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1
Specific activation of p85-p110 phosphatidylinositol 3'-kinase stimulates DNA synthesis by ras- and p70 S6 kinase-dependent pathways.p85-p110磷脂酰肌醇3'-激酶的特异性激活通过ras和p70 S6激酶依赖性途径刺激DNA合成。
Mol Cell Biol. 1997 Jan;17(1):248-55. doi: 10.1128/MCB.17.1.248.
2
Interactive roles of Ras, insulin receptor substrate-1, and proteins with Src homology-2 domains in insulin signaling in Xenopus oocytes.Ras、胰岛素受体底物-1以及具有Src同源结构域2的蛋白质在非洲爪蟾卵母细胞胰岛素信号传导中的相互作用
J Biol Chem. 1994 Nov 4;269(44):27645-9.
3
Activation of phosphatidylinositol 3-kinase, protein kinase B, and p70 S6 kinases in lipopolysaccharide-stimulated Raw 264.7 cells: differential effects of rapamycin, Ly294002, and wortmannin on nitric oxide production.脂多糖刺激的Raw 264.7细胞中磷脂酰肌醇3激酶、蛋白激酶B和p70 S6激酶的激活:雷帕霉素、Ly294002和渥曼青霉素对一氧化氮产生的不同影响。
J Immunol. 1998 Dec 15;161(12):6947-54.
4
A regulatory role for cAMP in phosphatidylinositol 3-kinase/p70 ribosomal S6 kinase-mediated DNA synthesis in platelet-derived-growth-factor-stimulated bovine airway smooth-muscle cells.环磷酸腺苷(cAMP)在血小板衍生生长因子刺激的牛气道平滑肌细胞中对磷脂酰肌醇3激酶/p70核糖体S6激酶介导的DNA合成的调节作用。
Biochem J. 1996 Sep 15;318 ( Pt 3)(Pt 3):965-71. doi: 10.1042/bj3180965.
5
Insulin stimulation of glycogen synthesis and glycogen synthase activity is blocked by wortmannin and rapamycin in 3T3-L1 adipocytes: evidence for the involvement of phosphoinositide 3-kinase and p70 ribosomal protein-S6 kinase.渥曼青霉素和雷帕霉素可阻断3T3-L1脂肪细胞中胰岛素对糖原合成及糖原合酶活性的刺激作用:磷酸肌醇3激酶和p70核糖体蛋白-S6激酶参与其中的证据
Biochem J. 1995 Jan 1;305 ( Pt 1)(Pt 1):25-8. doi: 10.1042/bj3050025.
6
Normal activation of p70 S6 kinase by insulin in cells overexpressing dominant negative 85kD subunit of phosphoinositide 3-kinase.
Biochem Biophys Res Commun. 1995 Mar 17;208(2):735-41. doi: 10.1006/bbrc.1995.1399.
7
Cyclin D1 expression mediated by phosphatidylinositol 3-kinase through mTOR-p70(S6K)-independent signaling in growth factor-stimulated NIH 3T3 fibroblasts.在生长因子刺激的NIH 3T3成纤维细胞中,磷脂酰肌醇3激酶通过不依赖mTOR-p70(S6K)的信号传导介导细胞周期蛋白D1的表达。
Mol Cell Biol. 1999 Feb;19(2):1346-58. doi: 10.1128/MCB.19.2.1346.
8
The mitogenic and myogenic actions of insulin-like growth factors utilize distinct signaling pathways.胰岛素样生长因子的促有丝分裂和生肌作用利用不同的信号通路。
J Biol Chem. 1997 Mar 7;272(10):6653-62. doi: 10.1074/jbc.272.10.6653.
9
Temporal activation of p70 S6 kinase and Akt1 by insulin: PI 3-kinase-dependent and -independent mechanisms.胰岛素对p70 S6激酶和Akt1的瞬时激活:PI 3激酶依赖性和非依赖性机制。
Am J Physiol. 1998 Oct;275(4):E618-25. doi: 10.1152/ajpendo.1998.275.4.E618.
10
ATP-dependent choline phosphate-induced mitogenesis in fibroblasts involves activation of pp70 S6 kinase and phosphatidylinositol 3'-kinase through an extracellular site. Synergistic mitogenic effects of choline phosphate and sphingosine 1-phosphate.ATP 依赖性胆碱磷酸诱导成纤维细胞的有丝分裂发生涉及通过细胞外位点激活 pp70 S6 激酶和磷脂酰肌醇 3'-激酶。胆碱磷酸和鞘氨醇 1-磷酸的协同有丝分裂作用。
J Biol Chem. 1997 Jan 31;272(5):3064-72. doi: 10.1074/jbc.272.5.3064.

