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Metabolism of cationized lipoproteins by human fibroblasts: biochemical and morphologic correlations
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Human plasma low density lipoprotein (LDL) that had been rendered polycationic by coupling with N, N-dimethyl-1, 3-propanediamine (DMPA) was shown by electron microscopy to bind in clusters to the surface of human fibroblasts. The clusters resembled those formed by polycationic ferritin (DMPA-feritin), a visual probe that binds to anionic site on the plasma membrane. Biochemical studies with (125)I-labeled DMPA-LDL showed that the membrane-bound lipoprotein was internalized and hydrolyzed in lysosomes. The turnover time for cell bound (125)I-DMPA-LDL, i.e., the time in which the amount of (125)I-DMPA-LDL degraded was equal to the steady-state cellular content of the lipoprotein, was about 50 h. Because the DMPA-LDL gained access to fibroblasts by binding nonspecifically to anionic sites on the cell surface rather than by binding to the physiologic LDL receptor, its uptake failed to be regulated under conditions in which the uptake of native LDL was reduced by feedback suppression of the LDL receptor. As a result, unlike the case with native LDL, the DMPA-LDL accumulated progressively within the cell, and this led to a massive increase in the cellular content of both free and esterified cholesterol. Studies with (14)C-oleate showed that at least 20 percent of the accumulated cholesteryl esters represented cholesterol that had been esterified within the cell. After 4 days of incubation with 10 μg/ml of DMPA-LDL, fibroblasts had accumulated so much cholesteryl ester that neutral lipid droplets were visible at the light microscope level with Oil Red O staining. By electron microscopy, these intracellular lipid droplets were observed to lack a tripartite limiting membrane. The ability to cause the overaccumulation of cholesteryl esters within cells by using DMPA-LDL provides a model system for study of the pathologic consequences at the cellular level of massive deposition of cholesteryl ester. 相似文献
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Itai Doron Irina Leonardi Xin V. Li William D. Fiers Alexa Semon Meghan Bialt-DeCelie Mélanie Migaud Iris H. Gao Woan-Yu Lin Takato Kusakabe Anne Puel Iliyan D. Iliev 《Cell》2021,184(4):1017-1031.e14
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88.
Identification of two quantitative trait loci involved in antibody production on mouse chromosome 8 总被引:1,自引:1,他引:0
A. Puel Jean-Claude Mevel Yolande Bouthillier Claude Decreusefond Wolf H. Fridman Nicole Feingold D. Mouton 《Immunogenetics》1998,47(4):326-331
Several quantitative trait loci (QTLs) contributing to the extreme phenotypes of the selected high (H) and low (L) antibody-responder
lines of mice were mapped on distinct chromosomes. Successive backcrosses were bred to reduce the length of the QTL-bearing
segment detected on chromosome 8 and to produce congenic lines to test gene effect independently of the other QTLs. An increase
in antibody responses was repeatedly found to be associated with inheritance of the H-line allele at two markers separated
by 30 cM on that chromosome. In the successive backcrosses, background and unlinked involved genes of H-line origin were progressively
eliminated; however, unexpected within-progeny variations persisted in the third and even fourth backcross. Nevertheless,
the presence of two QTLs within the considered interval was definitely demonstrated in distinct progenies of the fourth backcross
which separately inherited one of the two gene-marker H-line alleles. The previously identified chromosome 8 segment therefore
contains at least two QTLs involved in antibody responsiveness.
Received: 19 August 1997 / Revised: 9 October 1997 相似文献
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