Clathrin-dependent Receptor-mediated Endocytosis Research Articles

Papillomaviruses infect cells via a clathrin-dependent pathway

In this study we have examined the pathway by which papillomaviruses infect cells, using bovine papillomavirus (BPV) virions and mouse C127 cells as the model system. By confocal microscopy, the entry of BPV virions, BPV virus-like particles (VLPs), and HPV16 VLPs were very similar. In dually exposed cells, HPV-16 VLPs and BPV virions colocalized intracellularly. BPV VLPs colocalized with AP-2, a clathrin adapter molecular and a marker of the clathrin-dependent endocytic pathway; and also with transferrin receptor, a marker of early endosomes; and Lamp-2, a marker of late endosomes and lysosomes. BPV infection was detected within 12 h of virion cell-surface binding, as measured by an RT-PCR assay. Infection was prevented by several pharmacologic inhibitors, including chlorpromazine, which blocks clathrin-dependent endocytosis and the lysosomotropic agent, bafilomycin A. By contrast, two inhibitors of caveolae-dependent uptake, filipin and nystatin, did not prevent BPV infection. We conclude that papillomaviruses infect cells via clathrin-dependent receptor-mediated endocytosis. Surprisingly, the kinetics of internalization were unusually slow for this mechanism, with the t 1/2 of entry of BPV-1 being approximately 4 h versus 5–15 min for a typical ligand.

The route of bacterial uptake by macrophages influences the repertoire of epitopes presented to CD4 T cells.

We studied MHC class II (MHC-II)-restricted antigen processing of viable Streptococcus pyogenes by murine macrophages for presentation of two CD4 T cell epitopes of the surface M5 protein. We show that presentation of both epitopes was prevented if actin polymerization was inhibited by cytochalasin D, but not if clathrin-dependent receptor-mediated endocytosis was prevented, suggesting uptake of streptococci by phagocytosis or macropinocytosis was required for presentation of the surface M protein. However, treatment of macrophages with amiloride, which selectively blocks membrane ruffling and subsequent macropinocytosis, inhibited the response to one epitope (M5(308-319)), but had no effect on presentation of the other (M5(17-31)). The effect of the inhibitors on uptake of streptococci was analyzed by electron microscopy. Cytochalasin D completely blocked uptake of streptococci, while dimethyl-amiloride only inhibited uptake into spacious compartments. Neither of the inhibitors altered the cell-surface expression of MHC-II and costimulatory molecules analyzed by flow cytometry. The data suggest that distinct epitopes of a protein associated with viable bacteria may be presented optimally following different uptake mechanisms in the same antigen-presenting cells.

NHE3 serves as a molecular tool for cAMP-mediated regulation of receptor-mediated endocytosis.

Receptor-mediated, clathrin-dependent endocytosis (RME) is important for macromolecular transport and regulation of cell-surface protein expression. Pharmacological studies have shown that the plasma membrane transport protein Na(+)/H(+) exchanger 3 (NHE3), which shuttles between the plasma membrane and the early endosomal compartment by means of clathrin-mediated endocytosis, contributes to endosomal pH homeostasis and endocytic fusion events. Furthermore, it is known that NHE3 is phosphorylated and inhibited by cAMP-dependent kinase (protein kinase A). Here, we show, in a cellular knockout/retransfection approach, that NHE3 supports RME and confers cAMP sensitivity to RME, using megalin/cubilin-mediated albumin uptake in opossum kidney cells. RME, but not fluid-phase endocytosis, was dependent on NHE3 activity and expression. Furthermore, NHE3 deficiency or inhibition reduced the relative surface expression of megalin without altering total expression. In wild-type cells, cAMP inhibits NHE3 activity, leads to endosomal alkalinization, and reduces RME. In NHE3-deficient cells, endosomal pH is not sensitive to NHE3 inhibition, and cAMP does not affect endosomal pH or RME. NHE3 transfection into deficient cells restores RME and the effects of cAMP. Thus our data show that NHE3 is important for cAMP sensitivity of clathrin-dependent RME.

Functional recovery of senescent cells through restoration of receptor-mediated endocytosis

The functional deterioration of an organism with age causes the major problem of maintaining the quality of life at old age. Degenerative changes in the organism may to some extent reflect alterations that can be observed in cells during in vitro replicative senescence. At the cellular level, the receptor-mediated endocytosis in the membrane might be emphasized as a responsible mechanism for functional decay, since the endocytosis is in charge of many important biological phenomena: nutrient uptake, growth factor sensitivity, immune response, protection from environment and pathogen uptake, etc. We found that two major endocytotic pathways, i.e. clathrin-mediated and caveolae-dependent endocytosis, are down regulated in senescent cells. For the down regulation of the clathrin dependent receptor-mediated endocytosis, the reduction of amphiphysin-1 was found responsible, which was confirmed by Western blot analysis, dominant negative mutant transfection and restoration of gene activity by microinjection. With respect to the hypo-responsiveness of senescent cells to growth factors, the upregulation of caveolins has been suggested to be a causal factor. The overexpression of caveolins caused senescent-like changes in epidermal growth factor (EGF) response of the young cells, while down regulation of caveolins by use of antisense-oligonucleotides restored the EGF response in old cells, suggesting that caveolin system would be one of the major mechanisms responsible for decreased responses to growth factors in the senescent cells. Based on these results, it can be suggested that the functional deterioration of the senescent cells may be explained in terms of the down regulation of receptor mediated endocytosis, at least in part, and that the restoration of endocytosis apparatus either with amphiphysin supplementation or with reduction of caveolins might lead to functional recovery of the senescent cells.

