• 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

基质金属蛋白酶1(Mmp1)和基质金属蛋白酶2(Mmp2)通过不同作用协同诱导果蝇脂肪体细胞解离。

Mmp1 and Mmp2 cooperatively induce Drosophila fat body cell dissociation with distinct roles.

作者信息

Jia Qiangqiang, Liu Yang, Liu Hanhan, Li Sheng

机构信息

Key Laboratory of Insect Developmental and Evolutionary Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.

出版信息

Sci Rep. 2014 Dec 18;4:7535. doi: 10.1038/srep07535.

DOI:10.1038/srep07535
PMID:25520167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4269897/
Abstract

During Drosophila metamorphosis, the single-cell layer of fat body tissues gradually dissociates into individual cells. Via a fat body-specific RNAi screen in this study, we found that two matrix metalloproteinases (MMPs), Mmp1 and Mmp2, are both required for fat body cell dissociation. As revealed through a series of cellular, biochemical, molecular, and genetic experiments, Mmp1 preferentially cleaves DE-cadherin-mediated cell-cell junctions, while Mmp2 preferentially degrades basement membrane (BM) components and thus destroy cell-BM junctions, resulting in the complete dissociation of the entire fat body tissues into individual cells. Moreover, several genetic interaction experiments demonstrated that the roles of Mmp1 and Mmp2 in this developmental process are cooperative. In conclusion, Mmp1 and Mmp2 induce fat body cell dissociation during Drosophila metamorphosis in a cooperative yet distinct manner, a finding that sheds light on the general mechanisms by which MMPs regulate tissue remodeling in animals.

摘要

在果蝇变态发育过程中,脂肪体组织的单细胞层逐渐解离为单个细胞。通过本研究中针对脂肪体的RNA干扰筛选,我们发现两种基质金属蛋白酶(MMPs),即Mmp1和Mmp2,对于脂肪体细胞解离都是必需的。通过一系列细胞、生化、分子和遗传学实验表明,Mmp1优先切割DE-钙黏蛋白介导的细胞间连接,而Mmp2优先降解基底膜(BM)成分,从而破坏细胞与BM的连接,导致整个脂肪体组织完全解离为单个细胞。此外,一些遗传相互作用实验表明,Mmp1和Mmp2在这个发育过程中的作用是协同的。总之,Mmp1和Mmp2以协同但不同的方式诱导果蝇变态发育过程中的脂肪体细胞解离,这一发现揭示了MMPs调节动物组织重塑的一般机制。

相似文献

1
Mmp1 and Mmp2 cooperatively induce Drosophila fat body cell dissociation with distinct roles.基质金属蛋白酶1(Mmp1)和基质金属蛋白酶2(Mmp2)通过不同作用协同诱导果蝇脂肪体细胞解离。
Sci Rep. 2014 Dec 18;4:7535. doi: 10.1038/srep07535.
2
Fear-of-intimacy-mediated zinc transport controls fat body cell dissociation through modulating Mmp activity in Drosophila.恐惧亲密关系介导的锌转运通过调节果蝇中 MMP 活性控制脂肪体细胞解离。
Cell Death Dis. 2021 Sep 25;12(10):874. doi: 10.1038/s41419-021-04147-z.
3
Matrix Metalloproteinases are required for membrane motility and lumenogenesis during Drosophila heart development.基质金属蛋白酶是果蝇心脏发育过程中膜运动和管腔形成所必需的。
PLoS One. 2017 Feb 13;12(2):e0171905. doi: 10.1371/journal.pone.0171905. eCollection 2017.
4
ßFTZ-F1 and Matrix metalloproteinase 2 are required for fat-body remodeling in Drosophila.ßFTZ-F1 和基质金属蛋白酶 2 对于果蝇体脂肪组织重构是必需的。
Dev Biol. 2011 Dec 15;360(2):286-96. doi: 10.1016/j.ydbio.2011.09.015. Epub 2011 Sep 22.
5
Matrix metalloproteinases promote fat body cell dissociation and ovary development in Bombyx mori.基质金属蛋白酶促进家蚕脂肪体细胞解离和卵巢发育。
J Insect Physiol. 2018 Nov-Dec;111:8-15. doi: 10.1016/j.jinsphys.2018.10.002. Epub 2018 Oct 6.
6
The expression, purification, and substrate analysis of matrix metalloproteinases in Drosophila melanogaster.果蝇中基质金属蛋白酶的表达、纯化和底物分析。
Protein Expr Purif. 2020 Jul;171:105629. doi: 10.1016/j.pep.2020.105629. Epub 2020 Mar 19.
7
Matrix metalloproteinases promote motor axon fasciculation in the Drosophila embryo.基质金属蛋白酶促进果蝇胚胎中的运动轴突成束。
Development. 2008 Jan;135(1):95-109. doi: 10.1242/dev.011072. Epub 2007 Nov 28.
8
Two classes of matrix metalloproteinases reciprocally regulate synaptogenesis.两类基质金属蛋白酶相互调节突触形成。
Development. 2016 Jan 1;143(1):75-87. doi: 10.1242/dev.124461. Epub 2015 Nov 24.
9
Loss of SPARC dysregulates basal lamina assembly to disrupt larval fat body homeostasis in Drosophila melanogaster.在黑腹果蝇中,富含半胱氨酸的酸性分泌蛋白(SPARC)的缺失会失调基膜组装,从而破坏幼虫脂肪体的稳态。
Dev Dyn. 2015 Apr;244(4):540-52. doi: 10.1002/dvdy.24243. Epub 2015 Jan 24.
10
Matrix metalloproteinases regulate ECM accumulation but not larval heart growth in Drosophila melanogaster.基质金属蛋白酶调节细胞外基质的积累,但不调节果蝇幼虫心脏的生长。
J Mol Cell Cardiol. 2020 Mar;140:42-55. doi: 10.1016/j.yjmcc.2020.02.008. Epub 2020 Feb 24.

