• 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

小鼠精原干细胞培养。

Culture of mouse spermatogonial stem cells.

作者信息

Nagano M, Avarbock M R, Leonida E B, Brinster C J, Brinster R L

机构信息

School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6009, USA.

出版信息

Tissue Cell. 1998 Aug;30(4):389-97. doi: 10.1016/s0040-8166(98)80053-0.

DOI:10.1016/s0040-8166(98)80053-0
PMID:9787472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5507671/
Abstract

Spermatogenesis occurs within the seminiferous tubules of mammals by a complex process that is highly organized, extremely efficient and very productive. At the foundation of this process is the spermatogonial stem cell that is capable of both self-renewal and production of progeny cells, which undergo differentiation over a period of weeks to months in order to generate mature spermatozoa. It had been thought that germ cells survive only a brief period in culture, generally less than a few weeks. However, an accurate assessment of the presence of spermatogonial stem cells in any cell population has only recently become possible with development of the spermatogonial transplantation technique. Using this technique, we have demonstrated that mouse spermatogonial stem cells can be maintained in culture for approximately 4 months and will generate spermatogenesis following transplantation to the seminiferous tubules of an appropriate recipient. Extensive areas of cultured donor cell-derived spermatogenesis are generated in the host, and production of mature spermatozoa occurs. Cultivation of the testis cells on STO feeders is beneficial to stem cell survival. These results provide the first step in establishing a system that will permit spermatogonial stem cells to be cultivated and their number increased in vitro to allow for genetic modification before transplantation to a recipient testis.

摘要

精子发生过程在哺乳动物的生精小管内通过一个高度有序、极其高效且产量很高的复杂过程进行。这个过程的基础是精原干细胞,它既能自我更新,又能产生子代细胞,这些子代细胞会在数周乃至数月的时间里经历分化,以生成成熟的精子。过去人们认为生殖细胞在培养环境中只能存活很短一段时间,通常不到几周。然而,随着精原细胞移植技术的发展,最近才有可能准确评估任何细胞群体中精原干细胞的存在情况。利用这项技术,我们已经证明,小鼠精原干细胞可以在培养环境中维持约4个月,并且在移植到合适受体的生精小管后能够产生精子发生。宿主中会产生大量源自培养的供体细胞的精子发生区域,并且会产生成熟的精子。在STO饲养层上培养睾丸细胞有利于干细胞存活。这些结果为建立一个系统迈出了第一步,该系统将允许精原干细胞在体外进行培养并增加其数量,以便在移植到受体睾丸之前进行基因改造。

相似文献

1
Culture of mouse spermatogonial stem cells.小鼠精原干细胞培养。
Tissue Cell. 1998 Aug;30(4):389-97. doi: 10.1016/s0040-8166(98)80053-0.
2
Anchorage-independent growth of mouse male germline stem cells in vitro.体外培养的小鼠雄性生殖干细胞的锚定非依赖性生长。
Biol Reprod. 2006 Mar;74(3):522-9. doi: 10.1095/biolreprod.105.046441. Epub 2005 Nov 23.
3
Spermatogonial stem cell transplantation, cryopreservation and culture.精原干细胞移植、冷冻保存及培养
Semin Cell Dev Biol. 1998 Aug;9(4):401-9. doi: 10.1006/scdb.1998.0205.
4
Computer assisted image analysis to assess colonization of recipient seminiferous tubules by spermatogonial stem cells from transgenic donor mice.计算机辅助图像分析,用于评估来自转基因供体小鼠的精原干细胞对受体生精小管的定植情况。
Mol Reprod Dev. 1999 Jun;53(2):142-8. doi: 10.1002/(SICI)1098-2795(199906)53:2<142::AID-MRD3>3.0.CO;2-O.
5
Proliferation of mouse spermatogonial stem cells in microdrop culture.微滴培养中鼠精原干细胞的增殖。
Biol Reprod. 2010 Dec;83(6):951-7. doi: 10.1095/biolreprod.109.082800. Epub 2010 Aug 11.
6
Pattern and kinetics of mouse donor spermatogonial stem cell colonization in recipient testes.小鼠供体精原干细胞在受体睾丸中定植的模式和动力学
Biol Reprod. 1999 Jun;60(6):1429-36. doi: 10.1095/biolreprod60.6.1429.
7
Spermatogonial stem cells derived from infertile Wv/Wv mice self-renew in vitro and generate progeny following transplantation.源自不育Wv/Wv小鼠的精原干细胞在体外自我更新,并在移植后产生后代。
Biol Reprod. 2009 Aug;81(2):293-301. doi: 10.1095/biolreprod.109.075960. Epub 2009 Apr 15.
8
Transplantation of testis germinal cells into mouse seminiferous tubules.将睾丸生殖细胞移植到小鼠生精小管中。
Int J Dev Biol. 1997 Feb;41(1):111-22.
9
Characterization of spermatogonial stem cell maturation and differentiation in neonatal mice.新生小鼠精原干细胞成熟与分化的特征分析
Biol Reprod. 2003 Dec;69(6):2085-91. doi: 10.1095/biolreprod.103.017020. Epub 2003 Sep 3.
10
Germline transmission of donor haplotype following spermatogonial transplantation.精原细胞移植后供体单倍型的种系传递。
Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11303-7. doi: 10.1073/pnas.91.24.11303.