引用本文的文献

1
The therapeutic potential of insulin-like growth factor-1 in central nervous system disorders.胰岛素样生长因子-1在中枢神经系统疾病中的治疗潜力。
Neurosci Biobehav Rev. 2016 Apr;63:207-22. doi: 10.1016/j.neubiorev.2016.01.001. Epub 2016 Jan 15.
2
Control of cell cycle exit and entry by protein kinase B-regulated forkhead transcription factors.蛋白激酶B调控的叉头转录因子对细胞周期退出和进入的控制。
Mol Cell Biol. 2002 Apr;22(7):2025-36. doi: 10.1128/MCB.22.7.2025-2036.2002.
3
PI3-kinase p85alpha is a target molecule of proline-rich antimicrobial peptide to suppress proliferation of ras-transformed cells.PI3激酶p85α是富含脯氨酸的抗菌肽抑制ras转化细胞增殖的靶分子。
Jpn J Cancer Res. 2001 Sep;92(9):959-67. doi: 10.1111/j.1349-7006.2001.tb01187.x.
4
Activation of phosphatidylinositol-3 kinase (PI-3K) and extracellular regulated kinases (Erk1/2) is involved in muscarinic receptor-mediated DNA synthesis in neural progenitor cells.磷脂酰肌醇-3激酶(PI-3K)和细胞外调节激酶(Erk1/2)的激活参与了毒蕈碱受体介导的神经祖细胞中的DNA合成。
J Neurosci. 2001 Mar 1;21(5):1569-79. doi: 10.1523/JNEUROSCI.21-05-01569.2001.
5
Intracellular signals that control cell proliferation in mammalian balance epithelia: key roles for phosphatidylinositol-3 kinase, mammalian target of rapamycin, and S6 kinases in preference to calcium, protein kinase C, and mitogen-activated protein kinase.控制哺乳动物平衡上皮细胞增殖的细胞内信号:磷脂酰肌醇-3激酶、雷帕霉素哺乳动物靶蛋白和S6激酶相较于钙、蛋白激酶C和丝裂原活化蛋白激酶的关键作用。
J Neurosci. 2001 Jan 15;21(2):570-80. doi: 10.1523/JNEUROSCI.21-02-00570.2001.
6
Among translational effectors, p70S6k is uniquely sensitive to inhibition by glucocorticoids.在翻译效应因子中,p70S6k对糖皮质激素的抑制作用具有独特的敏感性。
Biochem J. 2000 Apr 15;347(Pt 2):389-97. doi: 10.1042/0264-6021:3470389.
7
Protein kinase A-dependent and -independent signaling pathways contribute to cyclic AMP-stimulated proliferation.蛋白激酶A依赖性和非依赖性信号通路有助于环磷酸腺苷刺激的增殖。
Mol Cell Biol. 1999 Sep;19(9):5882-91. doi: 10.1128/MCB.19.9.5882.
8
Cyclin D1 expression mediated by phosphatidylinositol 3-kinase through mTOR-p70(S6K)-independent signaling in growth factor-stimulated NIH 3T3 fibroblasts.在生长因子刺激的NIH 3T3成纤维细胞中,磷脂酰肌醇3激酶通过不依赖mTOR-p70(S6K)的信号传导介导细胞周期蛋白D1的表达。
Mol Cell Biol. 1999 Feb;19(2):1346-58. doi: 10.1128/MCB.19.2.1346.
9
Distinct roles for the p110alpha and hVPS34 phosphatidylinositol 3'-kinases in vesicular trafficking, regulation of the actin cytoskeleton, and mitogenesis.p110α和hVPS34磷脂酰肌醇3'-激酶在囊泡运输、肌动蛋白细胞骨架调节和有丝分裂发生中的不同作用。
J Cell Biol. 1998 Dec 14;143(6):1647-59. doi: 10.1083/jcb.143.6.1647.
10
A function for phosphatidylinositol 3-kinase beta (p85alpha-p110beta) in fibroblasts during mitogenesis: requirement for insulin- and lysophosphatidic acid-mediated signal transduction.磷脂酰肌醇3-激酶β(p85α-p110β)在成纤维细胞有丝分裂过程中的作用:胰岛素和溶血磷脂酸介导的信号转导的需求
Mol Cell Biol. 1998 Dec;18(12):7119-29. doi: 10.1128/MCB.18.12.7119.

