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1
Microinjection of follicle-enclosed mouse oocytes.对卵泡包裹的小鼠卵母细胞进行显微注射。
Methods Mol Biol. 2009;518:157-73. doi: 10.1007/978-1-59745-202-1_12.
2
Oocyte-specific expression of Gpr3 is required for the maintenance of meiotic arrest in mouse oocytes.Gpr3在卵母细胞中的特异性表达是维持小鼠卵母细胞减数分裂阻滞所必需的。
Dev Biol. 2005 Dec 15;288(2):397-404. doi: 10.1016/j.ydbio.2005.09.030. Epub 2005 Nov 11.
3
[Nonhormonal stimulation in vitro of oocyte maturation in sturgeons].[鲟鱼卵母细胞体外非激素刺激成熟]
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4
Synthesis of zona pellucida proteins by denuded and follicle-enclosed mouse oocytes during culture in vitro.体外培养期间,裸卵和卵泡包裹的小鼠卵母细胞对透明带蛋白的合成。
Proc Natl Acad Sci U S A. 1980 Feb;77(2):1029-33. doi: 10.1073/pnas.77.2.1029.
5
Disruption of gap junctional communication within the ovarian follicle induces oocyte maturation.卵巢卵泡内间隙连接通讯的破坏会诱导卵母细胞成熟。
Endocrinology. 2006 May;147(5):2280-6. doi: 10.1210/en.2005-1011. Epub 2006 Jan 26.
6
Quantification of oocyte-specific transcripts in follicle-enclosed oocytes during antral development and maturation in vitro.体外窦状卵泡发育和成熟过程中卵泡包绕卵母细胞内卵母细胞特异性转录本的定量分析。
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7
Biochemical studies of mammalian oogenesis: metabolic cooperativity between granulosa cells and growing mouse oocytes.哺乳动物卵母细胞发生的生化研究:颗粒细胞与生长中的小鼠卵母细胞之间的代谢协作。
Dev Biol. 1981 Jun;84(2):455-64. doi: 10.1016/0012-1606(81)90415-2.
8
A comparison of protein synthetic activity in in vitro cultured denuded and follicle-enclosed oocytes.体外培养的裸卵和卵泡包裹卵母细胞中蛋白质合成活性的比较。
Cell Biol Int Rep. 1983 Dec;7(12):1049-55. doi: 10.1016/0309-1651(83)90010-3.
9
Control of Mammalian Oocyte Development by Interactions with the Maternal Follicular Environment.通过与母体卵泡环境的相互作用对哺乳动物卵母细胞发育的调控
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Estrogen can signal through multiple pathways to regulate oocyte cyst breakdown and primordial follicle assembly in the neonatal mouse ovary.雌激素可通过多种途径发出信号,以调节新生小鼠卵巢中的卵母细胞囊肿破裂和原始卵泡组装。
J Endocrinol. 2009 Sep;202(3):407-17. doi: 10.1677/JOE-09-0109. Epub 2009 Jun 8.

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High-Survival Rate After Microinjection of Mouse Oocytes and Early Embryos With mRNA by Combining a Tip Pipette and Piezoelectric-Assisted Micromanipulator.通过结合尖端移液管和压电辅助显微操作器对小鼠卵母细胞和早期胚胎进行mRNA显微注射后的高存活率
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2
The BCL-2 pathway preserves mammalian genome integrity by eliminating recombination-defective oocytes.BCL-2 通路通过消除重组缺陷的卵母细胞来维持哺乳动物基因组的完整性。
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Untapped Reserves: Controlling Primordial Follicle Growth Activation.未开发的储备:控制原始卵泡生长激活。
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Macrophage colony-stimulating factor (M-CSF) is an intermediate in the process of luteinizing hormone-induced decrease in natriuretic peptide receptor 2 (NPR2) and resumption of oocyte meiosis.巨噬细胞集落刺激因子(M-CSF)是黄体生成素诱导的利钠肽受体 2(NPR2)减少和卵母细胞减数分裂恢复过程中的一个中间产物。
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8
Live imaging RNAi screen reveals genes essential for meiosis in mammalian oocytes.实时成像RNA干扰筛选揭示哺乳动物卵母细胞减数分裂所必需的基因。
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9
Embryonic Poly(A)-Binding Protein Is Required During Early Stages of Mouse Oocyte Development for Chromatin Organization, Transcriptional Silencing, and Meiotic Competence.胚胎多聚腺苷酸结合蛋白在小鼠卵母细胞发育早期对于染色质组织、转录沉默和减数分裂能力是必需的。
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Spire-type actin nucleators cooperate with Formin-2 to drive asymmetric oocyte division.螺旋状肌动蛋白成核因子与 Formin-2 共同驱动卵母细胞的不对称分裂。
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本文引用的文献

