Inefficient internalization of receptor-bound low density lipoprotein in human carcinoma A-431 cells

Human epithelioid carcinoma A-431 cells are known to express unusually large numbers of receptors for the polypeptide hormone epidermal growth factor. The current studies demonstrate that this cell line also expresses 5- to 10-fold more low density lipoprotein (LDL) receptors per cell than either human fibroblasts or Chinese hamster ovary (CHO) cells. As visualized with an LDL-ferritin conjugate, the LDL receptors in A-431 cells appeared in clusters that were distributed uniformly over the cell surface, occurring over flat regions of the membrane as well as over the abundant surface extensions. Only 4% of the LDL receptors were located in coated pits. The LDL receptors in A-431 cells showed the same affinity and specificity as the LDL receptors in human fibroblasts and other cell types. In addition, they were subject to feedback regulation by sterols in the same manner as the LDL receptors in other cells. However, in contrast to other cell types in which the receptor-bound LDL is internalized with high efficiency, in the A-431 cells only a small fraction of the receptor-bound LDL entered the cell. In CHO cells approximately 66% of the LDL receptors were located over coated regions of membrane, and the efficiency of LDL internalization was correspondingly 10-fold higher than in A-431 cells. These findings support the concept that the rate of LDL internalization is proportional to the number of LDL receptors in coated pits and that the inefficiency of internalization in the A-431 cells is caused by a limitation in the ability of these cells to incorporate their LDL receptors into coated pits.

[1]  M. Brown,et al.  Receptor-mediated endocytosis: insights from the lipoprotein receptor system. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[2]  M. Brown,et al.  Inhibition of cholesterol synthesis with compactin renders growth of cultured cells dependent on the low density lipoprotein receptor. , 1979, The Journal of biological chemistry.

[3]  Joseph L. Goldstein,et al.  Coated pits, coated vesicles, and receptor-mediated endocytosis , 1979, Nature.

[4]  L. Orci,et al.  Binding and internalization of 125I-LDL in normal and mutant human fibroblasts. A quantitative autoradiographic study. , 1979, Experimental cell research.

[5]  S. Cohen,et al.  Direct visualization of the binding and internalization of a ferritin conjugate of epidermal growth factor in human carcinoma cells A-431 , 1979, The Journal of cell biology.

[6]  L. Orci,et al.  Epidermal growth factor: morphological demonstration of binding, internalization, and lysosomal association in human fibroblasts. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[7]  S. Singer,et al.  Visualization by fluorescence of the binding and internalization of epidermal growth factor in human carcinoma cells A-431. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[8]  B. Pearse On the structural and functional components of coated vesicles. , 1978, Journal of molecular biology.

[9]  Richard G. W. Anderson,et al.  A mutation that impairs the ability of lipoprotein receptors to localise in coated pits on the cell surface of human fibroblasts , 1977, Nature.

[10]  N. Stone,et al.  Genetics of the LDL receptor: Evidence that the mutations affecting binding and internalization are allelic , 1977, Cell.

[11]  Richard G. W. Anderson,et al.  Role of the coated endocytic vesicle in the uptake of receptor-bound low density lipoprotein in human fibroblasts , 1977, Cell.

[12]  G. Todaro,et al.  Nerve growth factor receptors on human melanoma cells in culture. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[13]  M. Brown,et al.  The low-density lipoprotein pathway and its relation to atherosclerosis. , 1977, Annual review of biochemistry.

[14]  M. Brown,et al.  Localization of low density lipoprotein receptors on plasma membrane of normal human fibroblasts and their absence in cells from a familial hypercholesterolemia homozygote. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[15]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.