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  2. Cellular senescence - Wikipedia

    en.wikipedia.org/wiki/Cellular_senescence

    Cellular senescence is not observed in some organisms, including perennial plants, sponges, corals, and lobsters. In other organisms, where cellular senescence is observed, cells eventually become post-mitotic: they can no longer replicate themselves through the process of cellular mitosis (i.e., cells

  3. Tissue remodeling - Wikipedia

    en.wikipedia.org/wiki/Tissue_remodeling

    Programmed cellular senescence contributes to beneficial tissue remodeling during embryonic development of the fetus. [4] In a brain stroke the penumbra area surrounding the ischemic event initially undergoes a damaging remodeling, but later transitions to a tissue remodeling characterized by repair. [5]

  4. Senescence-associated secretory phenotype - Wikipedia

    en.wikipedia.org/wiki/Senescence-associated...

    Tumor necrosis factor (TNF) is increased 32-fold in stress-induced senescence, 8-fold in replicative senescence, and only slightly in proteosome-inhibited senescence. [9] Interleukin 6 (IL-6) and interleukin 8 (IL-8) are the most conserved and robust features of SASP. [10] But some SASP components are anti-inflammatory. [11]

  5. Hallmarks of aging - Wikipedia

    en.wikipedia.org/wiki/Hallmarks_of_aging

    This is called cellular senescence. Senescence can be induced by several factors, including telomere shortening, [37] DNA damage [38] and stress. Since the immune system is programmed to seek out and eliminate senescent cells, [39] it might be that senescence is one way for the body to rid itself of cells damaged beyond repair.

  6. Cholinergic anti-inflammatory pathway - Wikipedia

    en.wikipedia.org/wiki/Cholinergic_anti...

    Thus, the prefrontal input to the ANS modulate the inflammatory response to psychological stress in part via the cholinergic anti-inflammatory pathway. [14] In recent years, this PFC-Vagus Nerve-Spleen axis has been linked to cellular senescence [15] [16] and various pathologies such as neurodegenerative diseases and cancer. [17] [18]

  7. Fibrosis - Wikipedia

    en.wikipedia.org/wiki/Fibrosis

    Fibrosis can occur in many tissues within the body, typically as a result of inflammation or damage. Common sites of fibrosis include the lungs, liver, kidneys, brain, and heart: Micrograph showing cirrhosis of the liver. The tissue in this example is stained with a trichrome stain, in which fibrosis is colored blue.

  8. Senescence - Wikipedia

    en.wikipedia.org/wiki/Senescence

    Senescence (/ s ɪ ˈ n ɛ s ə n s /) or biological aging is the gradual deterioration of functional characteristics in living organisms. Whole organism senescence involves an increase in death rates or a decrease in fecundity with increasing age, at least in the later part of an organism's life cycle.

  9. Cell death - Wikipedia

    en.wikipedia.org/wiki/Cell_death

    Overview of signal transduction pathways involved in apoptosis. Cell death is the event of a biological cell ceasing to carry out its functions. This may be the result of the natural process of old cells dying and being replaced by new ones, as in programmed cell death, or may result from factors such as diseases, localized injury, or the death of the organism of which the cells are part.