无积体症会影响哺乳动物细胞的增殖和自发不朽化
Bret R Williams1, Vineet R Prabhu, Karen E Hunter
1David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.
概括
积体,或错误的染色体数量,损害了细胞生长和新陈代谢. 这项研究揭示,体积症降低了细胞的健康状况,并导致不同体细胞共享的特征,影响生物和细胞.
科学领域:
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
- 癌症研究 癌症研究
背景情况:
- 染色体数异常 (aneuploidy) 与流产,智力障碍和癌症有关.
- 了解形积分病的细胞效应对于人类健康和疾病研究至关重要.
研究的目的:
- 为了研究形积分症对初级小鼠细胞增殖,新陈代谢和不朽化的影响.
- 为了确定形形状是否影响细胞健康,并诱导不同形状细胞类型的共同特征.
主要方法:
- 产生具有四种特定染色体之一 (三体线) 额外副本的小鼠细胞系.
- 分析这些无体细胞系的增殖率,代谢特性和永生能力.
主要成果:
- 所有四个三体细胞系都表现出受损的增殖.
- 形细胞的代谢特性发生了显著的改变.
- 细胞实现无限期增殖 (不朽化) 的能力受到额外的染色体副本的影响.
结论:
- 形积分症降低了细胞的健康状况,影响了基本的生物过程.
- 体细胞具有共同的特征,无论涉及哪种特定的染色体.
- 这些发现凸显了细胞水平上形积分症的有害影响,对发育和疾病有影响.
相关概念视频
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...
Nondisjunction
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Abnormal Proliferation
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
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...
Molecular Factors Affecting Cell Division
Several external and internal factors influence the initiation and inhibition of cell division. For instance, the death of nearby cells or the release of human growth hormone (hGH) promotes cell division. In contrast, lack of hGH or crowding of cells can inhibit cell division.
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
Cell Lines
A cell line is a population of cells grown in vitro that can be subcultured over several generations. Normal cells cease to divide after a certain number of cell divisions, a process known as replicative senescence. This number, called the Hayflick limit, was conceptualized by Leonard Hayflick in 1961 when he observed that fetal cells grown in culture could only divide 40-60 times. This limit is due to the shortening of the telomeres during each round of cell division, preventing cell division...


