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1.
Arteriosclerosis ; 9(4): 550-9, 1989.
Article in English | MEDLINE | ID: mdl-2473734

ABSTRACT

The endothelium controls the influx of lipoproteins into the arterial wall, a process that may be disturbed in arteriosclerotic blood vessels. We have used an in vitro model to investigate the characteristics of the passage of low density lipoproteins (LDL) through monolayers of human arterial endothelial cells. Umbilical artery, aorta, or carotid artery endothelial cells were cultured on polycarbonate filters and formed a tight monolayer in which the cells were connected by tight junctions. Passage of 125I-LDL through these monolayers proceeded linearly over a 24-hour period. It was threefold lower through monolayers of aorta or carotid artery cells than through monolayers of umbilical artery cells. The LDL passage process did not show saturation with LDL concentrations up to 800 micrograms/ml LDL-protein (i.e., 1.6 nmol/ml apolipoprotein B) between 2 and 4 hours after addition. However, during the first 30 to 60 minutes after addition of high concentrations of LDL, a reduction of the passage rate of both LDL and peroxidase, resulting in an apparent saturation of the passage process, was observed. The passage rate of the negatively charged acetylated LDL was twofold lower than that of native LDL. Addition of histamine to the endothelial monolayer resulted in a large, but transient, increase in permeability paralleled by a decrease in electrical resistance. The effects of histamine were mediated via an H1 receptor. Thrombin and Ca++ ionophore also induced an increase in permeability of the monolayer, while bradykinin did not. The effects of histamine and thrombin were paralleled by a rapid and marked increase in cytoplasmatic Ca++ concentration of the endothelial cells, while bradykinin induced only a small increase. Although the cyclic adenosine 5'-monophosphate-elevating agent, forskolin, markedly decreased the basal rate of LDL passage through the endothelial cell monolayers, it did not change the relative increase in permeability induced by histamine. Thus, histamine induces small, but significant, increases in the permeability of tight endothelial cell monolayers.


Subject(s)
Bradykinin/pharmacology , Calcium/pharmacology , Endothelium, Vascular/metabolism , Histamine/pharmacology , Lipoproteins, LDL/metabolism , Thrombin/pharmacology , 1-Methyl-3-isobutylxanthine/pharmacology , Aorta , Calcium/metabolism , Capillary Permeability/drug effects , Carotid Arteries , Cells, Cultured , Colforsin/pharmacology , Cyclic AMP/metabolism , Electric Conductivity , Endothelium, Vascular/cytology , Humans , Iodine Radioisotopes , Umbilical Arteries
2.
Eur J Cell Biol ; 48(1): 27-36, 1989 Feb.
Article in English | MEDLINE | ID: mdl-2743992

ABSTRACT

A postembedding labeling technique was employed to visualize human native low density lipoproteins (LDL) during transcytosis in rat arterial endothelium. For this purpose human LDL was perfused through rat vasculature before fixation and processing for immunoelectron microscopy. The LDL particles were located on sections by anti-human apolipoprotein B-100 (LDL) antibodies and secondary antibodies or protein-A conjugated to 10-nm colloidal gold. LDL molecules were seen in plasmalemmal vesicles as well as in the subendothelial space. No colloidal gold was found in the intercellular junctions. Perfusion with reductively methylated LDL, which cannot bind to the LDL receptor, gave a similar labeling pattern, indicating that transcytosis of LDL via plasmalemmal vesicles is most likely receptor independent. Furthermore, the passage of LDL through intact vascular endothelium is a vesicular transport rather than an intercellular diffusion process.


Subject(s)
Arteries/metabolism , Lipoproteins, LDL/metabolism , Animals , Arteries/cytology , Arteries/ultrastructure , Endothelium, Vascular/metabolism , Endothelium, Vascular/ultrastructure , Humans , Immunohistochemistry , Male , Microscopy, Electron/methods , Perfusion , Rats , Rats, Inbred Strains , Receptors, LH/metabolism , Receptors, LH/physiology
3.
Pak Dev Rev ; 25(4): 609-26, 1986.
Article in English | MEDLINE | ID: mdl-12341746

ABSTRACT

PIP: This article studies how people become upwardly mobile, or the factors involved in this process, in Pakistan. It explains the income and wealth positions of Pakistanis from different generations in terms of their endowments of social, human, and physical capital and other socioeconomic characteristics. 1200 respondents from 10 major city districts were interviewed in 1982. The analysis of correlations between the absolute level of income and wealth vis-a-vis the fathers' and sons' characteristics has shown that the improvement in the economic position of sons follows a more stable and coherent pattern than the improvement in fathers' economic position. The analysis of the magnitudes of mobility indicators shows that the dispersion of accumulated wealth is considerably higher than that of income among individual sons. The analysis of correlations between the wealth and the income indicators vis-a-vis fathers' and sons' characteristics shows that fathers' labor characteristics, in particular--their occupations, work status, and education--provide significant and coherent patterns for improvement of economic positions of sons. Wealth mobility by places of origin and residence is sensitive to influx of migrants' fathers for India. The analysis of incidences of upward wealth and income mobility by working status and occupations has shown that the results are sensitive to the transition process between fathers and sons in the labor market, from non-wage to wage employment, and from low paying and less skilled jobs to more skilled and better paying ones.^ieng


Subject(s)
Child , Economics , Family Characteristics , Fathers , Nuclear Family , Parents , Social Class , Socioeconomic Factors , Adolescent , Age Factors , Asia , Demography , Developing Countries , Employment , Family Relations , Income , Pakistan , Population , Population Characteristics , Salaries and Fringe Benefits
4.
J Invest Dermatol ; 84(1): 31-2, 1985 Jan.
Article in English | MEDLINE | ID: mdl-3880794

ABSTRACT

Isolated mouse tail skin was UV-irradiated in vitro at a dose of 40 mJ/cm2 from both sides to remove the Ia immunogenicity. Immediately after irradiation the skin was transplanted onto the flank of allogeneic mice. When there was a total H-2 difference between donor and recipient, the UV-irradiated skin did not show a prolonged survival compared to control grafts. In the case of an I-region difference only, i.e., B10.AQR grafts onto B10.T (6R) recipients, a significant prolongation of the survival time was observed, whereas 50% of the UV-treated grafts were not rejected at all.


Subject(s)
Graft Survival/radiation effects , Skin Transplantation , Ultraviolet Rays , Animals , Histocompatibility Antigens/immunology , Histocompatibility Antigens Class II/radiation effects , Mice , Mice, Inbred Strains , Skin/immunology , Skin/radiation effects , Transplantation, Homologous
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