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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2014
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/18091
Title: | Suicide cells in normal and pathological |
Authors: | Bejenari, Inna |
Keywords: | apoptosis;programmed cell death |
Issue Date: | 2014 |
Publisher: | Ministry of Health of the Republic of Moldova, State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association |
Citation: | BEJENARI, Inna. Suicide cells in normal and pathological. In: MedEspera: the 5th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2014, pp. 30-31. |
Abstract: | Introduction: The cells of a multicellular organism are members of a highly organized community.
The number of cells in this community is highly regulated — not simply by controlling the rate of cell
division, but also by controlling the rate of cell death. If cells are no longer needed, they commit suicide by activating an intracellular death program. This process is called programmed cell death, or apoptosis (from a Greek word meaning “falling off,” as leaves from a tree). Apoptosis is a vital component of various
processes including normal cell turnover, proper development and functioning of the immune system,
hormone-dependent atrophy, embryonic development and chemical-induced cell death.
The purpose of this review is to provide a general overview of current knowledge on the
process of apoptosis, the role of apoptosis in health and disease, as well as a discussion of potential
alternative forms of apoptosis.
The mechanisms of apoptosis are highly complex, involving an energy-dependent cascade of
molecular events. Recent studies indicate that there are two main apoptotic pathways: the extrinsic
and the intrinsic. There is an additional pathway, that involves T-cell mediated cytotoxicity and
perforin-granzyme-dependent killing of the cell. The perforin/granzyme pathway can induce
apoptosis via either granzyme B or granzyme A. The extrinsic, intrinsic, and granzyme B pathways
converge to the same final, or execution pathway. This pathway is initiated by the cleavage of
caspase-3 and results in DNA fragmentation, degradation of cytoskeletal and nuclear proteins,
cross-linking of proteins, formation of apoptotic bodies, expression of ligands for phagocytic cell
receptors and finally uptake by phagocytic cells. Abnormalities in cell death regulation can be a
significant component of diseases such as cancer, autoimmune lymphoproliferative syndrome,
AIDS, ischemia, and neurodegenerative diseases such as Parkinson’s disease, Alzheimer’s disease,
Huntington’s disease, and Amyotrophic Lateral Sclerosis. Some conditions feature insufficient
apoptosis whereas others feature excessive apoptosis.
Conclusions: Apoptosis is a highly regulated energy-dependent process. The importance of
apoptosis consists in understanding its mechanism, because it is a vital component of health
maintenance and disease outbreak. The widespread involvement of apoptosis in the
pathophysiology of disease define studying the treatment strategies of that disease. Understanding
the mechanisms of apoptosis at the molecular level provides deeper insight into various disease
processes and may thus influence therapeutic strategy. |
metadata.dc.relation.ispartof: | MedEspera: The 5th International Medical Congress for Students and Young Doctors, May 14-17, 2014, Chisinau, Republic of Moldova |
URI: | http://repository.usmf.md/handle/20.500.12710/18091 |
Appears in Collections: | MedEspera 2014
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