本文引用的文献

1
Membrane localization of phosphatidylinositol 3-kinase is sufficient to activate multiple signal-transducing kinase pathways.磷脂酰肌醇3激酶的膜定位足以激活多种信号转导激酶途径。
Mol Cell Biol. 1996 Aug;16(8):4117-27. doi: 10.1128/MCB.16.8.4117.
2
Activation of phosphoinositide 3-kinase by interaction with Ras and by point mutation.通过与Ras相互作用及点突变激活磷酸肌醇3激酶。
EMBO J. 1996 May 15;15(10):2442-51.
3
Mouse p170 is a novel phosphatidylinositol 3-kinase containing a C2 domain.小鼠p170是一种含有C2结构域的新型磷脂酰肌醇3激酶。
J Biol Chem. 1996 Jun 7;271(23):13304-7. doi: 10.1074/jbc.271.23.13304.
4
Cpk is a novel class of Drosophila PtdIns 3-kinase containing a C2 domain.Cpk是一类新型的含有C2结构域的果蝇磷脂酰肌醇3激酶。
J Biol Chem. 1996 Jun 7;271(23):13892-9. doi: 10.1074/jbc.271.23.13892.
5
Wortmannin-sensitive trafficking pathways in Chinese hamster ovary cells. Differential effects on endocytosis and lysosomal sorting.中国仓鼠卵巢细胞中对渥曼青霉素敏感的运输途径。对内吞作用和溶酶体分选的不同影响。
J Biol Chem. 1996 May 3;271(18):10953-62. doi: 10.1074/jbc.271.18.10953.
6
EGF or PDGF receptors activate atypical PKClambda through phosphatidylinositol 3-kinase.表皮生长因子(EGF)或血小板衍生生长因子(PDGF)受体通过磷脂酰肌醇3激酶激活非典型蛋白激酶Cλ。
EMBO J. 1996 Feb 15;15(4):788-98.
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Structural and functional analysis of pp70S6k.pp70S6k的结构与功能分析
Proc Natl Acad Sci U S A. 1995 Dec 5;92(25):11696-700. doi: 10.1073/pnas.92.25.11696.
8
p70s6k function is essential for G1 progression.p70s6k功能对于G1期进程至关重要。
Nature. 1993 May 13;363(6425):170-2. doi: 10.1038/363170a0.
9
Phosphatidylinositol 3-kinase functions upstream of Ras and Raf in mediating insulin stimulation of c-fos transcription.磷脂酰肌醇3激酶在介导胰岛素对c-fos转录的刺激作用中,在Ras和Raf的上游发挥作用。
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10
Target of rapamycin in yeast, TOR2, is an essential phosphatidylinositol kinase homolog required for G1 progression.酵母中的雷帕霉素靶蛋白TOR2是G1期进程所必需的一种重要磷脂酰肌醇激酶同源物。
Cell. 1993 May 7;73(3):585-96. doi: 10.1016/0092-8674(93)90144-f.

p85-p110磷脂酰肌醇3'-激酶的特异性激活通过ras和p70 S6激酶依赖性途径刺激DNA合成。

Specific activation of p85-p110 phosphatidylinositol 3'-kinase stimulates DNA synthesis by ras- and p70 S6 kinase-dependent pathways.

