• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

溶酶体酸性磷酸酶通过细胞表面被转运至溶酶体。

Lysosomal acid phosphatase is transported to lysosomes via the cell surface.

作者信息

Braun M, Waheed A, von Figura K

机构信息

Institut für Biochemie II, Göttingen, FRG.

出版信息

EMBO J. 1989 Dec 1;8(12):3633-40. doi: 10.1002/j.1460-2075.1989.tb08537.x.

DOI:10.1002/j.1460-2075.1989.tb08537.x
PMID:2583113
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC402045/
Abstract

Lysosomal acid phosphatase (LAP) is transported as a transmembrane protein to dense lysosomes. The pathway of LAP to lysosomes includes the passage through the plasma membrane. LAP is transported from the trans-Golgi to the cell surface with a half-time of less than 10 min. Cell surface LAP is rapidly internalized. Most of the internalized LAP is transported back to the cell surface. On average, each LAP molecule cycles greater than 15 times between the cell surface and the endosomes before it is transferred to dense lysosomes. At equilibrium approximately 4 times more LAP precursor is present in endosomes than at the cell surface. Exposing cells to reduced temperature or weak bases such as NH4Cl, chloroquine and primaquine decreases the steady-state concentration of LAP at the cell surface. The recycling pathway is operative at greater than or equal to 20 degrees C and does not include passage of the Golgi/trans-Golgi network. LAP is transferred with a half-time of 5-6 h from the plasma membrane/endosome pool to dense lysosomes, from where it does not recycle to the endosome/plasma membrane pool at a measurable rate.

摘要

溶酶体酸性磷酸酶(LAP)作为一种跨膜蛋白被转运至致密溶酶体。LAP至溶酶体的途径包括穿过质膜。LAP从反式高尔基体转运至细胞表面的半衰期不到10分钟。细胞表面的LAP会迅速内化。大部分内化的LAP会被转运回细胞表面。平均而言,每个LAP分子在被转运至致密溶酶体之前,会在细胞表面和内体之间循环超过15次。在平衡状态下,内体中存在的LAP前体比细胞表面大约多4倍。将细胞暴露于低温或弱碱如氯化铵、氯喹和伯氨喹会降低细胞表面LAP的稳态浓度。循环途径在大于或等于20摄氏度时起作用,且不包括高尔基体/反式高尔基体网络的通过。LAP从质膜/内体池转运至致密溶酶体的半衰期为5 - 6小时,从致密溶酶体它不会以可测量的速率再循环至内体/质膜池。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/089fb9c5fb69/emboj00136-0099-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/ffd748c10463/emboj00136-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/7af61221f5fb/emboj00136-0095-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/716ef9f53556/emboj00136-0095-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/1853dc522bc9/emboj00136-0095-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/fc21719d720e/emboj00136-0096-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/a341a04fc9b8/emboj00136-0097-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/1199032a44f3/emboj00136-0098-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/c07dc7f34f06/emboj00136-0098-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/b06db30eb361/emboj00136-0099-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/6ae2cb0b1f51/emboj00136-0099-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/089fb9c5fb69/emboj00136-0099-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/ffd748c10463/emboj00136-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/7af61221f5fb/emboj00136-0095-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/716ef9f53556/emboj00136-0095-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/1853dc522bc9/emboj00136-0095-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/fc21719d720e/emboj00136-0096-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/a341a04fc9b8/emboj00136-0097-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/1199032a44f3/emboj00136-0098-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/c07dc7f34f06/emboj00136-0098-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/b06db30eb361/emboj00136-0099-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/6ae2cb0b1f51/emboj00136-0099-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/610b/402045/089fb9c5fb69/emboj00136-0099-c.jpg

