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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 121 (1993), S. 31-36 
    ISSN: 1573-4919
    Keywords: aging ; cholinephosphotransferase ; mitochondria ; microsomes ; lung ; guinea pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract It is known that the composition of phospholipids in lung changes with age. The final step in thede novo synthesis of phosphatidylcholine, a major component of lung surfactant, by the CDP-choline pathway, requires the enzyme cholinephosphotransferase (CPT). Even though CPT has earlier been proposed to be located exclusively in the endoplasmic reticulum, we have recently demonstrated its presence also in the mitochondria. We have earlier reported a gestational variation of CPT activity in fetal mitochondria and microsomes. In the present study we examined the subcellular distribution of CPT activity in lung as a function of age. After birth, the microsomal CPT activity continued to increase until adulthood (24 wks of age), thereafter it gradually decreased. On the otherhand, the CPT activity of mitochondria continued to increase with the advancement of age and beyond 72 wks of age, it was approximately 2-fold higher than that of the microsomal fraction.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-4919
    Keywords: calcium-dependent phospholipid-binding proteins (annexins) ; lung ; alveolar type II cells ; lavage fluid ; guinea pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract A new group of calcium-regulating proteins, called annexins or Ca++-dependent phospholipid-binding proteins (PLBP), have been detected in different species, organs and cell types. In the present study, we have identified and quantitated PLBP from guinea pig lung, lavage fluid and alveolar type II cells to elucidate the possible role of PLBP in lung surfactant biogenesis and secretion. Lungs were lavaged and type II cells from lavaged lung were isolated by elastase digestion and purified by centrifugal elutriation. For the quantitative identification of PLBP, we performed ELISA assays and Western blot analysis by using an antiserum raised in guinea pigs against a pure rabbit lung 36 kDa PLBP. The lavage fluid, cytosol from lung and type II cells contained 784,167 and 435 ng per mg protein, respectively, of PLBP. The SDS-PAGE electrophoretic pattern and Western blot confirmed that all lung samples have band corresponding to a 36 kDa protein. This indicates that both alveolar type II cells and lavage fluid have higher levels of PLBP than whole lung cytosol.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 140 (1994), S. 49-54 
    ISSN: 1573-4919
    Keywords: capillary endothelial cells ; β-adrenoreceptor ; cell proliferation ; endothelial cell culture ; angiogenesis ; adenylate cyclase-cAMP system
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract β-Adrenoreceptor has been studied in a clonal capillary endothelial cell line established from the vascular bed of the bovine adrenal medulla. [3H]Dihydroalprenolol ([3H]DHA) binding to the isolated plasma membranes from these cells has demonstrated the presence of β-adrenoreceptors with two different affinities. the dissociation constants (Kd) have been found to be 0.27±0.09×10−9 M and 2.96±0.31×10−9 M, respectively with the corresponding Bmax of 5.1±0.05 and 70.0±0.2 pmol/mg protein, respectively. Inhibition of [3H]DHA binding to the β-receptor by atenolol (a β1-antagonist) and ICI 118,551 (a β1-antagonist) has suggested that the IC50cor (=Ki) for atenolol and ICI 118,551 for high affinity site are 0.08±0.03×10−12 M and 0.25±0.08×10−12 M, respectively. This, therefore, indicates that both atenolol and ICI 118,551 are able to displace the bound ligand effectively but the β1-selective antagonist atenolol is 3 times more potent than its β2 counterpart, ICI 118,551. Displacement of [3H]DHA binding to the endothelial cell plasma membrane by the agonists isoproterenol, epinephrine and norephinephrine has established a relative order of Ki for these agents as isoproterenol (0.56±0.19×10−9 M)〈epinephrine (0.77±0.26−9 M)〉-norepinephrine (0.71±0.24×10−9 M) for the high affinity site. The corresponding values for the low affinity site, however, are 4.62±0.64×10−9 M, 6.21±0.86×10−9 M and 5.90±0.82×10−9 M, respectively for the same agonists. Increased intracellular cAMP accompanied with cellular proliferation in the presence of isoproterenol has suggested not only the coupling of β-adrenoreceptors to the adenylate cyclase system but also its involvement in endothelial cell proliferation.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4919
    Keywords: cholinephosphotransferase ; mitochondria ; microsomes ; fetal lung ; guinea pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Summary We have reported earlier that cholinephosphotransferase (EC 2.7.8.2) is present in both mitochondria and microsomes of fetal guinea pig lung. This study was designed to compare the properties of mitochondrial and microsomal cholinephosphotransferase in fetal guinea pig lung. Various parameters, such as substrate specificity, Km values, sensitivity to N-ethylmaleimide, dithiothreitol and trypsin were measured. Both showed significant preference for unsaturated diacylglycerols over saturated diacylglycerols. Data on Km and Vmax indicate that the affinity of this enzyme for different diacylglycerols varies between the two forms. The ID50 values for N-ethylmaleimide were 20 mM and 12.5 mM for the mitochondrial and microsomal form of the enzyme, respectively. Dithiothreitol showed an inhibitory effect on both; however, the mitochondrial form was inhibited less than the microsomal form. The effects of N-ethylmaleimide and dithiothreitol on both forms of enzyme indicated that the microsomal cholinephosphotransferase requires a higher concentration of -SH for its activity than the mitochondrial enzyme does. The enzyme was inhibited by trypsin in both mitochondria and microsome under isotonic condition suggesting that this enzyme is on the outside of the membrane in both endoplasmic reticulum and mitochondria.
    Type of Medium: Electronic Resource
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