相关实验视频
Updated: Jul 11, 2026

12:08
Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
Published on: May 22, 2013
通过将端粒酶引入正常人体细胞,延长寿命
A G Bodnar1, M Ouellette, M Frolkis
1Geron Corporation, Menlo Park, CA 94025, USA.
概括
细胞衰老,一个有限的细胞分裂极限,是由端粒缩短触发的. 引入端粒酶抵消了这一点,延长了端粒并防止了人类细胞的衰老,证明了端粒长度控制了细胞衰老.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 正常的人类细胞有有限数量的分裂,进入复制性衰老.
- 假设端粒缩短是触发衰老的分子钟.
研究的目的:
- 为了研究端粒缩短和细胞衰老之间的因果关系.
- 为了确定端粒酶是否可以预防或逆转正常人体细胞的衰老.
主要方法:
- 用编码人类端粒酶催化子单元的载体感染两个端粒酶阴性正常人体细胞类型 (视网膜色素上皮细胞和前皮纤维细胞).
- 端粒酶表达克隆与端粒酶负控克隆的比较,涉及端粒长度,细胞分裂和衰老标记 (β-galactosidase染色).
主要成果:
- 表达端粒酶的克隆表现出延长的端粒和强烈的细胞分裂,而不是控制克隆的缩短的端粒和衰老.
- 在端粒酶表达细胞中减少β-galactosidase染色表明延迟或预防衰老.
- 表达端粒酶的克隆保持正常的型,并至少超过了20倍的正常寿命.
结论:
- 建立了端粒缩短和体外细胞衰老之间的因果关系.
- 证明端粒酶可以保持正常的人类细胞在表型年轻的状态.
- 突出了端粒酶在研究和医学中的潜在应用,以促进细胞寿命.
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10:14Telomerase Activity in the Various Regions of Mouse Brain: Non-Radioactive Telomerase Repeat Amplification Protocol (TRAP) Assay
Published on: September 2, 2014
08:34Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer
Published on: April 13, 2015
相关概念视频
Replication in Eukaryotes
Overview
Telomeres and Telomerase
In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded DNA.
Replicative Cell Senescence
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
Replication in Eukaryotes
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
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Eukaryotic replication follows many of the same...
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
Telomeres and Telomerase
In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded DNA.
Replicative Cell Senescence
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...