• 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

Differential proliferation of fibroblasts cultured from normal and fibrotic human lungs.

作者信息

Raghu G, Chen Y Y, Rusch V, Rabinovitch P S

机构信息

Department of Medicine, University of Washington School of Medicine, Seattle 98195.

出版信息

Am Rev Respir Dis. 1988 Sep;138(3):703-8. doi: 10.1164/ajrccm/138.3.703.

DOI:10.1164/ajrccm/138.3.703
PMID:3202423
Abstract

We studied the behavior of the cell cycle of cultured, early-passage human diploid pulmonary fibroblastlike cells (HDPFC) when grown in the presence of several growth factors. The rates of growth and growth fractions were studied in cultures from different origins. As much as 85 +/- 5% (SE) of HDPFC cultured from specimens with early fibrosis were cycling when the cells were grown in basal media supplemented with 10% serum or growth factors. In contrast, 55% +/- 8% (SE) of HDPFC from normal lung and only 31% +/- 5% (SE) of HDPFC cultured from specimens with dense fibrosis were cycling in those culture conditions. Results obtained by removal of any of the five growth factors from the defined medium indicated that the altered growth patterns were not related to any single growth factor tested. These studies are consistent with the hypothesis that HDPFC cultured from specimens with early fibrosis have a greater proliferative potential than HDPFC from late fibrosis.

摘要

相似文献

1
Differential proliferation of fibroblasts cultured from normal and fibrotic human lungs.
Am Rev Respir Dis. 1988 Sep;138(3):703-8. doi: 10.1164/ajrccm/138.3.703.
2
Differential expression of the urokinase receptor in fibroblasts from normal and fibrotic human lungs.人正常肺组织和纤维化肺组织成纤维细胞中尿激酶受体的差异表达
Am J Respir Cell Mol Biol. 1996 Jul;15(1):78-87. doi: 10.1165/ajrcmb.15.1.8679225.
3
Heterogeneous proliferative characteristics of human adult lung fibroblast lines and clonally derived fibroblasts from control and fibrotic tissue.
Am Rev Respir Dis. 1988 Mar;137(3):579-84. doi: 10.1164/ajrccm/137.3.579.
4
Differential proliferation of rat lung fibroblasts induced by the platelet-derived growth factor-AA, -AB, and -BB isoforms secreted by rat alveolar macrophages.大鼠肺泡巨噬细胞分泌的血小板衍生生长因子-AA、-AB和-BB亚型诱导大鼠肺成纤维细胞的增殖差异
Am J Respir Cell Mol Biol. 1991 Dec;5(6):539-47. doi: 10.1165/ajrcmb/5.6.539.
5
[Proliferative characteristics of fibroblast lines derived from open lung biopsy specimens of patients with the usual interstitial pneumonia form of idiopathic pulmonary fibrosis].[来源于特发性肺纤维化普通间质性肺炎型患者开胸肺活检标本的成纤维细胞系的增殖特性]
Nihon Kyobu Shikkan Gakkai Zasshi. 1991 Sep;29(9):1143-9.
6
Phenotypic variability among density-fractionated human lung fibroblasts.密度分级分离的人肺成纤维细胞之间的表型变异性。
Am Rev Respir Dis. 1987 Jan;135(1):57-61. doi: 10.1164/arrd.1987.135.1.57.
7
Tectorigenin inhibits the in vitro proliferation and enhances miR-338* expression of pulmonary fibroblasts in rats with idiopathic pulmonary fibrosis.替告瑞宁抑制特发性肺纤维化大鼠肺成纤维细胞的体外增殖并增强 miR-338* 的表达。
J Ethnopharmacol. 2010 Aug 19;131(1):165-73. doi: 10.1016/j.jep.2010.06.022. Epub 2010 Jun 19.
8
L-iduronate-rich glycosaminoglycans inhibit growth of normal fibroblasts independently of serum or added growth factors.富含艾杜糖醛酸的糖胺聚糖可独立于血清或添加的生长因子抑制正常成纤维细胞的生长。
Exp Cell Res. 1993 May;206(1):93-9. doi: 10.1006/excr.1993.1124.
9
In vitro proliferation and lifespan of human diploid fibroblasts in serum-free BSA-containing medium.人二倍体成纤维细胞在含牛血清白蛋白的无血清培养基中的体外增殖及寿命
J Cell Physiol. 1982 May;111(2):155-62. doi: 10.1002/jcp.1041110206.
10
TGF-beta 1 stimulates cultured human fibroblasts to proliferate and produce tissue-like fibroplasia: a fibronectin matrix-dependent event.转化生长因子β1刺激培养的人成纤维细胞增殖并产生组织样纤维增生:这是一个依赖纤连蛋白基质的事件。
J Cell Physiol. 1997 Jan;170(1):69-80. doi: 10.1002/(SICI)1097-4652(199701)170:1<69::AID-JCP8>3.0.CO;2-J.

