Molecular aspects of skin ageing

EC Naylor, REB Watson, MJ Sherratt - Maturitas, 2011 - Elsevier
Ageing of human skin may result from both the passage of time (intrinsic ageing) and from
cumulative exposure to external influences (extrinsic ageing) such as ultraviolet radiation …

Elastic fibres

CM Kielty, MJ Sherratt… - Journal of cell …, 2002 - journals.biologists.com
Elastic fibres are essential extracellular matrix macromolecules comprising an elastin core
surrounded by a mantle of fibrillin-rich microfibrils. They endow connective tissues such as …

Latent TGF-β binding proteins: extracellular matrix association and roles in TGF-β activation

M Hyytiäinen, C Penttinen… - Critical reviews in clinical …, 2004 - Taylor & Francis
Transforming growth factor betas (TGF-βs) are multifunctional and pleiotropic growth factors.
Their major effects include inhibition of cell proliferation and enhancement of extracellular …

The molecular genetics of Marfan syndrome and related microfibrillopathies

PN Robinson, M Godfrey - Journal of medical genetics, 2000 - jmg.bmj.com
Mutations in the gene for fibrillin-1 (FBN1) have been shown to cause Marfan syndrome, an
autosomal dominant disorder of connective tissue characterised by pleiotropic …

Fibrillin degradation by matrix metalloproteinases: implications for connective tissue remodelling

JL Ashworth, G Murphy, MJ Rock… - Biochemical …, 1999 - portlandpress.com
Fibrillin is the principal structural component of the 10-12 nm diameter elastic microfibrils of
the extracellular matrix. We have previously shown that both fibrillin molecules and …

Latent transforming growth factor-β binding proteins (LTBPs)—structural extracellular matrix proteins for targeting TGF-β action

J Saharinen, M Hyytiäinen, J Taipale… - Cytokine & growth factor …, 1999 - Elsevier
Growth factors of the transforming growth factor-β family are potent regulators of the
extracellular matrix formation, in addition to their immunomodulatory and regulatory roles for …

Anti-TGF-β treatment prevents skin and lung fibrosis in murine sclerodermatous graft-versus-host disease: a model for human scleroderma

LL McCormick, Y Zhang, E Tootell… - The Journal of …, 1999 - journals.aai.org
Scleroderma, a debilitating acquired connective tissue disease, is characterized by fibrosis,
particularly of the skin and lungs. Monocyte-produced TGF-β1, a potent stimulus for collagen …

Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome

BL Loeys, EE Gerber, D Riegert-Johnson… - Science translational …, 2010 - science.org
The predisposition for scleroderma, defined as fibrosis and hardening of the skin, is poorly
understood. We report that stiff skin syndrome (SSS), an autosomal dominant congenital …

Sialidases in vertebrates: a family of enzymes tailored for several cell functions

E Monti, E Bonten, A D'Azzo, R Bresciani… - Advances in …, 2010 - Elsevier
A bstract This review summarizes the recent research development on vertebrate sialidase
biology. Sialic acid-containing compounds play important roles in many physiological …

CD19-dependent B lymphocyte signaling thresholds influence skin fibrosis and autoimmunity in the tight-skin mouse

E Saito, M Fujimoto, M Hasegawa, K Komura… - The Journal of clinical …, 2002 - jci.org
The tight-skin (TSK/+) mouse, a genetic model for human systemic sclerosis (SSc), develops
cutaneous fibrosis and autoantibodies against SSc-specific target autoantigens. Although …