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内体膜上的磷脂酰肌醇 4-磷酸和磷脂酰肌醇 4,5-二磷酸分离到不同的微域中。

Segregation of phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate into distinct microdomains on the endosome membrane.

机构信息

Field of Veterinary Pathobiology, Basic Veterinary Science, Department of Veterinary Medicine, Joint Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima 890-0065, Japan.

Medical Research Institute, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan.

出版信息

Biochim Biophys Acta Biomembr. 2017 Oct;1859(10):1880-1890. doi: 10.1016/j.bbamem.2017.06.014. Epub 2017 Jun 23.

Abstract

Phosphatidylinositol 4-phosphate (PtdIns(4)P) is the immediate precursor of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P), which is located on the cytoplasmic leaflet of the plasma membrane and has been reported to possess multiple cellular functions. Although PtdIns(4)P and PtdIns(4,5)P have been reported to localize to multiple intracellular compartments and to each function as regulatory molecules, their generation, regulation and functions in most intracellular compartments are not well-defined. To analyze PtdIns(4)P and PtdIns(4,5)P distributions, at a nanoscale, we employed an electron microscopy technique that specifically labels PtdIns(4)P and PtdIns(4,5)P on the freeze-fracture replica of intracellular biological membranes. This method minimizes the possibility of artificial perturbation, because molecules in the membrane are physically immobilized in situ. Using this technique, we found that PtdIns(4)P was localized to the cytoplasmic leaflet of Golgi apparatus and vesicular-shaped structures. The PtdIns(4,5)P labeling was observed in the cytoplasmic leaflet of the mitochondrial inner membrane and vesicular-shaped structures. Double labeling of PtdIns(4)P and PtdIns(4,5)P with endosome markers illustrated that PtdIns(4)P and PtdIns(4,5)P were mainly localized to the late endosome/lysosome and early endosome, respectively. PtdIns(4)P and PtdIns(4,5)P were colocalized in some endosomes, with the two phospholipids separated into distinct microdomains on the same endosomes. This is the first report showing, at a nanoscale, segregation of PtdIns(4)P- and PtdIns(4,5)P-enriched microdomains in the endosome, of likely importance for endosome functionality.

摘要

磷脂酰肌醇 4-磷酸(PtdIns(4)P)是磷脂酰肌醇 4,5-二磷酸(PtdIns(4,5)P)的直接前体,位于质膜的细胞质小叶中,据报道具有多种细胞功能。尽管已经报道 PtdIns(4)P 和 PtdIns(4,5)P 定位于多个细胞内隔室,并各自作为调节分子发挥作用,但它们在大多数细胞内隔室中的产生、调节和功能尚不清楚。为了在纳米尺度上分析 PtdIns(4)P 和 PtdIns(4,5)P 的分布,我们采用了一种电子显微镜技术,该技术专门标记细胞内生物膜的冷冻断裂复制品中的 PtdIns(4)P 和 PtdIns(4,5)P。这种方法最大限度地减少了人为干扰的可能性,因为膜中的分子在原位被物理固定。使用该技术,我们发现 PtdIns(4)P 定位于高尔基体和囊泡状结构的细胞质小叶。PtdIns(4,5)P 的标记出现在线粒体内膜的细胞质小叶和囊泡状结构中。用内体标记物对 PtdIns(4)P 和 PtdIns(4,5)P 进行双重标记表明,PtdIns(4)P 和 PtdIns(4,5)P 主要定位于晚期内体/溶酶体和早期内体。PtdIns(4)P 和 PtdIns(4,5)P 在一些内体中发生共定位,两种磷脂在同一内体上分离成不同的微区。这是首次在纳米尺度上显示内体中 PtdIns(4)P 和 PtdIns(4,5)P 富集微区的分离,这对内体功能可能很重要。

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