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1
Effect of medium composition on protein degradation and DNA synthesis in rat embryo fibroblasts.培养基成分对大鼠胚胎成纤维细胞中蛋白质降解和DNA合成的影响。
Proc Natl Acad Sci U S A. 1977 Jun;74(6):2427-31. doi: 10.1073/pnas.74.6.2427.
2
Heparin-binding growth factors stimulate DNA synthesis in rat alveolar type II cells.肝素结合生长因子刺激大鼠Ⅱ型肺泡细胞的DNA合成。
Am J Respir Cell Mol Biol. 1990 Jan;2(1):99-106. doi: 10.1165/ajrcmb/2.1.99.
3
Stimulation of division of sparse and confluent 3T3 cell populations by a fibroblast growth factor, dexamethasone, and insulin.成纤维细胞生长因子、地塞米松和胰岛素对稀疏及汇合状态的3T3细胞群体分裂的刺激作用。
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4584-8. doi: 10.1073/pnas.71.11.4584.
4
Effect of rous sarcoma virus transformation of rat-1 fibroblasts upon their growth factor and anchorage requirements in serum-free medium.劳氏肉瘤病毒对大鼠-1成纤维细胞的转化对其在无血清培养基中生长因子及贴壁需求的影响。
Cancer Res. 1983 May;43(5):2121-30.
5
Synthesis of multiplication-stimulating activity (rat insulin-like growth factor II) by rat embryo fibroblasts.大鼠胚胎成纤维细胞合成增殖刺激活性物质(大鼠胰岛素样生长因子II)。
Endocrinology. 1983 Mar;112(3):979-87. doi: 10.1210/endo-112-3-979.
6
Comparative effects of somatomedin C and insulin on the metabolism and growth of cultured human fibroblasts.生长介素C与胰岛素对培养的人成纤维细胞代谢和生长的比较作用
J Cell Physiol. 1985 Jan;122(1):133-41. doi: 10.1002/jcp.1041220120.
7
Keratinocyte growth factor and hepatocyte growth factor/scatter factor are heparin-binding growth factors for alveolar type II cells in fibroblast-conditioned medium.角质形成细胞生长因子和肝细胞生长因子/散射因子是成纤维细胞条件培养基中肺泡II型细胞的肝素结合生长因子。
J Clin Invest. 1993 Aug;92(2):969-77. doi: 10.1172/JCI116673.
8
Regulation of intracellular protein degradation in IMR-90 human diploid fibroblasts.
J Cell Physiol. 1983 May;115(2):167-74. doi: 10.1002/jcp.1041150210.
9
Human epidermal growth factor and the proliferation of human fibroblasts.人表皮生长因子与人成纤维细胞的增殖
J Cell Physiol. 1976 Jun;88(2):227-37. doi: 10.1002/jcp.1040880212.
10
Growth factor regulation of membrane transport in human fibroblasts and its relationship to stimulation of DNA synthesis.人成纤维细胞中膜转运的生长因子调节及其与DNA合成刺激的关系。
J Cell Physiol. 1985 Dec;125(3):443-8. doi: 10.1002/jcp.1041250312.

引用本文的文献

1
Enrichment and detection of molecules secreted by tumor cells using magnetic reversed-phase particles and LC-MALDI-TOF-MS.利用磁性反相颗粒和液相色谱-基质辅助激光解吸电离飞行时间质谱对肿瘤细胞分泌的分子进行富集和检测。
J Biomol Tech. 2007 Dec;18(5):287-97.
2
Control of cell protein catabolism in rat liver. Effects of starvation and administration of cycloheximide.大鼠肝脏细胞蛋白质分解代谢的调控。饥饿及给予环己酰亚胺的影响。
Biochem J. 1982 Aug 15;206(2):395-405. doi: 10.1042/bj2060395.
3
Fine structure of arterial smooth muscle cells cultured in the presence of whole blood serum or plasma-derived serum.在全血血清或血浆源性血清存在的情况下培养的动脉平滑肌细胞的精细结构。
Cell Tissue Res. 1982;223(1):87-99. doi: 10.1007/BF00221501.
4
Degradation of proteins microinjected into IMR-90 human diploid fibroblasts.微注射到IMR - 90人二倍体成纤维细胞中的蛋白质的降解
J Cell Biol. 1981 Oct;91(1):184-94. doi: 10.1083/jcb.91.1.184.
5
Regulation of the production of secretory proteins: intracellular degradation of newly synthesized "defective" collagen.分泌蛋白产生的调控:新合成的“缺陷”胶原蛋白的细胞内降解
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4746-50. doi: 10.1073/pnas.77.8.4746.
6
Protein turnover and proliferation. Turnover kinetics associated with the elevation of 3T3-cell acid-proteinase activity and cessation of net protein gain.蛋白质周转与增殖。与3T3细胞酸性蛋白酶活性升高及净蛋白质增加停止相关的周转动力学。
Biochem J. 1982 Aug 15;206(2):239-49. doi: 10.1042/bj2060239.
7
Regulation of catabolism of microinjected ribonuclease A requires the amino-terminal 20 amino acids.显微注射的核糖核酸酶A分解代谢的调控需要氨基末端的20个氨基酸。
Proc Natl Acad Sci U S A. 1983 Apr;80(8):2166-70. doi: 10.1073/pnas.80.8.2166.
8
Distinct proteolytic mechanisms in serum-sufficient and serum-restricted fibroblasts. Transformed 3T3 cells fail to regulate proteolysis in relation to culture density only during serum-sufficiency.血清充足和血清受限的成纤维细胞中不同的蛋白水解机制。仅在血清充足时,转化的3T3细胞在与培养密度相关的情况下无法调节蛋白水解。
Biochem J. 1984 Jul 1;221(1):53-60. doi: 10.1042/bj2210053.
9
Protein turnover and proliferation. Failure of SV-3T3 cells to increase lysosomal proteinases, increase protein degradation and cease net protein accumulation.蛋白质周转与增殖。SV - 3T3细胞未能增加溶酶体蛋白酶、增强蛋白质降解并停止净蛋白质积累。
Biochem J. 1982 Aug 15;206(2):251-8. doi: 10.1042/bj2060251.
10
Stimulation by glucocorticoids of protein degradation in hepatocyte monolayers.糖皮质激素对肝细胞单层中蛋白质降解的刺激作用。
Biochem J. 1981 Apr 15;196(1):33-40. doi: 10.1042/bj1960033.