引用本文的文献

1
The use of deidentified organ donor testes for research.使用经过身份识别去除处理的器官捐献者睾丸进行研究。
Andrology. 2025 Feb 6. doi: 10.1111/andr.70008.
2
Spermatogonial stem cell technologies: applications from human medicine to wildlife conservation†.精原干细胞技术:从人类医学到野生动物保护的应用†。
Biol Reprod. 2024 Oct 14;111(4):757-779. doi: 10.1093/biolre/ioae109.
3
Induction of Meiotic Initiation in Long-Term Mouse Spermatogonial Stem Cells Under Retinoid Acid and Nutrient Restriction Conditions.在维 A 酸和营养限制条件下诱导长期小鼠精原干细胞的减数分裂起始。

本文引用的文献

1
Spermatogonial transplantation and reconstitution of donor cell spermatogenesis in recipient mice.精原细胞移植及受体小鼠中供体细胞精子发生的重建
APMIS. 1998 Jan;106(1):47-55; discussion 56-7. doi: 10.1111/j.1699-0463.1998.tb01318.x.
2
Disruption of overlapping transcripts in the ROSA beta geo 26 gene trap strain leads to widespread expression of beta-galactosidase in mouse embryos and hematopoietic cells.ROSA βgeo 26基因捕获品系中重叠转录本的破坏导致β-半乳糖苷酶在小鼠胚胎和造血细胞中广泛表达。
Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):3789-94. doi: 10.1073/pnas.94.8.3789.
3
Transplantation of testis germinal cells into mouse seminiferous tubules.
Methods Mol Biol. 2024;2770:113-121. doi: 10.1007/978-1-0716-3698-5_9.
4
Characterization of long-term expansion of tree shrew spermatogonial stem cells.树鼩精原干细胞长期扩增的特性研究。
Zool Res. 2023 Nov 18;44(6):1080-1094. doi: 10.24272/j.issn.2095-8137.2023.317.
5
Rattus norvegicus Spermatogenesis Colony-Forming Assays.挪威褐家鼠精子发生集落形成分析。
Methods Mol Biol. 2023;2677:233-257. doi: 10.1007/978-1-0716-3259-8_14.
6
Perspectives: Methods for Evaluating Primate Spermatogonial Stem Cells.观点:评估灵长类精原干细胞的方法。
Methods Mol Biol. 2023;2656:341-364. doi: 10.1007/978-1-0716-3139-3_18.
7
Primary Cultures of Spermatogonia and Testis Cells.精原细胞和睪丸细胞的原代培养。
Methods Mol Biol. 2023;2656:127-143. doi: 10.1007/978-1-0716-3139-3_7.
8
Efficacy of leaf extract on morphological and molecular behavior of mice germ stem cells.叶提取物对小鼠生殖干细胞形态和分子行为的功效。
Anim Reprod. 2022 Aug 19;19(2):e20220036. doi: 10.1590/1984-3143-AR2022-0036. eCollection 2022.
9
Analysis of chromatin accessibility in p53 deficient spermatogonial stem cells for high frequency transformation into pluripotent state.分析 p53 缺陷精原干细胞中的染色质可及性,以实现高频率转化为多能状态。
Cell Prolif. 2022 Mar;55(3):e13195. doi: 10.1111/cpr.13195. Epub 2022 Feb 4.
10
In Vitro Culturing of Adult Stem Cells: The Importance of Serum and Atmospheric Oxygen.成体干细胞的体外培养:血清和大气氧的重要性。
Adv Exp Med Biol. 2022;1376:101-118. doi: 10.1007/5584_2021_656.
将睾丸生殖细胞移植到小鼠生精小管中。
Int J Dev Biol. 1997 Feb;41(1):111-22.
4
Regulatory mechanisms in stem cell biology.干细胞生物学中的调控机制。
Cell. 1997 Feb 7;88(3):287-98. doi: 10.1016/s0092-8674(00)81867-x.
5
Ultrastructural observations of spermatogenesis in mice resulting from transplantation of mouse spermatogonia.小鼠精原细胞移植后小鼠精子发生的超微结构观察
J Androl. 1996 Nov-Dec;17(6):603-14.
6
Reconstitution of spermatogenesis from frozen spermatogonial stem cells.从冷冻的精原干细胞重建精子发生。
Nat Med. 1996 Jun;2(6):693-6. doi: 10.1038/nm0696-693.
7
Purification, culture, and fractionation of spermatogenic cells.生精细胞的纯化、培养和分级分离。
Methods Enzymol. 1993;225:84-113. doi: 10.1016/0076-6879(93)25009-q.
8
Immortalized germ cells undergo meiosis in vitro.永生化生殖细胞在体外进行减数分裂。
Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5533-7. doi: 10.1073/pnas.91.12.5533.
9
Mammalian spermatogenesis in vivo and in vitro: a partnership of spermatogenic and somatic cell lineages.哺乳动物体内和体外的精子发生:生精细胞谱系与体细胞谱系的协同作用
Endocr Rev. 1994 Feb;15(1):116-34. doi: 10.1210/edrv-15-1-116.
10
Germline transmission of donor haplotype following spermatogonial transplantation.精原细胞移植后供体单倍型的种系传递。
Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11303-7. doi: 10.1073/pnas.91.24.11303.