引用本文的文献

1
Repurposing flavopiridol as an inhaled therapeutic for pulmonary fibrosis.重新利用黄酮哌啶醇作为治疗肺纤维化的吸入性疗法。
Eur J Pharmacol. 2025 Oct 15;1005:178058. doi: 10.1016/j.ejphar.2025.178058. Epub 2025 Aug 13.
2
Clonal Expansion of Alveolar Fibroblast Progeny Drives Pulmonary Fibrosis.肺泡成纤维细胞后代的克隆性扩增驱动肺纤维化。
bioRxiv. 2025 Jun 3:2025.05.31.657194. doi: 10.1101/2025.05.31.657194.
3
The Plastic Interplay between Lung Regeneration Phenomena and Fibrotic Evolution: Current Challenges and Novel Therapeutic Perspectives.
肺再生现象与纤维化演变之间的塑料相互作用:当前的挑战和新的治疗观点。
Int J Mol Sci. 2023 Dec 31;25(1):547. doi: 10.3390/ijms25010547.
4
Idiopathic pulmonary fibrosis (IPF): disease pathophysiology, targets, and potential therapeutic interventions.特发性肺纤维化(IPF):疾病病理生理学、靶点和潜在的治疗干预措施。
Mol Cell Biochem. 2024 Sep;479(9):2181-2194. doi: 10.1007/s11010-023-04845-6. Epub 2023 Sep 14.
5
Inositol possesses antifibrotic activity and mitigates pulmonary fibrosis.肌醇具有抗纤维化活性,可减轻肺纤维化。
Respir Res. 2023 May 16;24(1):132. doi: 10.1186/s12931-023-02421-6.
6
Idiopathic Pulmonary Comorbidities and Mechanisms.特发性肺部合并症及其机制
Int J Inflam. 2021 Oct 13;2021:3963659. doi: 10.1155/2021/3963659. eCollection 2021.
7
Splicing factor SRSF6 mediates pleural fibrosis.剪接因子 SRSF6 介导胸膜纤维化。
JCI Insight. 2021 May 24;6(10):146197. doi: 10.1172/jci.insight.146197.
8
Targeting the AXL Receptor in Combating Smoking-related Pulmonary Fibrosis.靶向 AXL 受体防治与吸烟相关的肺纤维化。
Am J Respir Cell Mol Biol. 2021 Jun;64(6):734-746. doi: 10.1165/rcmb.2020-0303OC.
9
A Role for HAPLN1 During Phenotypic Modulation of Human Lung Fibroblasts In Vitro.HAPLN1 在体外人肺成纤维细胞表型调节中的作用。
J Histochem Cytochem. 2020 Nov;68(11):797-811. doi: 10.1369/0022155420966663. Epub 2020 Oct 16.
10
Upregulation of Potassium Voltage-Gated Channel Subfamily J Member 2 Levels in the Lungs of Patients with Idiopathic Pulmonary Fibrosis.特发性肺纤维化患者肺部钾电压门控通道亚家族 J 成员 2 水平上调。
Can Respir J. 2020 Feb 25;2020:3406530. doi: 10.1155/2020/3406530. eCollection 2020.