相似文献

1
Lysosomal acid phosphatase is transported to lysosomes via the cell surface.溶酶体酸性磷酸酶通过细胞表面被转运至溶酶体。
EMBO J. 1989 Dec 1;8(12):3633-40. doi: 10.1002/j.1460-2075.1989.tb08537.x.
2
The tyrosine motifs of Lamp 1 and LAP determine their direct and indirect targetting to lysosomes.Lamp 1和LAP的酪氨酸基序决定了它们直接和间接靶向溶酶体的方式。
J Cell Sci. 2002 Jan 1;115(Pt 1):185-94. doi: 10.1242/jcs.115.1.185.
3
Human lysosomal acid phosphatase is transported as a transmembrane protein to lysosomes in transfected baby hamster kidney cells.人溶酶体酸性磷酸酶作为一种跨膜蛋白被转运至转染的幼仓鼠肾细胞中的溶酶体。
EMBO J. 1988 Aug;7(8):2351-8. doi: 10.1002/j.1460-2075.1988.tb03079.x.
4
Targeting of a lysosomal membrane protein: a tyrosine-containing endocytosis signal in the cytoplasmic tail of lysosomal acid phosphatase is necessary and sufficient for targeting to lysosomes.溶酶体膜蛋白的靶向定位:溶酶体酸性磷酸酶胞质尾部含酪氨酸的内吞信号对于靶向溶酶体而言是必要且充分的。
EMBO J. 1990 Nov;9(11):3497-506. doi: 10.1002/j.1460-2075.1990.tb07558.x.
5
Cycling of two endogenous lysosomal membrane proteins, lamp-2 and acid phosphatase, between the cell surface and lysosomes in cultured rat hepatocytes.培养的大鼠肝细胞中两种内源性溶酶体膜蛋白(Lamp-2和酸性磷酸酶)在细胞表面和溶酶体之间的循环。
J Biochem. 1993 Oct;114(4):598-604. doi: 10.1093/oxfordjournals.jbchem.a124223.
6
The lysosomal membrane glycoprotein lamp-1 is transported to lysosomes by two alternative pathways.溶酶体膜糖蛋白lamp-1通过两条不同的途径转运至溶酶体。
Arch Biochem Biophys. 1992 Aug 1;296(2):630-9. doi: 10.1016/0003-9861(92)90619-8.
7
Sequential processing of lysosomal acid phosphatase by a cytoplasmic thiol proteinase and a lysosomal aspartyl proteinase.溶酶体酸性磷酸酶先后由一种胞质硫醇蛋白酶和一种溶酶体天冬氨酰蛋白酶进行加工处理。
EMBO J. 1989 Nov;8(11):3215-9. doi: 10.1002/j.1460-2075.1989.tb08480.x.
8
Kinetics of intracellular transport and sorting of lysosomal membrane and plasma membrane proteins.溶酶体膜蛋白和质膜蛋白的细胞内运输及分选动力学
J Cell Biol. 1987 Sep;105(3):1227-40. doi: 10.1083/jcb.105.3.1227.
9
Two lysosomal membrane proteins, LGP85 and LGP107, are delivered to late endosomes/lysosomes through different intracellular routes after exiting from the trans-Golgi network.两种溶酶体膜蛋白,LGP85和LGP107,从反式高尔基体网络排出后通过不同的细胞内途径被转运至晚期内体/溶酶体。
Biochem Biophys Res Commun. 2003 Feb 21;301(4):833-40. doi: 10.1016/s0006-291x(03)00046-9.
10
Transport of acid phosphatase to lysosomes does not involve passage through the cell surface.
Biochem Biophys Res Commun. 1990 Aug 16;170(3):1067-73. doi: 10.1016/0006-291x(90)90501-d.

引用本文的文献

1
The endolysosomal system in conventional and unconventional protein secretion.经典和非经典蛋白分泌途径中的内溶酶体系统。
J Cell Biol. 2024 Sep 2;223(9). doi: 10.1083/jcb.202404152. Epub 2024 Aug 12.
2
The role of the AP-1 adaptor complex in outgoing and incoming membrane traffic.AP-1 衔接复合物在外向和内吞膜运输中的作用。
J Cell Biol. 2024 Jul 1;223(7). doi: 10.1083/jcb.202310071. Epub 2024 Apr 5.
3
Lysosomal membrane proteins LAMP1 and LIMP2 are segregated in the Golgi apparatus independently of their clathrin adaptor binding motif.

