• 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

血清饥饿对增殖的3T3细胞大小增长与细胞分裂解离的即时影响。

Immediate effects of serum depletion on dissociation between growth in size and cell division in proliferating 3T3 cells.

作者信息

Larsson O, Dafgård E, Engström W, Zetterberg A

出版信息

J Cell Physiol. 1986 May;127(2):267-73. doi: 10.1002/jcp.1041270212.

DOI:10.1002/jcp.1041270212
PMID:3700482
Abstract

Proliferating nonconfluent 3T3 cells become committed to proceed through the cell cycle or to enter G0 during the first post-mitotic part of G1 (G1pm). The decision to proceed through G1pm is dependent on the presence of serum growth factors in the culture medium. Cells that have passed this particular growth-factor-dependent cell cycle stage are independent of serum growth factors and undergo mitosis on schedule. We report here that G1ps, S, and G2 cells cease to increase in size when serum is withdrawn. As a result the mitotic cell size after 8 hours serum starvation is reduced to approximately 60% of the normal mitotic cell. This reduced growth in cell size is due to a rapid decrease in protein synthesis and some increase in protein degradation. This dissociation between growth in size and cell-cycle progression within a single cell cycle provides a new approach to study the two processes separately.

摘要

增殖的未汇合3T3细胞在G1期的第一个有丝分裂后阶段(G1pm)决定继续进行细胞周期或进入G0期。决定是否继续进行G1pm取决于培养基中血清生长因子的存在。已经通过这个特定的依赖生长因子的细胞周期阶段的细胞不再依赖血清生长因子,并按计划进行有丝分裂。我们在此报告,当血清被去除时,G1ps、S期和G2期细胞的大小不再增加。因此,血清饥饿8小时后的有丝分裂细胞大小减少到正常有丝分裂细胞的约60%。细胞大小的这种减少是由于蛋白质合成的快速下降和蛋白质降解的一些增加。在单个细胞周期内,细胞大小的增长与细胞周期进程之间的这种分离为分别研究这两个过程提供了一种新方法。

相似文献

1
Immediate effects of serum depletion on dissociation between growth in size and cell division in proliferating 3T3 cells.血清饥饿对增殖的3T3细胞大小增长与细胞分裂解离的即时影响。
J Cell Physiol. 1986 May;127(2):267-73. doi: 10.1002/jcp.1041270212.
2
Kinetic analysis of regulatory events in G1 leading to proliferation or quiescence of Swiss 3T3 cells.对瑞士3T3细胞中导致增殖或静止的G1期调控事件的动力学分析。
Proc Natl Acad Sci U S A. 1985 Aug;82(16):5365-9. doi: 10.1073/pnas.82.16.5365.
3
The role of increased proteolysis in the atrophy and arrest of proliferation in serum-deprived fibroblasts.蛋白水解增加在血清剥夺的成纤维细胞萎缩和增殖停滞中的作用。
J Cell Physiol. 1984 Oct;121(1):189-98. doi: 10.1002/jcp.1041210124.
4
PTHrP and cell division: expression and localization of PTHrP in a keratinocyte cell line (HaCaT) during the cell cycle.甲状旁腺激素相关蛋白与细胞分裂:细胞周期中甲状旁腺激素相关蛋白在角质形成细胞系(HaCaT)中的表达与定位。
J Cell Physiol. 1997 Dec;173(3):433-46. doi: 10.1002/(SICI)1097-4652(199712)173:3<433::AID-JCP16>3.0.CO;2-C.
5
v-mos-transformed cells fail to enter quiescence but growth arrest in G1 following serum withdrawal.v-mos 转化细胞在血清撤出后无法进入静止期,但在 G1 期发生生长停滞。
Exp Cell Res. 1994 Jul;213(1):210-7. doi: 10.1006/excr.1994.1192.
6
The RI alpha subunit of protein kinase A controls serum dependency and entry into cell cycle of human mammary epithelial cells.
Oncogene. 1994 Nov;9(11):3233-40.
7
The relative effects of different types of growth factors on DNA replication, mitosis, and cellular enlargement.不同类型生长因子对DNA复制、有丝分裂和细胞增大的相对影响。
Cytometry. 1984 Jul;5(4):368-75. doi: 10.1002/cyto.990050413.
8
Kinetics of G1 progression in 3T6 and SV-3T3 cells following treatment by 25-hydroxycholesterol.
Cancer Res. 1986 Mar;46(3):1233-8.
9
Effect of stypoldione on cell cycle progression, DNA and protein synthesis, and cell division in cultured sea urchin embryos.斯替波定对培养的海胆胚胎细胞周期进程、DNA和蛋白质合成以及细胞分裂的影响。
Mol Pharmacol. 1983 Nov;24(3):500-8.
10
PPARgamma1 synthesis and adipogenesis in C3H10T1/2 cells depends on S-phase progression, but does not require mitotic clonal expansion.C3H10T1/2细胞中PPARγ1的合成及脂肪生成依赖于S期进程,但并不需要有丝分裂克隆扩增。
J Cell Biochem. 2004 Feb 1;91(2):336-53. doi: 10.1002/jcb.10743.

引用本文的文献

1
The potential for chemical mixtures from the environment to enable the cancer hallmark of sustained proliferative signalling.环境中的化学混合物促成持续增殖信号传导这一癌症标志的可能性。
Carcinogenesis. 2015 Jun;36 Suppl 1(Suppl 1):S38-60. doi: 10.1093/carcin/bgv030.
2
Loss of protooncogene c-Myc function impedes G1 phase progression both before and after the restriction point.原癌基因c-Myc功能的丧失会在限制点前后阻碍G1期进程。
Mol Biol Cell. 2003 Mar;14(3):823-35. doi: 10.1091/mbc.e02-10-0649.
3
Serum deprivation enhances DNA synthesis of human hepatoma SMMC7721 cells.
World J Gastroenterol. 1998 Apr;4(2):121-124. doi: 10.3748/wjg.v4.i2.121.
4
Metabolic iteration, evolution and cognition in cellular proliferation.细胞增殖中的代谢迭代、进化与认知
Experientia. 1987 Oct 15;43(10):1094-9. doi: 10.1007/BF01956046.