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1.
Aging Cell ; 11(4): 722-5, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22612594

ABSTRACT

Cellular senescence is a defense mechanism in response to molecular damage which accumulates with aging. Correspondingly, the number of senescent cells has been reported to be greater in older than in younger subjects and furthermore associates with age-related pathologies. Inter-individual differences exist in the rate at which a person ages (biological age). Here, we studied whether younger biological age is related to fewer senescent cells in middle-aged individuals with the propensity for longevity, using p16INK4a as a marker for cellular senescence. We observed that a younger biological age associates with lower levels of p16INK4a positive cells in human skin.


Subject(s)
Aging/metabolism , Aging/pathology , Cyclin-Dependent Kinase Inhibitor p16/metabolism , Skin/cytology , Skin/metabolism , Aged , Aged, 80 and over , Biomarkers/metabolism , Cell Count , Cellular Senescence/physiology , Epidermal Cells , Epidermis/metabolism , Female , Fibroblasts/cytology , Fibroblasts/metabolism , Humans , Longevity/physiology , Male , Middle Aged , Skin Aging/physiology
2.
PLoS One ; 4(12): e8021, 2009 Dec 01.
Article in English | MEDLINE | ID: mdl-19956599

ABSTRACT

The desire of many to look young for their age has led to the establishment of a large cosmetics industry. However, the features of appearance that primarily determine how old women look for their age and whether genetic or environmental factors predominately influence such features are largely unknown. We studied the facial appearance of 102 pairs of female Danish twins aged 59 to 81 as well as 162 British females aged 45 to 75. Skin wrinkling, hair graying and lip height were significantly and independently associated with how old the women looked for their age. The appearance of facial sun-damage was also found to be significantly correlated to how old women look for their age and was primarily due to its commonality with the appearance of skin wrinkles. There was also considerable variation in the perceived age data that was unaccounted for. Composite facial images created from women who looked young or old for their age indicated that the structure of subcutaneous tissue was partly responsible. Heritability analyses of the appearance features revealed that perceived age, pigmented age spots, skin wrinkles and the appearance of sun-damage were influenced more or less equally by genetic and environmental factors. Hair graying, recession of hair from the forehead and lip height were influenced mainly by genetic factors whereas environmental factors influenced hair thinning. These findings indicate that women who look young for their age have large lips, avoid sun-exposure and possess genetic factors that protect against the development of gray hair and skin wrinkles. The findings also demonstrate that perceived age is a better biomarker of skin, hair and facial aging than chronological age.


Subject(s)
Aging/physiology , Skin Aging/physiology , Aged , Aged, 80 and over , Aging/genetics , Biomarkers/metabolism , Denmark , Environment , Face/anatomy & histology , Female , Hair/growth & development , Hair/physiology , Humans , Inheritance Patterns/genetics , Linear Models , Middle Aged , Reproducibility of Results , Siblings , Skin Aging/genetics , United Kingdom
3.
J Nutr Biochem ; 20(10): 806-15, 2009 Oct.
Article in English | MEDLINE | ID: mdl-18926687

ABSTRACT

The ethyl acetate extract of the gum of the guggul tree, Commiphora mukul (guggulipid), is marketed for the treatment of dyslipidaemia and obesity. We have found that it protects Lep(ob)/Lep(ob) mice from diabetes and have investigated possible molecular mechanisms for its metabolic effects, in particular those due to a newly identified component, commipheric acid. Both guggulipid (EC(50)=0.82 microg/ml) and commipheric acid (EC(50)=0.26 microg/ml) activated human peroxisome proliferator-activated receptor alpha (PPARalpha) in COS-7 cells transiently transfected with the receptor and a reporter gene construct. Similarly, both guggulipid (EC(50)=2.3 microg/ml) and commipheric acid (EC(50)=0.3 microg/ml) activated PPARgamma and both promoted the differentiation of 3T3 L1 preadipocytes to adipocytes. Guggulipid (EC(50)=0.66 microg/ml), but not commipheric acid, activated liver X receptor alpha (LXRalpha). E- and Z-guggulsterones, which are largely responsible for guggulipid's hypocholesterolaemic effect, had no effects in these assays. Guggulipid (20 g/kg diet) improved glucose tolerance in female Lep(ob)/Lep(ob) mice. Pure commipheric acid, given orally (960 mg/kg body weight, once daily), increased liver weight but did not affect body weight or glucose tolerance. However, the ethyl ester of commipheric acid (150 mg/kg, twice daily) lowered fasting blood glucose and plasma insulin, and plasma triglycerides without affecting food intake or body weight. These results raise the possibility that guggulipid has anti-diabetic activity due partly to commipheric acid's PPARalpha/gamma agonism, but the systemic bioavailability of orally dosed, pure commipheric acid appears poor. Another component may contribute to guggulipid's anti-diabetic and hypocholesterolaemic activity by stimulating LXRalpha.


Subject(s)
Hypoglycemic Agents/pharmacology , Leptin/physiology , PPAR alpha/agonists , PPAR gamma/agonists , Plant Extracts/pharmacology , Plant Gums/pharmacology , 3T3-L1 Cells , Adipocytes/cytology , Adipocytes/drug effects , Animals , Base Sequence , COS Cells , Cell Differentiation/drug effects , Chlorocebus aethiops , Commiphora , DNA Primers , Female , Humans , Insulin Resistance , Leptin/genetics , Mice , Mice, Inbred C57BL , Obesity/genetics
4.
Plant J ; 38(1): 27-37, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15053757

ABSTRACT

Xyloglucan-acting enzymes are believed to have effects on type I primary plant cell wall mechanical properties. In order to get a better understanding of these effects, a range of enzymes with different in vitro modes of action were tested against cell wall analogues (bio-composite materials based on Acetobacter xylinus cellulose and xyloglucan). Tomato pericarp xyloglucan endo transglycosylase (tXET) and nasturtium seed xyloglucanase (nXGase) were produced heterologously in Pichia pastoris. Their action against the cell wall analogues was compared with that of a commercial preparation of Trichoderma endo-glucanase (EndoGase). Both 'hydrolytic' enzymes (nXGase and EndoGase) were able to depolymerise not only the cross-link xyloglucan fraction but also the surface-bound fraction. Consequent major changes in cellulose fibril architecture were observed. In mechanical terms, removal of xyloglucan cross-links from composites resulted in increased stiffness (at high strain) and decreased visco-elasticity with similar extensibility. On the other hand, true transglycosylase activity (tXET) did not affect the cellulose/xyloglucan ratio. No change in composite stiffness or extensibility resulted, but a significant increase in creep behaviour was observed in the presence of active tXET. These results provide direct in vitro evidence for the involvement of cell wall xyloglucan-specific enzymes in mechanical changes underlying plant cell wall re-modelling and growth processes. Mechanical consequences of tXET action are shown to be complimentary to those of cucumber expansin.


Subject(s)
Cellulose/metabolism , Glucans/metabolism , Glycoside Hydrolases/metabolism , Glycosyltransferases/metabolism , Solanum lycopersicum/enzymology , Tropaeolum/enzymology , Xylans/metabolism , Base Sequence , Biomechanical Phenomena , Cell Wall/enzymology , Cellulose/chemistry , Cellulose/ultrastructure , Cross-Linking Reagents , DNA, Plant/genetics , Elasticity , Glucans/chemistry , Glucans/ultrastructure , Glycoside Hydrolases/genetics , Glycosyltransferases/genetics , Hydrolysis , Solanum lycopersicum/genetics , Microscopy, Electron , Pichia/genetics , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Tropaeolum/genetics , Viscosity , Xylans/chemistry , Xylans/ultrastructure
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