Apoptosis
(Redirected from Proapoptotic)
Apoptosis, commonly referred to as programmed cell death, is a crucial biological process that orchestrates the deliberate elimination of cells in multicellular organisms. This intrinsically regulated mechanism facilitates the maintenance of cellular homeostasis, development, and proper immune system function, among other vital roles. Distinct from necrosis and other forms of cell death, apoptosis is marked by unique morphological and biochemical hallmarks.
Etymology[edit | edit source]
The term "apoptosis" (απόπτωσις) originates from the Greek language, signifying the "falling off" or "dropping off" of petals from flowers or leaves from trees, metaphorically capturing the process by which cells are purposefully removed from an organism.
Biochemical and Morphological Characteristics[edit | edit source]
Apoptotic cells exhibit several distinguishing characteristics:
- Cell Shrinkage: The cell undergoes a reduction in volume.
- Chromatin Condensation: Genetic material becomes densely packed.
- Formation of Apoptotic Bodies: The cell's fragments are contained in vesicles.
- Phosphatidylserine Exposure: Once confined to the inner leaflet of the plasma membrane, phosphatidylserine translocates to the cell surface.
On a biochemical level, apoptosis is often accompanied by:
- Caspase activation: Caspases, a family of cysteine proteases, play a pivotal role in mediating the apoptotic process.
- DNA fragmentation: DNA undergoes cleavage at inter-nucleosomal regions.
- Mitochondrial Changes: Including the release of cytochrome c.
Signaling Pathways[edit | edit source]
Apoptosis can be initiated via two primary pathways:
Intrinsic Pathway (Mitochondrial): Triggered by internal signals, often as a result of DNA damage or oxidative stress. Characterized by mitochondrial outer membrane permeabilization (MOMP), leading to cytochrome c release. Extrinsic Pathway (Death Receptor): Initiated by extracellular ligands binding to cell-surface death receptors. Leads to formation of the death-inducing signaling complex (DISC) and subsequent caspase-8 activation. Both pathways converge on a shared execution phase, resulting in caspase-3 activation and the eventual demise of the cell.
Physiological Roles[edit | edit source]
Apoptosis serves numerous essential roles in physiology, including:
- Development: Shaping of organs, removal of transient structures, and regulation of cell numbers.
- Homeostasis: Maintaining equilibrium by controlling cell numbers.
- Immune System Function: Removal of autoreactive cells and aiding immune cell maturation.
Pathological Implications[edit | edit source]
Defective or excessive apoptosis can have pathological implications:
- Cancer: Impaired apoptosis can contribute to tumor genesis and resistance to therapy.
- Neurodegenerative diseases: Excessive neuronal apoptosis is implicated in conditions like Alzheimer's and Parkinson's.
- Autoimmune disorders: Due to failed removal of self-reactive immune cells.
Summary[edit | edit source]
Apoptosis is an evolutionarily conserved mechanism indispensable for the development and maintenance of cellular integrity in multicellular organisms. Understanding its intricate regulation and diverse roles is critical in therapeutic contexts, especially in the realm of oncology, neurology, and immunology.
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Contributors: Prab R. Tumpati, MD