在单细胞生物和多细胞生物中进行编程细胞死亡.
Madhura Kulkarni1, J Marie Hardwick1,2
1W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA; email: mkulkar5@jhmi.edu, hardwick@jhu.edu.
Annual review of genetics
|September 18, 2023
概括
编程细胞死亡,或自我诱导的细胞死亡,在所有生命中都存在. 最近的研究揭示了细菌和真菌中古老的微生物死亡机制,为动物细胞死亡和免疫提供了新的见解.
科学领域:
- 细胞生物学 细胞生物学
- 微生物学 微生物学
- 免疫学 免疫学 免疫学
背景情况:
- 编程细胞死亡 (PCD) 是所有生命形式的基础,包括单细胞生物.
- 研究历史上一直集中在动物模型上,以了解疾病和发育.
- 最近的发现突显了细菌和真菌中古老的PCD机制,与免疫有关.
研究的目的:
- 审查PCD研究的历史发展,主要是从动物研究.
- 将新发现的微生物细胞死亡机制与哺乳动物细胞死亡机制进行比较和对比.
- 为了强调PCD在人类致病微生物中的研究不足的性质.
主要方法:
- 编程细胞死亡研究的文献综述.
- 哺乳动物,细菌和真菌细胞死亡途径的比较分析.
- 讨论进化起源和免疫系统的联系.
主要成果:
- 在细菌和真菌中发现了100多种微生物细胞死亡机制,与哺乳动物中的20个形成鲜明对比.
- 微生物PCD路径显示古代起源,并与免疫反应交织在一起.
- 在了解主要的人类病原性微生物PCD方面存在重大差距.
结论:
- 经过PCD研究的演变,从对动物的关注转向了对微生物的研究.
- 了解微生物PCD对于解决病原体带来的公共卫生挑战至关重要.
- 对比研究揭示了生命各个领域细胞死亡的保存和分化方面.
相关概念视频
Overview of Cell Death
7.4K
Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
7.4K
Necrosis
4.6K
Necrosis is considered as an “accidental” or unexpected form of cell death that ends in cell lysis. The first noticeable mention of “necrosis” was in 1859 when Rudolf Virchow used this term to describe advanced tissue breakdown in his compilation titled “Cell Pathology”.
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
4.6K
Apoptosis
11.6K
Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
11.6K
Autophagic Cell Death
3.4K
Christian de Duve discovered “autophagy,” a process in which cellular components are engulfed by membrane-bound organelles called autophagosomes. The autophagosomes then fuse with lysosomes to digest the enclosed contents. Autophagy is generally activated in cells to prevent cell death. However, cell death is triggered when the damage is beyond repair.
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
3.4K
Caspases
12.6K
Caspase, a family of cysteine proteases, serve as effectors in apoptosis. The ced3 gene in C.elegans was first identified to be involved in apoptosis. This gene encodes the ced-3 caspase that is similar to the interleukin-1-beta converting enzyme or ICE in mammals. In addition to apoptosis, caspases also function in the inflammatory response. Inflammatory caspases are essential in activating pro-inflammatory cytokines that recruit immune cells and block the replication of pathogens inside...
12.6K
Mitogens and the Cell Cycle
6.5K
Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
6.5K