引用本文的文献

1
Multi-Omic Analysis Identifies Key Genes Driving Testicular Fusion in .多组学分析确定了驱动……睾丸融合的关键基因。 (原文句末不完整)
Int J Mol Sci. 2025 Jun 10;26(12):5564. doi: 10.3390/ijms26125564.
2
Macrophage invasion into the Drosophila brain requires JAK/STAT-dependent MMP activation in the blood-brain barrier.巨噬细胞侵入果蝇大脑需要血脑屏障中依赖JAK/STAT的基质金属蛋白酶激活。
PLoS Biol. 2025 Feb 20;23(2):e3003035. doi: 10.1371/journal.pbio.3003035. eCollection 2025 Feb.
3
A tumor-secreted protein utilizes glucagon release to cause host wasting.

本文引用的文献

1
E93 predominantly transduces 20-hydroxyecdysone signaling to induce autophagy and caspase activity in Drosophila fat body.E93 主要将 20-羟基蜕皮激素信号转导到果蝇脂肪体中,以诱导自噬和半胱天冬酶活性。
Insect Biochem Mol Biol. 2014 Feb;45:30-9. doi: 10.1016/j.ibmb.2013.11.005. Epub 2013 Dec 4.
2
Balancing crosstalk between 20-hydroxyecdysone-induced autophagy and caspase activity in the fat body during Drosophila larval-prepupal transition.在果蝇幼虫向预蛹期过渡期间,平衡 20-羟基蜕皮酮诱导的自噬和半胱天冬酶活性之间的串扰。
Insect Biochem Mol Biol. 2013 Nov;43(11):1068-78. doi: 10.1016/j.ibmb.2013.09.001. Epub 2013 Sep 12.
3
一种肿瘤分泌蛋白利用胰高血糖素释放导致宿主消瘦。
Cell Discov. 2025 Feb 10;11(1):11. doi: 10.1038/s41421-024-00762-0.
4
Improved whole-mount immunofluorescence protocol for consistent and robust labeling of adult Drosophila melanogaster adipose tissue.改良的成年黑腹果蝇脂肪组织整体免疫荧光标记协议,以获得一致且稳健的标记效果。
Biol Open. 2024 Aug 15;13(8). doi: 10.1242/bio.060491. Epub 2024 Aug 1.
5
Improving dermal fibroblast-to-epidermis communications and aging wound repair through extracellular vesicle-mediated delivery of Gstm2 mRNA.通过外泌体介导的 Gstm2 mRNA 递送来改善真皮成纤维细胞与表皮的通讯和老化伤口修复。
J Nanobiotechnology. 2024 Jun 2;22(1):307. doi: 10.1186/s12951-024-02541-1.
6
Proteomic Analysis of the Midgut Contents of Silkworm in the Pupal Stage.家蚕蛹期肠道内容物的蛋白质组学分析
Insects. 2023 Dec 15;14(12):953. doi: 10.3390/insects14120953.
7
Finishing the egg.吃完鸡蛋。
Genetics. 2024 Jan 3;226(1). doi: 10.1093/genetics/iyad183.
8
MicroRNA miR-263b-5p Regulates Developmental Growth and Cell Association by Suppressing in .微小RNA miR-263b-5p通过抑制……中的……来调节发育生长和细胞黏附。 (注:原文部分内容缺失,导致译文不太完整准确)
Biology (Basel). 2023 Aug 7;12(8):1096. doi: 10.3390/biology12081096.
9
