Tuesday, 26 December 2017

48th Article " Matrix-Degrading metalloproteinasesin photoaging."


Nur fatmawati
16611047

Matrix-Degrading metalloproteinasesin photoaging.

In contrast to the results presented above, cell culture and skin equivalent model studies have concluded that dermal fibroblasts are the major source of MMPs that are expressed in response to UV irradiation. The reasons for the discrepancies between responses of human skin cells in vivoand responses of cultured skin cells in vitro are not known. However, there are many other examples of cultured skin cells failing to mimic the behavior of cells in vivo. Obviously, it is important to compare, whenever possible, results obtained from simple model systems with those obtained from direct in vivo observations Ultraviolet (UV) irradiation from the sun adversely impacts skin health through complex, multiple molecular pathways.Damage to the dermal connective tissue is a hallmark of photoaged skin. Disruption of the normal architecture of skin connective tissue impairs skin function and causes it to look aged. UV irradiation induces expression of certain members of the matrix metalloproteinase (MMP) family, which degrade collagen and other extracellular matrix (ECM).      

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