1
Quantitative microinjection of mouse oocytes and eggs.小鼠卵母细胞和卵子的定量显微注射。
Methods Mol Biol. 2009;518:135-56. doi: 10.1007/978-1-59745-202-1_11.
2
A G(s)-linked receptor maintains meiotic arrest in mouse oocytes, but luteinizing hormone does not cause meiotic resumption by terminating receptor-G(s) signaling.一种与G(s)偶联的受体维持小鼠卵母细胞的减数分裂停滞,但促黄体生成素不会通过终止受体-G(s)信号传导来引发减数分裂恢复。
Dev Biol. 2007 Oct 15;310(2):240-9. doi: 10.1016/j.ydbio.2007.07.017. Epub 2007 Jul 24.
3
Self-organization of MTOCs replaces centrosome function during acentrosomal spindle assembly in live mouse oocytes.在活的小鼠卵母细胞中,中心体缺失时纺锤体组装过程中,微管组织中心的自我组织取代了中心体的功能。
Cell. 2007 Aug 10;130(3):484-98. doi: 10.1016/j.cell.2007.06.025.
4
Meiotic resumption in response to luteinizing hormone is independent of a Gi family G protein or calcium in the mouse oocyte.在小鼠卵母细胞中,对促黄体生成素作出反应的减数分裂恢复独立于Gi家族G蛋白或钙。
Dev Biol. 2006 Nov 15;299(2):345-55. doi: 10.1016/j.ydbio.2006.07.039. Epub 2006 Aug 5.
5
Monitoring of cAMP synthesis and degradation in living cells.活细胞中环磷酸腺苷(cAMP)合成与降解的监测。
Physiology (Bethesda). 2006 Apr;21:86-92. doi: 10.1152/physiol.00057.2005.
6
Stops and starts in mammalian oocytes: recent advances in understanding the regulation of meiotic arrest and oocyte maturation.哺乳动物卵母细胞的停滞与启动:理解减数分裂停滞和卵母细胞成熟调控的最新进展
Reproduction. 2005 Dec;130(6):791-9. doi: 10.1530/rep.1.00793.
7
Oocyte-specific expression of Gpr3 is required for the maintenance of meiotic arrest in mouse oocytes.Gpr3在卵母细胞中的特异性表达是维持小鼠卵母细胞减数分裂阻滞所必需的。
Dev Biol. 2005 Dec 15;288(2):397-404. doi: 10.1016/j.ydbio.2005.09.030. Epub 2005 Nov 11.
8
Regulation of meiotic prophase arrest in mouse oocytes by GPR3, a constitutive activator of the Gs G protein.Gs G蛋白的组成型激活剂GPR3对小鼠卵母细胞减数分裂前期阻滞的调控
J Cell Biol. 2005 Oct 24;171(2):255-65. doi: 10.1083/jcb.200506194.
9
The Gs-linked receptor GPR3 maintains meiotic arrest in mammalian oocytes.与Gs蛋白偶联的受体GPR3维持哺乳动物卵母细胞的减数分裂阻滞。
Science. 2004 Dec 10;306(5703):1947-50. doi: 10.1126/science.1103974.
10
Quantitative microinjection of oocytes, eggs, and embryos.卵母细胞、卵子和胚胎的定量显微注射。
Methods Cell Biol. 2004;74:219-42. doi: 10.1016/s0091-679x(04)74010-8.

对卵泡包裹的小鼠卵母细胞进行显微注射。

Microinjection of follicle-enclosed mouse oocytes.

作者信息

Jaffe Laurinda A, Norris Rachael P, Freudzon Marina, Ratzan William J, Mehlmann Lisa M

机构信息

Department of Cell Biology, University of Connecticut Health Center, Farmington, CT, USA.

出版信息

Methods Mol Biol. 2009;518:157-73. doi: 10.1007/978-1-59745-202-1_12.

DOI:10.1007/978-1-59745-202-1_12
PMID:19085139
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3133608/
Abstract

The mammalian oocyte develops within a complex of somatic cells known as a follicle, within which signals from the somatic cells regulate the oocyte, and signals from the oocyte regulate the somatic cells. Because isolation of the oocyte from the follicle disrupts these communication pathways, oocyte physiology is best studied within an intact follicle. Here we describe methods for quantitative microinjection of follicle-enclosed mouse oocytes, thus allowing the introduction of signaling molecules as well as optical probes into the oocyte within its physiological environment.

摘要

哺乳动物的卵母细胞在一种称为卵泡的体细胞复合体中发育,其中体细胞发出的信号调节卵母细胞,而卵母细胞发出的信号调节体细胞。由于将卵母细胞从卵泡中分离会破坏这些通信途径,因此最好在完整的卵泡内研究卵母细胞生理学。在这里,我们描述了对卵泡包裹的小鼠卵母细胞进行定量显微注射的方法,从而能够在其生理环境中将信号分子以及光学探针引入卵母细胞。