Serum and granulocyte elastase-type protease activities were determined simultaneously with their main plasma proteinase inhibitors such as alpha-1-antitrypsin and alpha-2-macroglobulin in healthy control and atherosclerotic (ATS) subjects. The age-related associations of these parameters were also investigated. Serum elastase-type protease activity increased, but not statistically significantly, with aging in both control and ATS subjects. The enhancement of elastase-type protease activity in sera of ATS patients was significantly (p less than .02) greater than control subjects only in the case of the elderly. The granulocytes' elastase activity was significantly greater in granulocytes derived from both middle-aged and elderly ATS patients (p less than .03 and p less than .06) compared to age-matched control subjects. Alpha-1-antitrypsin was not significantly lower, whereas alpha-2-macroglobulin was significantly lower in sera of ATS subjects compared to age-matched control subjects (p less than .01). The conclusion is that increased elastase-type activity and decreased antiproteinase activity should be considered as potential factors in atherosclerotic arterial wall damage. The similarity of the results in the elderly and the ATS subjects suggest that atherosclerosis is an early aging process.
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http://dx.doi.org/10.1093/geronj/47.5.b154 | DOI Listing |
Fungal Biol
February 2025
Department of Microbiology and Virology, Faculty of Biology, University of Havana, San Lázaro & L, Vedado, Havana, Cuba. Electronic address:
The aim of this work is to evaluate different molecular strategies deployed by indigenous isolates of Trichoderma in their interaction with the phytopathogen Botrytis cinerea. In vitro antagonism assays, determination of volatile and diffusible compounds, and the relative expression of the prb1 gene, which codes for an extracellular protease, before and during the stage of direct contact between the two fungi, were carried out; the characterization of this protease was also performed. All 17 Trichoderma strains tested showed high levels of inhibition against B.
View Article and Find Full Text PDFJ Biosci
March 2019
Department of Microbiology and Botany, Faculty of Science, Zagazig University, Zagazig 44519, Egypt,
A 48 kDa ZuhP13 elastase from P. aeruginosa isolated from a urine sample was successfully purified to 8.8-fold and 39% recovery by DEAE-Sepharose CL-6B and Sephadex G-100 chromatography.
View Article and Find Full Text PDFArch Gerontol Geriatr
June 2010
Laboratoire de recherche ophtalmologique, Hôpital Hôtel Dieu, Université Paris V-1, place du Parvis Notre Dame, F-75181 Paris cedex 04, France.
It could be shown using the in vitro cell culture aging model, that elastase-type endopeptidase activity is progressively upregulated with successive passages (in vitro aging). Similar results were obtained previously by determining elastase-type activity as a function of age in aorta extracts (human) and skin extracts (mouse). Among the possible mechanisms involved we tested the role of advanced glycation endproducts (AGEs) on this process.
View Article and Find Full Text PDFPlant Physiol
March 2008
Centre for Forest Biology and Department of Biology, University of Victoria, Victoria, BC, Canada.
We investigated the functional and biochemical variability of Kunitz trypsin inhibitor (KTI) genes of Populus trichocarpa x Populus deltoides. Phylogenetic analysis, expressed sequence tag databases, and western-blot analysis confirmed that these genes belong to a large and diverse gene family with complex expression patterns. Five wound- and herbivore-induced genes representing the diversity of the KTI gene family were selected for functional analysis and shown to produce active KTI proteins in Escherichia coli.
View Article and Find Full Text PDFJ Cell Physiol
December 2007
Laboratory of Applied Genetics, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Whey acidic protein (WAP) is a major whey protein in milk that has structural similarity to the family of serine protease inhibitors with WAP motif domains characterized by a four-disulfide core. We previously reported that enforced expression of the mouse WAP transgene in mammary epithelial cells inhibits their proliferation in vitro and in vivo by means of suppressing cyclin D1 expression (Nukumi et al., 2004, Dev Biol 274: 31-44).
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