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1
Mouse chimeras as a system to investigate development, cell and tissue function, disease mechanisms and organ regeneration.小鼠嵌合体作为一种研究发育、细胞和组织功能、疾病机制和器官再生的系统。
Cell Cycle. 2011 Jul 1;10(13):2091-9. doi: 10.4161/cc.10.13.16360.
2
Stem cell potency and the ability to contribute to chimeric organisms.干细胞的多能性及其对嵌合体生物的贡献能力。
Reproduction. 2013 Mar 7;145(3):R81-8. doi: 10.1530/REP-12-0396. Print 2013 Mar 1.
3
Developmental fate of single embryonic stem cells microinjected into 8-cell-stage mouse embryos.显微注射到8细胞期小鼠胚胎中的单个胚胎干细胞的发育命运。
Differentiation. 1997 Oct;62(1):1-11. doi: 10.1046/j.1432-0436.1997.6210001.x.
4
Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting.雄激素源性小鼠胚胎干细胞具有多能性,并在嵌合体中导致骨骼缺陷:对基因印记的影响。
Cell. 1990 Jul 27;62(2):251-60. doi: 10.1016/0092-8674(90)90363-j.
5
Generation of chimeras by aggregation of embryonic stem cells with diploid or tetraploid mouse embryos.通过将胚胎干细胞与二倍体或四倍体小鼠胚胎聚集来产生嵌合体。
Methods Mol Biol. 2011;693:37-56. doi: 10.1007/978-1-60761-974-1_3.
6
Building brains: neural chimeras in the study of nervous system development and repair.构建大脑:神经系统发育与修复研究中的神经嵌合体
Brain Pathol. 1999 Jul;9(3):527-45. doi: 10.1111/j.1750-3639.1999.tb00540.x.
7
[Formation of germline chimeras from murine embryonic stem cell lines].[从鼠胚胎干细胞系形成种系嵌合体]
Yi Chuan Xue Bao. 1999;26(2):126-34.
8
Development to term of mouse androgenetic aggregation chimeras.小鼠孤雄聚集嵌合体发育至足月。
Development. 1991 Dec;113(4):1325-33. doi: 10.1242/dev.113.4.1325.
9
Producing fully ES cell-derived mice from eight-cell stage embryo injections.通过八细胞期胚胎注射产生完全由胚胎干细胞衍生的小鼠。
Methods Enzymol. 2010;476:285-94. doi: 10.1016/S0076-6879(10)76016-X.
10
A novel retrovirally induced embryonic lethal mutation in the mouse: assessment of the developmental fate of embryonic stem cells homozygous for the 413.d proviral integration.小鼠中一种由逆转录病毒诱导的新型胚胎致死突变:对413.d原病毒整合纯合的胚胎干细胞发育命运的评估。
Development. 1991 Apr;111(4):969-81. doi: 10.1242/dev.111.4.969.

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Phenotypic Analysis of Early Neurogenesis in a Mouse Chimeric Embryo and Stem Cell-Based Neuruloid Model.鼠嵌合体胚胎和基于干细胞类神经胚模型中的早期神经发生的表型分析。
Methods Mol Biol. 2024;2746:165-177. doi: 10.1007/978-1-0716-3585-8_14.
2
Efficient simultaneous double DNA knock-in in murine embryonic stem cells by CRISPR/Cas9 ribonucleoprotein-mediated circular plasmid targeting for generating gene-manipulated mice.利用 CRISPR/Cas9 核糖核蛋白介导的环状质粒靶向进行高效的同时双重 DNA 敲入,用于生成基因修饰小鼠。
Sci Rep. 2022 Dec 13;12(1):21558. doi: 10.1038/s41598-022-26107-z.
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Interspecies Chimeric Barriers for Generating Exogenic Organs and Cells for Transplantation.用于移植的外源性器官和细胞的种间嵌合体屏障。
Cell Transplant. 2022 Jan-Dec;31:9636897221110525. doi: 10.1177/09636897221110525.
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Exploring the Genetic Conception of Obesity via the Dual Role of FoxO.通过 FoxO 的双重作用探索肥胖的遗传概念。
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Limitation of adipose tissue by the number of embryonic progenitor cells.胚胎祖细胞数量限制脂肪组织。
Elife. 2020 May 26;9:e53074. doi: 10.7554/eLife.53074.
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CORP: Using transgenic mice to study skeletal muscle physiology.公司:利用转基因小鼠研究骨骼肌生理学。
J Appl Physiol (1985). 2020 May 1;128(5):1227-1239. doi: 10.1152/japplphysiol.00021.2020. Epub 2020 Feb 27.
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Generation of bioartificial hearts using decellularized scaffolds and mixed cells.使用脱细胞支架和混合细胞生成生物人工心脏。
Biomed Eng Online. 2019 Jun 4;18(1):71. doi: 10.1186/s12938-019-0691-9.
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Cell fusion in the liver, revisited.肝脏中的细胞融合,再探讨。
World J Hepatol. 2018 Feb 27;10(2):213-221. doi: 10.4254/wjh.v10.i2.213.
9
Selection against BALB/c strain cells in mouse chimaeras.在小鼠嵌合体中对BALB/c品系细胞的选择淘汰。
Biol Open. 2018 Jan 12;7(1):bio030189. doi: 10.1242/bio.030189.
10
Mouse Parthenogenetic Embryonic Stem Cells with Biparental-Like Expression of Imprinted Genes Generate Cortical-Like Neurons That Integrate into the Injured Adult Cerebral Cortex.具有双亲样印迹基因表达的小鼠孤雌生殖胚胎干细胞产生皮质样神经元,并整合到损伤的成年大脑皮层中。
Stem Cells. 2018 Feb;36(2):192-205. doi: 10.1002/stem.2721. Epub 2017 Nov 10.