作者信息

McIlroy J, Chen D, Wjasow C, Michaeli T, Backer J M

机构信息

Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

Mol Cell Biol. 1997 Jan;17(1):248-55. doi: 10.1128/MCB.17.1.248.

DOI:10.1128/MCB.17.1.248
PMID:8972205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC231749/
Abstract

We have developed a polyclonal antibody that activates the heterodimeric p85-p110 phosphatidylinositol (PI) 3'-kinase in vitro and in microinjected cells. Affinity purification revealed that the activating antibody recognized the N-terminal SH2 (NSH2) domain of p85, and the antibody increased the catalytic activity of recombinant p85-p110 dimers threefold in vitro. To study the role of endogenous PI 3'-kinase in intact cells, the activating anti-NSH2 antibody was microinjected into GRC + LR73 cells, a CHO cell derivative selected for tight quiescence during serum withdrawal. Microinjection of anti-NSH2 antibodies increased bromodeoxyuridine (BrdU) incorporation fivefold in quiescent cells and enhanced the response to serum. These data reflect a specific activation of PI 3'-kinase, as the effect was blocked by coinjection of the appropriate antigen (glutathione S-transferase-NSH2 domains from p85 alpha), coinjection of inhibitory anti-p110 antibodies, or treatment of cells with wortmannin. We used the activating antibodies to study signals downstream from PI 3'-kinase. Although treatment of cells with 50 nM rapamycin only partially decreased anti-NSH2-stimulated BrdU incorporation, coinjection with an anti-p70 S6 kinase antibody effectively blocked anti-NSH2-stimulated DNA synthesis. We also found that coinjection of inhibitory anti-ras antibodies blocked both serum- and anti-NSH2-stimulated BrdU incorporation by approximately 60%, and treatment of cells with a specific inhibitor of MEK abolished antibody-stimulated BrdU incorporation. We conclude that selective activation of physiological levels of PI 3'-kinase is sufficient to stimulate DNA synthesis in quiescent cells. PI 3'-kinase-mediated DNA synthesis requires both p70 S6 kinase and the P21ras/MEK pathway.

摘要

我们已研发出一种多克隆抗体,该抗体在体外及显微注射入细胞后能激活异源二聚体p85-p110磷脂酰肌醇(PI)3'-激酶。亲和纯化显示,激活抗体识别p85的N端SH2(NSH2)结构域,且该抗体在体外使重组p85-p110二聚体的催化活性提高了三倍。为研究内源性PI 3'-激酶在完整细胞中的作用,将激活抗NSH2抗体显微注射入GRC + LR73细胞,这是一种在血清撤除期间选择用于严格静止的CHO细胞衍生物。抗NSH2抗体的显微注射使静止细胞中的溴脱氧尿苷(BrdU)掺入增加了五倍,并增强了对血清的反应。这些数据反映了PI 3'-激酶的特异性激活,因为通过共注射适当的抗原(来自p85α的谷胱甘肽S-转移酶-NSH2结构域)、共注射抑制性抗p110抗体或用渥曼青霉素处理细胞,该效应被阻断。我们使用激活抗体来研究PI 3'-激酶下游的信号。尽管用50 nM雷帕霉素处理细胞仅部分降低了抗NSH2刺激的BrdU掺入,但与抗p70 S6激酶抗体共注射有效地阻断了抗NSH2刺激的DNA合成。我们还发现,共注射抑制性抗ras抗体可使血清和抗NSH2刺激的BrdU掺入均减少约60%,并且用MEK的特异性抑制剂处理细胞可消除抗体刺激的BrdU掺入。我们得出结论,PI 3'-激酶生理水平的选择性激活足以刺激静止细胞中的DNA合成。PI 3'-激酶介导的DNA合成需要p70 S6激酶和P21ras/MEK途径。