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含铅基因产物需要与Rab27a共同作用,将肌球蛋白Va募集到黑素细胞的黑素小体中。

The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes.

作者信息

Hume Alistair N, Collinson Lucy M, Hopkins Colin R, Strom Molly, Barral Duarte C, Bossi Giovanna, Griffiths Gillian M, Seabra Miguel C

机构信息

Cell and Molecular Biology, Division of Biomedical Sciences, Faculty of Medicine, Imperial College, London SW7 2AZ, UK.

出版信息

Traffic. 2002 Mar;3(3):193-202. doi: 10.1034/j.1600-0854.2002.030305.x.

Abstract

The function of lysosome-related organelles such as melanosomes in melanocytes, and lytic granules in cytotoxic T lymphocytes is disrupted in Griscelli syndrome and related diseases. Griscelli syndrome results from loss of function mutations in either the RAB27A (type 1 Griscelli syndrome) or MYO5A (type 2 Griscelli syndrome) genes. Melanocytes from Griscelli syndrome patients and respective murine models ashen (Rab27a mutant), dilute (myosin Va mutant), and leaden exhibit perinuclear clustering of melanosomes. Recent work suggests that Rab27a is required to recruit myosin Va to melanosomes, thereby tethering melanosomes to the peripheral actin network and promoting melanosome retention at the tips of melanocytic dendrites. Here, we characterize the function of the leaden gene product. We show that Rab27a, but not myosin Va, can be localized to melanosomes in leaden melanocytes, suggesting that the leaden gene product acts downstream of, or in parallel to, Rab27a in melanocytes to promote recruitment of myosin Va to melanosomes. We also observed reduced levels of myosin Va protein in leaden and ashen melanocytes, suggesting that myosin Va stability is influenced by the leaden and ashen gene products. In leaden cytotoxic T lymphocytes, we observed that lytic granules polarize towards the immunological synapse and kill target cells normally. However, in contrast to melanocytes, we found that neither the leaden gene product (melanophilin) nor myosin Va was detectable in cytotoxic T lymphocytes. These results suggest that Rab27a interacts with different classes of effector proteins in melanocytes and cytotoxic T lymphocytes.

摘要

在格里斯切利综合征及相关疾病中,黑素细胞中的黑素体以及细胞毒性T淋巴细胞中的溶细胞颗粒等溶酶体相关细胞器的功能会被破坏。格里斯切利综合征是由RAB27A基因(1型格里斯切利综合征)或MYO5A基因(2型格里斯切利综合征)功能丧失性突变引起的。来自格里斯切利综合征患者以及相应小鼠模型(灰鼠(Rab27a突变体)、淡化鼠(肌球蛋白Va突变体)和铅灰鼠)的黑素细胞表现出黑素体的核周聚集。最近的研究表明,Rab27a是将肌球蛋白Va招募到黑素体所必需的,从而将黑素体拴系到外周肌动蛋白网络,并促进黑素体保留在黑素细胞树突的末端。在此,我们对铅灰基因产物的功能进行了表征。我们发现,在铅灰黑素细胞中,Rab27a而非肌球蛋白Va能够定位于黑素体,这表明铅灰基因产物在黑素细胞中作用于Rab27a的下游或与之平行,以促进肌球蛋白Va向黑素体的招募。我们还观察到铅灰和灰鼠黑素细胞中肌球蛋白Va蛋白水平降低,这表明肌球蛋白Va的稳定性受铅灰和灰鼠基因产物的影响。在铅灰细胞毒性T淋巴细胞中,我们观察到溶细胞颗粒向免疫突触极化并正常杀伤靶细胞。然而,与黑素细胞不同的是,我们发现在细胞毒性T淋巴细胞中检测不到铅灰基因产物(黑素亲和蛋白)和肌球蛋白Va。这些结果表明,Rab27a在黑素细胞和细胞毒性T淋巴细胞中与不同类别的效应蛋白相互作用。

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