本文引用的文献

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Unrestricted lineage differentiation of parthenogenetic ES cells.孤雌生殖胚胎干细胞的无限制谱系分化。
Dev Genes Evol. 1997 Jan;206(6):377-388. doi: 10.1007/s004270050067.
2
Generation of rat pancreas in mouse by interspecific blastocyst injection of pluripotent stem cells.利用种间囊胚注射多能干细胞在鼠体内生成大鼠胰腺。
Cell. 2010 Sep 3;142(5):787-99. doi: 10.1016/j.cell.2010.07.039.
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Viable rat-mouse chimeras: where do we go from here?可行的大鼠-小鼠嵌合体:我们的下一步在哪里?
Cell. 2010 Sep 3;142(5):676-8. doi: 10.1016/j.cell.2010.08.021.
4
Chimerism resulting from parthenogenetic activation and dispermic fertilization.孤雌激活和双精受精导致的嵌合体。
Am J Med Genet A. 2010 Sep;152A(9):2277-86. doi: 10.1002/ajmg.a.33594.
5
Clonal and territorial development of the pancreas as revealed by eGFP-labelled mouse chimeras.通过 GFP 标记的小鼠嵌合体揭示胰腺的克隆和区域发育。
Cell Tissue Res. 2010 Oct;342(1):31-8. doi: 10.1007/s00441-010-1028-y. Epub 2010 Aug 29.
6
Induced pluripotent stem cell-derived hepatocytes have the functional and proliferative capabilities needed for liver regeneration in mice.诱导多能干细胞衍生的肝细胞具有在小鼠中进行肝脏再生所需的功能和增殖能力。
J Clin Invest. 2010 Sep;120(9):3120-6. doi: 10.1172/JCI43267. Epub 2010 Aug 25.
7
Chimeric mice with humanized liver: tools for the study of drug metabolism, excretion, and toxicity.具有人源化肝脏的嵌合小鼠:用于药物代谢、排泄和毒性研究的工具。
Methods Mol Biol. 2010;640:491-509. doi: 10.1007/978-1-60761-688-7_27.
8
Blood chimerism in a girl with Down syndrome and possible freemartin effect leading to aplasia of the Müllerian derivatives.唐氏综合征女孩的血液嵌合体和可能的雌雄同体效应导致 Müllerian 衍生物发育不良。
Hum Reprod. 2010 May;25(5):1339-43. doi: 10.1093/humrep/deq048. Epub 2010 Feb 26.
9
W41/W41 blastocyst complementation: a system for genetic modeling of hematopoiesis.W41/W41 囊胚互补:一种造血遗传建模系统。
Blood. 2010 Jan 7;115(1):47-50. doi: 10.1182/blood-2009-07-235622. Epub 2009 Oct 28.
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Renaissance for mouse models of human hematopoiesis and immunobiology.人类造血与免疫生物学小鼠模型的复兴。
Nat Immunol. 2009 Oct;10(10):1039-42. doi: 10.1038/ni1009-1039.

小鼠嵌合体作为一种研究发育、细胞和组织功能、疾病机制和器官再生的系统。

Mouse chimeras as a system to investigate development, cell and tissue function, disease mechanisms and organ regeneration.

机构信息

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

出版信息

Cell Cycle. 2011 Jul 1;10(13):2091-9. doi: 10.4161/cc.10.13.16360.

DOI:10.4161/cc.10.13.16360
PMID:21606677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3230469/
Abstract

Chimeras are organisms composed of at least two genetically distinct cell lineages originating from different zygotes. In the laboratory, mouse chimeras can be produced experimentally; various techniques allow combining different early stage mouse embryos with each other or with pluripotent stem cells. Identification of the progeny of the different lineages in chimeras permits to follow cell fate and function, enabling correlation of genotype with phenotype. Mouse chimeras have become a tool to investigate critical developmental processes, including cell specification, differentiation, patterning, and the function of specific genes. In addition, chimeras can also be generated to address biological processes in the adult, including mechanisms underlying diseases or tissue repair and regeneration. This review summarizes the different types of chimeras and how they have been generated and provides examples of how mouse chimeras offer a unique and powerful system to investigate questions pertaining to cell and tissue function in the developing and adult organism.

摘要

嵌合体是由至少两个来自不同受精卵的遗传上不同的细胞谱系组成的生物体。在实验室中,可以通过实验产生小鼠嵌合体;各种技术允许将不同的早期胚胎相互组合或与多能干细胞组合。在嵌合体中对不同谱系的后代进行鉴定,可用于跟踪细胞命运和功能,使基因型与表型相关联。小鼠嵌合体已成为研究关键发育过程的工具,包括细胞特化、分化、模式形成以及特定基因的功能。此外,还可以生成嵌合体来研究成年动物的生物学过程,包括疾病或组织修复和再生的机制。本文综述了不同类型的嵌合体及其生成方法,并举例说明了小鼠嵌合体如何提供一个独特而强大的系统来研究发育和成年生物体中细胞和组织功能的相关问题。