Down-regulation of receptor-mediated endocytosis is responsible for senescence-associated hyporesponsiveness.

Human diploid fibroblasts (HDF) do not divide indefinitely and eventually lead to an arrest of cell division by a process termed cellular or replicative senescence. Irreversible growth arrest of senescent cells is strongly related to the attenuated response to growth factors. Recently, we reported that up-regulation of caveolin in the senescent cells is responsible for the attenuated response to growth factors. Senescent cells did not phosphorylate Erk-1/2 after EGF stimulation, whereas young cells did. In those senescent cells, we found an increased level of caveolin proteins and strong interactions between caveolin-1 and EGFR. When we overexpressed caveolin-1 in young HDF, the activation of Erk-1/2 on EGF stimulation was significantly suppressed. These results suggest that the hyporesponsiveness of senescent fibroblasts to EGF stimulation might be due to the overexpression of caveolin. In addition, the clathrin-dependent endocytosis system plays the more active and dominant role over the caveolae system. Therefore, we monitored the efficiency of clathrin-dependent receptor-mediated endocytosis in the senescent cells in order to elucidate the exact mode of the attenuated response to growth factors in the senescent cells. Using a transferrin-uptake assay and Western blot analysis of endocytosis-related proteins, we found a significant decrease of amphiphysin-1 in human diploid fibroblasts of multipassages. By adjusting the level of amphiphysin, we could modulate the efficiency of receptor-mediated endocytosis either in young or old cells toward growth factors: that is, a dominant negative mutant of amphiphysin-1 blocked the endocytosis in the young cells, while microinjection of the gene resumed its activity in the old cells. Taken together, we conclude that the loss of endocytotic activity of senescent cells is directly related to the down-regulation of amphiphysin-1 and/or up-regulation of caveolins. This opens a new field of functional recovery of the senescent cells simply through adjusting the receptor-mediated endocytosis capacity.

Down‐regulation of amphiphysin‐1 is responsible for reduced receptor‐mediated endocytosis in the senescent cells

See CORRECTIONSPECIFIC AIMSHuman diploid fibroblasts undergo multiple functional alterations during their senescence process. Most of all, senescent cells do not respond properly to external stimuli and do not uptake materials as efficiently as presenescent cells. To elucidate the reason for such attenuated response of senescent cells, we attempted to monitor the functional capacity and molecular mechanism for the clathrin-dependent, receptor-mediated endocytosis in the senescent cells, and tried to find principal molecules responsible for the decreased endocytotic activity in senescent cells that might be a target of intervention for the age-related dysfunctions.PRINCIPAL FINDINGS1. Clathrin-dependent receptor-mediated endocytosis is blocked in senescent human diploid fibroblastsTo investigate the functional changes in the receptor-mediated endocytosis during cellular senescence, we treated the early and late-passaged fibroblasts with tetramethylrhodamine-conjugated transferrin. Presenescent fibroblasts ...

Mechanisms ofStaphylococcus aureusinvasion of cultured osteoblasts

Staphylococcus aureusis a bacterial pathogen causing approximately 80% of all cases of human osteomyelitis. This bacterium can adhere to and become internalized by osteoblasts and previous studies indicate that osteoblasts are active in the internalization process. In the current study, we examined the roles of microfilaments, microtubules and clathrin-dependent receptor-mediated endocytosis in the internalization ofS. aureusby MC3T3-E1 mouse osteoblast cells. Microfilament and microtubule polymerization was inhibited with cytochalasin D and colchicine. Clathrin-coated pit formation was examined by using the transaminase inhibitor, monodanslycadaverine. The results of this study indicate that mouse osteoblasts utilize actin microfilaments, microtubules and clathrin-coated pits in the internalization ofS. aureus; however, microfilaments seem to play the most significant role in the invasion process.

The clathrin endocytic pathway in viral infection.

How important is the clathrin-dependent endocytic pathway for entry of viruses into host cells? While it is widely accepted that Semliki Forest virus (SFV), an enveloped virus, requires this pathway there are conflicting data concerning the closely related Sindbis virus, as well as varying results with picornaviruses such as human rhinovirus 14 (HRV 14) and poliovirus. We have examined the entry mode of SFV, Sindbis virus, HRV 14 and poliovirus using a method that identifies single infected cells. This assay takes advantage of the observation that the clathrin-dependent endocytic pathway is specifically and potently arrested by overexpression of dynamin mutants that prevent clathrin-coated pit budding. Using HeLa cells and conditions of low multiplicity of infection to favor use of the most avid pathway of cell entry, it was found that SFV, Sindbis virus and HRV 14 require an active clathrin-dependent endocytic pathway for successful infection. In marked contrast, infection of HeLa cells by poliovirus did not appear to require the clathrin pathway.