Ectopic expression of matrix metalloproteinases and filopodia extension via JNK activation are involved in the invasion of blood tumor cells in Drosophila mxc mutant.基质金属蛋白酶和丝状伪足的异位表达通过 JNK 激活参与了果蝇 mxc 突变体中血液肿瘤细胞的入侵。
Genes Cells. 2023 Oct;28(10):709-726. doi: 10.1111/gtc.13060. Epub 2023 Aug 24.
10
Sterol Regulation of Development and 20-Hydroxyecdysone Biosynthetic and Signaling Genes in .固醇对 发育和 20-羟蜕皮甾酮生物合成及信号基因的调控
Cells. 2023 Jun 28;12(13):1739. doi: 10.3390/cells12131739.
PKC-mediated USP phosphorylation at Ser35 modulates 20-hydroxyecdysone signaling in Drosophila.
蛋白激酶 C 介导的丝氨酸 35 位 USP 磷酸化调节果蝇中的 20-羟基蜕皮酮信号。
J Proteome Res. 2012 Dec 7;11(12):6187-96. doi: 10.1021/pr3008804. Epub 2012 Nov 16.
4
Requirement of matrix metalloproteinase-1 for intestinal homeostasis in the adult Drosophila midgut.基质金属蛋白酶-1在成年果蝇中肠内稳态中的需求。
Exp Cell Res. 2012 Mar 10;318(5):670-81. doi: 10.1016/j.yexcr.2012.01.004. Epub 2012 Jan 12.
5
A secreted MMP is required for reepithelialization during wound healing.在伤口愈合过程中,一种分泌型 MMP 对于再上皮化是必需的。
Mol Biol Cell. 2012 Mar;23(6):1068-79. doi: 10.1091/mbc.E11-09-0745. Epub 2012 Jan 19.
6
ßFTZ-F1 and Matrix metalloproteinase 2 are required for fat-body remodeling in Drosophila.ßFTZ-F1 和基质金属蛋白酶 2 对于果蝇体脂肪组织重构是必需的。
Dev Biol. 2011 Dec 15;360(2):286-96. doi: 10.1016/j.ydbio.2011.09.015. Epub 2011 Sep 22.
7
Shaping cells and organs in Drosophila by opposing roles of fat body-secreted Collagen IV and perlecan.在果蝇中通过脂肪体分泌的胶原 IV 和 perlecan 的拮抗作用来塑造细胞和器官。
Dev Cell. 2011 Aug 16;21(2):245-56. doi: 10.1016/j.devcel.2011.06.026.
8
Integrins are necessary for the development and maintenance of the glial layers in the Drosophila peripheral nerve.整联蛋白对于果蝇外周神经中神经胶质层的发育和维持是必需的。
Development. 2011 Sep;138(17):3813-22. doi: 10.1242/dev.064816.
9
MMP20 cleaves E-cadherin and influences ameloblast development.MMP20 酶切 E-钙黏蛋白并影响成釉细胞发育。
Cells Tissues Organs. 2011;194(2-4):222-6. doi: 10.1159/000324205. Epub 2011 Apr 28.
10
Juvenile hormone counteracts the bHLH-PAS transcription factors MET and GCE to prevent caspase-dependent programmed cell death in Drosophila.保幼激素可拮抗bHLH-PAS转录因子MET和GCE,以防止果蝇中依赖半胱天冬酶的程序性细胞死亡。
Development. 2009 Jun;136(12):2015-25. doi: 10.1242/dev.033712.