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      Hyaluronic acid: A key molecule in skin aging

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          Abstract

          Skin aging is a multifactorial process consisting of two distinct and independent mechanisms: intrinsic and extrinsic aging. Youthful skin retains its turgor, resilience and pliability, among others, due to its high content of water. Daily external injury, in addition to the normal process of aging, causes loss of moisture. The key molecule involved in skin moisture is hyaluronic acid (HA) that has unique capacity in retaining water. There are multiple sites for the control of HA synthesis, deposition, cell and protein association and degradation, reflecting the complexity of HA metabolism. The enzymes that synthesize or catabolize HA and HA receptors responsible for many of the functions of HA are all multigene families with distinct patterns of tissue expression. Understanding the metabolism of HA in the different layers of the skin and the interactions of HA with other skin components will facilitate the ability to modulate skin moisture in a rational manner.

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          Most cited references97

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          Hyaluronan as an immune regulator in human diseases.

          Accumulation and turnover of extracellular matrix components are the hallmarks of tissue injury. Fragmented hyaluronan stimulates the expression of inflammatory genes by a variety of immune cells at the injury site. Hyaluronan binds to a number of cell surface proteins on various cell types. Hyaluronan fragments signal through both Toll-like receptor (TLR) 4 and TLR2 as well as CD44 to stimulate inflammatory genes in inflammatory cells. Hyaluronan is also present on the cell surface of epithelial cells and provides protection against tissue damage from the environment by interacting with TLR2 and TLR4. Hyaluronan and hyaluronan-binding proteins regulate inflammation, tissue injury, and repair through regulating inflammatory cell recruitment, release of inflammatory cytokines, and cell migration. This review focuses on the role of hyaluronan as an immune regulator in human diseases.
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            Hyaluronidases: their genomics, structures, and mechanisms of action.

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              Angiogenesis induced by degradation products of hyaluronic acid.

              Partial degradation products of sodium hyaluronate produced by the action of testicular hyaluronidase induced an angiogenic response (formation of new blood vessels) on the chick chorioallantoic membrane. Neither macromolecular hyaluronate nor exhaustively digested material had any angiogenic potential. Fractionation of the digestion products established that the activity was restricted to hyaluronate fragments between 4 and 25 disaccharides in length.
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                Author and article information

                Journal
                Dermatoendocrinol
                Dermatoendocrinol
                DERM
                Dermato-endocrinology
                Landes Bioscience
                1938-1972
                1938-1980
                01 July 2012
                01 July 2012
                : 4
                : 3
                : 253-258
                Affiliations
                [1 ]Department of Pharmacology; School of Medicine; Aristotle University of Thessaloniki; Thessaloniki, Greece
                [2 ]Pulmonary Cell Research-Pneumology; University Hospital Basel; Basel, Switzerland
                Author notes
                [* ]Correspondence to: George Karakiulakis, Email: gkaraki@ 123456med.auth.gr
                Article
                2012DE0197R 21923
                10.4161/derm.21923
                3583886
                23467280
                180d680c-87b7-4969-ad81-3092cbc737fb
                Copyright © 2012 Landes Bioscience

                This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.

                History
                Categories
                Review

                Dermatology
                rhamm,cd44,hyaluronic acid,hyaluronidases,skin aging,hyaluronic acid synthases
                Dermatology
                rhamm, cd44, hyaluronic acid, hyaluronidases, skin aging, hyaluronic acid synthases

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