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9-cis-Retinoic Acid Promotes Cell Adhesion Through Integrin Dependent and Independent Mechanisms Across Immune Lineages

机译:通过整合素依赖性和跨免疫谱系的独立机制促进细胞粘附促进细胞粘附

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摘要

Retinoids are essential in the proper establishment and maintenance of immunity. Although retinoids are implicated in immune related processes, their role in immune cell adhesion has not been well established. In this study, the effect of 9-cis-retinoic acid (9-cis-RA) on human hematopoietic cell adhesion was investigated. 9-cis-RA treatment specifically induced cell adhesion of the human immune cell lines HuT-78, NB4, RPMI 8866, and U937. Due to the prominent role of integrin receptors in mediating immune cell adhesion, we sought to evaluate if cell adhesion was integrin-dependent. By employing a variety of integrin antagonist including function-blocking antibodies and EDTA, we establish that 9-cis-RA prompts immune cell adhesion through established integrin receptors in addition to a novel integrin-independent process. The novel integrin-independent adhesion required the presence of retinoid and was attenuated by treatment with synthetic corticosteroids. Finally, we demonstrate that 9-cis-RA treatment of primary murine B-cells induces ex vivo adhesion that persists in the absence of integrin function. Our study is the first to demonstrate that 9-cis-retinoic acid influences immune cell adhesion through at least two functionally distinct mechanisms.
机译:类维生素A对于正确建立和维持免疫力至关重要。尽管类维生素A与免疫相关过程有关,但它们在免疫细胞粘附中的作用尚未很好地建立。在这项研究中,研究了9-顺-视黄酸(9-顺-RA)对人类造血细胞粘附的影响。 9-顺式-RA治疗可特异性诱导人免疫细胞HuT-78,NB4,RPMI 8866和U937的细胞粘附。由于整合素受体在介导免疫细胞黏附中的重要作用,我们试图评估细胞黏附是否依赖于整合素。通过采用包括功能阻断抗体和EDTA在内的各种整合素拮抗剂,我们确定9-顺式-RA通过新型整合素非依赖性过程,通过建立的整合素受体促进免疫细胞粘附。新型的不依赖整合素的粘附需要存在类维生素A,并通过合成皮质类固醇激素的治疗​​而减弱。最后,我们证明了9-顺式RA治疗原代鼠B细胞可诱导离体粘附,这种粘附在没有整联蛋白功能的情况下仍然存在。我们的研究首次证明9-顺-视黄酸通过至少两种功能上不同的机制影响免疫细胞粘附。

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