分类(Nexin-13)对内溶酶体胆固醇输出的新见解。

Albert Lu
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摘要

进出内溶酶体室的运输是调节细胞胆固醇稳态的关键步骤。尽管最近取得了重要的进展,但低密度脂蛋白衍生的游离胆固醇如何从内溶酶体的管腔输出到其他细胞器仍然是一个有争议的问题。我们最近设计了一种CRISPR/Cas9基因组规模的策略来发现参与调节内溶酶体胆固醇稳态和功能相关磷脂磷酸单酰基甘油的基因。这种方法证实了参与这一过程的已知基因和途径,更重要的是揭示了以前未被认识到的新参与者的作用,如分类Nexin-13 (SNX13)。在这里,我们讨论SNX13在内溶酶体胆固醇输出中的意想不到的调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sorting (Nexin-13) out Novel Insights into Endolysosomal Cholesterol Export.

Transport in and out of the endolysosomal compartment represents a key step in the regulation of cellular cholesterol homeostasis. Despite important recent advances, how LDL-derived, free cholesterol is exported from the lumen of endolysosomes to other organelles is still a matter of debate. We recently devised a CRISPR/Cas9 genome-scale strategy to uncover genes involved in the regulation of endolysosomal cholesterol homeostasis and the functionally linked phospholipid, bis(monoacylglycerol)-phosphate. This approach confirmed known genes and pathways involved in this process, and more importantly revealed previously unrecognized roles for new players, such as Sorting Nexin-13 (SNX13). Here we discuss the unexpected regulatory role of SNX13 in endolysosomal cholesterol export.

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