本文引用的文献

1
The initiation of cell division in a contact-inhibited mammalian cell line.接触抑制的哺乳动物细胞系中细胞分裂的起始
J Cell Physiol. 1965 Dec;66(3):325-33. doi: 10.1002/jcp.1030660310.
2
Early alterations in amino acid pools and protein synthesis of diploid fibroblasts stimulated to synthesize DNA by addition of serum.通过添加血清刺激二倍体成纤维细胞合成DNA时,其氨基酸库和蛋白质合成的早期变化。
J Cell Physiol. 1969 Oct;74(2):191-202. doi: 10.1002/jcp.1040740211.
3
Stimulation of glucose transport in cultures of density-inhibited chick embryo cells.密度抑制的鸡胚细胞培养物中葡萄糖转运的刺激作用。
Proc Natl Acad Sci U S A. 1971 Dec;68(12):3154-7. doi: 10.1073/pnas.68.12.3154.
4
"Pleiotypic response".多型性反应
Nat New Biol. 1971 Aug;232(33):206-11.
5
"Contact inhibition" of cell division in 3T3 cells.3T3细胞中细胞分裂的“接触抑制”
Proc Natl Acad Sci U S A. 1968 May;60(1):300-4. doi: 10.1073/pnas.60.1.300.
6
Suppression of protein turnover by amino acids in the perfused rat liver.灌注大鼠肝脏中氨基酸对蛋白质周转的抑制作用。
J Biol Chem. 1972 Oct 25;247(20):6474-81.
7
Protein degradation in cultured cells. The effect of fresh medium, fluoride, and iodoacetate on the digestion of cellular protein of rat fibroblasts.培养细胞中的蛋白质降解。新鲜培养基、氟化物和碘乙酸对大鼠成纤维细胞细胞蛋白质消化的影响。
J Biol Chem. 1973 Sep 10;248(17):6221-6.
8
Control of the initiation of DNA synthesis in 3T3 cells: low-molecular weight nutrients.3T3细胞中DNA合成起始的调控:低分子量营养素
Proc Natl Acad Sci U S A. 1974 Aug;71(8):2942-5. doi: 10.1073/pnas.71.8.2942.
9
Control of the initiation of DNA synthesis in 3T3 cells: serum factors.3T3细胞中DNA合成起始的控制:血清因子
Proc Natl Acad Sci U S A. 1974 Jul;71(7):2908-11. doi: 10.1073/pnas.71.7.2908.
10
Regulation of RNA synthesis in fibroblasts during transition from resting to growing state.成纤维细胞从静止状态转变为生长状态过程中RNA合成的调控。
Proc Natl Acad Sci U S A. 1973 Oct;70(10):2819-22. doi: 10.1073/pnas.70.10.2819.

培养基成分对大鼠胚胎成纤维细胞中蛋白质降解和DNA合成的影响。

Effect of medium composition on protein degradation and DNA synthesis in rat embryo fibroblasts.

作者信息

Warburton M J, Poole B

出版信息

Proc Natl Acad Sci U S A. 1977 Jun;74(6):2427-31. doi: 10.1073/pnas.74.6.2427.

DOI:10.1073/pnas.74.6.2427
PMID:267935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC432185/
Abstract

Fibroblasts in medium deficient in serum, amino acids, phosphate, or glucose stop synthesizing DNA and increase the rate of degradation of their long-lived cellular proteins approximately 2-fold. There is no difference in the rate of degradation of short-lived proteins under these conditions. Insulin, dexamethasone, and fibroblast growth factor act synergistically to inhibit protein degradation and to stimulate thymidine incorporation to about the same extent as serum. When the medium content in serum or fibroblast growth factor is varied over a wide range, there is a close, inverse correlation between the rate of protein degradation and the extent of thymidine incorporation. When serum is added to cells that have been deprived of serum, the inhibition of protein degradation is immediate whereas the enhanced rate of protein degradation in serum-free medium is attained within 1 hr after serum removal. A 30-min exposure to serum followed by incubation in serum-free medium was as effective as continuous exposure to serum in stimulating thymidine incorporation after 8-24 hr.

摘要

在缺乏血清、氨基酸、磷酸盐或葡萄糖的培养基中,成纤维细胞停止合成DNA,并将其长寿命细胞蛋白的降解速率提高约2倍。在这些条件下,短寿命蛋白的降解速率没有差异。胰岛素、地塞米松和成纤维细胞生长因子协同作用,抑制蛋白降解,并刺激胸苷掺入,其程度与血清大致相同。当血清或成纤维细胞生长因子的培养基含量在很宽的范围内变化时,蛋白降解速率与胸苷掺入程度之间存在密切的负相关。当向已剥夺血清的细胞中添加血清时,对蛋白降解的抑制是即时的,而在无血清培养基中蛋白降解速率的提高在去除血清后1小时内即可达到。在无血清培养基中孵育前,先暴露于血清30分钟,在8-24小时后刺激胸苷掺入的效果与持续暴露于血清相同。