Programmed cell death (PCD; sometimes referred to as cellular suicide) is the death of a cell as a result of events inside of a cell, such as apoptosis or autophagy. PCD is carried out in a biological process, which usually confers advantage during an organism's lifecycle. For example, the differentiation of fingers and toes in a developing human embryo occurs because cells between the fingers apoptose; the result is that the digits are separate. PCD serves fundamental functions during both plant and animal tissue development.
Apoptosis and autophagy are both forms of programmed cell death. Necrosis is the death of a cell caused by external factors such as trauma or infection and occurs in several different forms. Necrosis was long seen as a non-physiological process that occurs as a result of infection or injury, but in the 2000s, a form of programmed necrosis, called necroptosis, was recognized as an alternative form of programmed cell death. It is hypothesized that necroptosis can serve as a cell-death backup to apoptosis when the apoptosis signaling is blocked by endogenous or exogenous factors such as viruses or mutations. Most recently, other types of regulated necrosis have been discovered as well, which share several signaling events with necroptosis and apoptosis.
The concept of "programmed cell-death" was used by Lockshin & Williams in 1964 in relation to insect tissue development, around eight years before "apoptosis" was coined. The term PCD has, however, been a source of confusion and Durand and Ramsey have developed the concept by providing mechanistic and evolutionary definitions. PCD has become the general terms that refers to all the different types of cell death that have a genetic component.
The first insight into the mechanism came from studying BCL2, the product of a putative oncogene activated by chromosome translocations often found in follicular lymphoma. Unlike other cancer genes, which promote cancer by stimulating cell proliferation, BCL2 promoted cancer by stopping lymphoma cells from being able to kill themselves.
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This course is aimed to familiarize students with the 3D organization of a eukaryotic cell, its compartmentalization, how cellular compartments communicate together and how a cell communicates with it
The course covers in detail molecular mechanisms of cancer development with emphasis on cell cycle control, genome stability, oncogenes and tumor suppressor genes.
The course covers in detail the interactions of cancer cells with their environment with an emphasis on tumor-angiogenesis, inflammation, adaptive and innate immunity and cancer-induced immune suppres
Les maladies neurodégénératives, telles que la maladie d'Alzheimer, la maladie à corps de Lewy, la maladie de Parkinson, la maladie de Huntington, l'atrophie corticale postérieure ou encore la sclérose latérale amyotrophique sont des maladies chroniques invalidantes à évolution lente et discrète. Elles provoquent généralement une détérioration du fonctionnement des cellules nerveuses, en particulier les neurones, pouvant conduire à la mort cellulaire (ou neurodégénérescence).
Les caspases sont une classe de protéases à cystéine qui reconnaissent chacune une séquence particulière sur certaines protéines et hydrolysent la liaison peptidique côté carboxyle d'un résidu d'aspartate de cette séquence. Ces enzymes jouent un rôle essentiel dans les phénomènes inflammatoires ainsi que dans l'apoptose (mort cellulaire programmée) et la nécrose. Le terme « caspase » est la contraction en anglais de l'expression cysteine-aspartic protease, parfois également écrite cysteine-dependent aspartate-directed protease, voire cysteinyl-aspartate-cleaving protease.
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Discute des phénotypes LGR5 chez la souris et des techniques d'analyse de lignée.
Explore les mécanismes de mort cellulaire programmée, y compris l'apoptose et l'autophagie, en mettant l'accent sur leurs implications dans divers organismes et processus de régénération.
Explore la régulation de l'apoptose, l'impact sur les tumeurs, les voies de signalisation de la survie, l'autophagie dans le cancer et les défis du ciblage mTOR.
Time-lapse light microscopy combined with in vitro neuronal cultures has provided a significant contribution to the field of Developmental Neuroscience. The establishment of the neuronal polarity, i.e., formation of axons and dendrites, key structures resp ...
The endoplasmic reticulum (ER) extends to the outer (ONM) and the inner (INM) nuclear membrane forming the nuclear envelope (NE) that delimits the nucleoplasm containing the cell genome. Unfolded protein responses (UPRs) and reticulophagy responses increas ...
A series of Ga(Q(n))(3) coordination compounds have been synthesized, where HQ(n) is 1-phenyl-3-methyl-4-RC(=O)-pyrazolo-5-one. The complexes have been characterized through analytical data, NMR and IR spectroscopy, ESI mass spectrometry, elemental analysi ...