本文引用的文献

1
Biosynthesis and transport of cathepsin D in cultured human fibroblasts.组织蛋白酶D在培养的人成纤维细胞中的生物合成与运输
J Cell Biol. 1983 Jul;97(1):1-5. doi: 10.1083/jcb.97.1.1.
2
Swainsonine inhibits the biosynthesis of complex glycoproteins by inhibition of Golgi mannosidase II.苦马豆素通过抑制高尔基体甘露糖苷酶II来抑制复合糖蛋白的生物合成。
J Biol Chem. 1982 Jul 25;257(14):7936-9.
3
Immunocytochemical localization of alpha-D-mannosidase II in the Golgi apparatus of rat liver.大鼠肝脏高尔基体中α-D-甘露糖苷酶II的免疫细胞化学定位
溶酶体膜蛋白LAMP1和LIMP2在高尔基体中分离,与它们的网格蛋白衔接蛋白结合基序无关。
Mol Biol Cell. 2024 Mar 1;35(3):ar42. doi: 10.1091/mbc.E23-06-0251. Epub 2024 Jan 17.
4
BORC-ARL8-HOPS ensemble is required for lysosomal cholesterol egress through NPC2.BORC-ARL8-HOPS 复合物通过 NPC2 对于溶酶体胆固醇外排是必需的。
Mol Biol Cell. 2022 Aug 1;33(9):ar81. doi: 10.1091/mbc.E21-11-0595-T. Epub 2022 Jun 2.
5
Is P-Glycoprotein Functionally Expressed in the Limiting Membrane of Endolysosomes? A Biochemical and Ultrastructural Study in the Rat Liver.P-糖蛋白在内涵体溶酶体的限制膜上是否有功能表达?大鼠肝的生化和超微结构研究。
Cells. 2022 May 5;11(9):1556. doi: 10.3390/cells11091556.
6
Loss of Christianson Syndrome Na/H Exchanger 6 (NHE6) Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons.丧失 Christianson 综合征 Na+/H+ 交换蛋白 6(NHE6)导致神经元溶酶体功能障碍的内体成熟和运输异常。
J Neurosci. 2021 Nov 3;41(44):9235-9256. doi: 10.1523/JNEUROSCI.1244-20.2021. Epub 2021 Sep 15.
7
A Review of Small Molecule Inhibitors and Functional Probes of Human Cathepsin L.人组织蛋白酶 L 的小分子抑制剂和功能探针研究综述
Molecules. 2020 Feb 6;25(3):698. doi: 10.3390/molecules25030698.
8
The phytochemical polydatin ameliorates non-alcoholic steatohepatitis by restoring lysosomal function and autophagic flux.原花青素通过恢复溶酶体功能和自噬流来改善非酒精性脂肪性肝炎。
J Cell Mol Med. 2019 Jun;23(6):4290-4300. doi: 10.1111/jcmm.14320. Epub 2019 Apr 11.
9
Segregation in the Golgi complex precedes export of endolysosomal proteins in distinct transport carriers.在内溶酶体蛋白通过不同的运输载体输出之前,它们会在高尔基体复合体中进行分选。
J Cell Biol. 2017 Dec 4;216(12):4141-4151. doi: 10.1083/jcb.201707172. Epub 2017 Oct 4.
10
Cytoplasmic tail of coronavirus spike protein has intracellular targeting signals.冠状病毒刺突蛋白的细胞质尾部具有细胞内靶向信号。
J Biosci. 2017 Jun;42(2):231-244. doi: 10.1007/s12038-017-9676-7.
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4364-8. doi: 10.1073/pnas.80.14.4364.
4
Antibody against the insulin receptor causes disappearance of insulin receptors in 3T3-L1 cells: a possible explanation of antibody-induced insulin resistance.抗胰岛素受体抗体导致3T3-L1细胞中胰岛素受体消失:抗体诱导胰岛素抵抗的一种可能解释。
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2508-11. doi: 10.1073/pnas.81.8.2508.
5
Properties of a monoclonal antibody to epidermal growth factor receptor with implications for the mechanism of action of EGF.一种针对表皮生长因子受体的单克隆抗体的特性及其对表皮生长因子作用机制的影响
EMBO J. 1984 May;3(5):929-37. doi: 10.1002/j.1460-2075.1984.tb01910.x.
6
Biosynthesis of the human asialoglycoprotein receptor.人去唾液酸糖蛋白受体的生物合成
J Biol Chem. 1983 Sep 25;258(18):11249-55.
7
Biosynthesis of the human transferrin receptor in cultured cells.培养细胞中人转铁蛋白受体的生物合成
J Biol Chem. 1981 Dec 25;256(24):12888-92.
8
Phase separation of integral membrane proteins in Triton X-114 solution.整合膜蛋白在Triton X-114溶液中的相分离。
J Biol Chem. 1981 Feb 25;256(4):1604-7.
9
Cathepsin D and beta-hexosaminidase synthesized in the presence of 1-deoxynojirimycin accumulate in the endoplasmic reticulum.在1-脱氧野尻霉素存在的情况下合成的组织蛋白酶D和β-己糖胺酶在内质网中积累。
J Biol Chem. 1984 Aug 25;259(16):10129-35.
10
Juvenile and adult metachromatic leukodystrophy: partial restoration of arylsulfatase A (cerebroside sulfatase) activity by inhibitors of thiol proteinases.青少年和成人异染性脑白质营养不良:巯基蛋白酶抑制剂对芳基硫酸酯酶A(脑苷脂硫酸酯酶)活性的部分恢复作用
Proc Natl Acad Sci U S A. 1983 Oct;80(19):6066-70. doi: 10.1073/pnas.80.19.6066.