based on stressor type, duration, intensity, and species
Patients with natural killer (NK) cell deficiency or dysfunction are more susceptible to infections by Herpesviridae viruses, herpesvirus-related cancers, and macrophage activation syndromes. This review summarizes research on NK cell dysfunction following psychological stress, focusing on stressor type, duration, age of exposure, and species studied. Psychological stressors negatively affect NK cell activity (NKCA) across species. Prolonged stress leads to more significant decreases in NK cell number and function, with rehabilitation efforts proving ineffective in reversing these effects. Early life and prolonged stress exposure particularly increases the risk of infections and cancer due to impaired NKCA. The review also highlights that stress impacts males and females differently, with females exhibiting a more immunosuppressed NK cell phenotype. Notably, mice respond differently compared to humans and other animals, making them unsuitable for NK cell stress-related studies. Most studies measured NKCA using cytolytic assays against K-562 or YAC-1 cells. Although the exact mechanisms of NK cell dysfunction under stress remain unclear, potential causes include reduced release of secretory lysosomes with perforin or granzyme, impaired NK cell synapse formation, decreased expression of synapse-related molecules like CD2 or LFA-1 (CD11a), altered activating receptor expression, and dysregulated signaling pathways, such as decreased Erk1/2 phosphorylation and NFkB signaling.
These mechanisms are not mutually exclusive, and future research is needed to clarify these pathways and develop therapeutic interventions for stress-induced immune dysregulation.
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来源期刊
Physiology & Behavior
Physiology & Behavior 医学-行为科学
CiteScore
5.70
自引率
3.40%
发文量
274
审稿时长
47 days
期刊介绍: Physiology & Behavior is aimed at the causal physiological mechanisms of behavior and its modulation by environmental factors. The journal invites original reports in the broad area of behavioral and cognitive neuroscience, in which at least one variable is physiological and the primary emphasis and theoretical context are behavioral. The range of subjects includes behavioral neuroendocrinology, psychoneuroimmunology, learning and memory, ingestion, social behavior, and studies related to the mechanisms of psychopathology. Contemporary reviews and theoretical articles are welcomed and the Editors invite such proposals from interested authors.
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