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• W2023179617 abstract "Senescent human diploid fibroblasts do not respond to growth factors like epidermal growth factor (EGF), although they have a normal level of receptors and downstream signaling molecules. To examine the mechanism of signaling attenuation, we investigated Erk activation after EGF stimulation in senescent cells. 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 EGF receptor. Electron microscopic analysis demonstrated an increased number of caveolae structures in senescent cells. More interestingly, brain, spleen, and lung from 26-month-old rats showed substantial increases of caveolin proteins. However, in the case of p53-induced senescence, caveolin-1 was not induced, and EGF stimulation phosphorylated Erk-1/2 as much as young control cells. Finally, we overexpressed caveolin-1 in young human diploid fibroblasts in which the activation of Erk-1/2 upon EGF stimulation was significantly suppressed. These results suggest that the unresponsiveness of senescent fibroblasts to EGF stimulation may be due to the overexpression of caveolins, which seems to be independent of growth arrest and other aging phenotypes. Senescent human diploid fibroblasts do not respond to growth factors like epidermal growth factor (EGF), although they have a normal level of receptors and downstream signaling molecules. To examine the mechanism of signaling attenuation, we investigated Erk activation after EGF stimulation in senescent cells. 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 EGF receptor. Electron microscopic analysis demonstrated an increased number of caveolae structures in senescent cells. More interestingly, brain, spleen, and lung from 26-month-old rats showed substantial increases of caveolin proteins. However, in the case of p53-induced senescence, caveolin-1 was not induced, and EGF stimulation phosphorylated Erk-1/2 as much as young control cells. Finally, we overexpressed caveolin-1 in young human diploid fibroblasts in which the activation of Erk-1/2 upon EGF stimulation was significantly suppressed. These results suggest that the unresponsiveness of senescent fibroblasts to EGF stimulation may be due to the overexpression of caveolins, which seems to be independent of growth arrest and other aging phenotypes. epidermal growth factor EGF receptor mitogen-activated protein kinase/extracellular signal-regulated kinase kinase population doubling level human diploid fibroblast extracellular signal-regulated kinase Normal human diploid cells show cellular senescence in vitro after a finite number of population doublings (1.Hayflick L. Moorehead P.S. Exp. Cell Res. 1961; 25: 585-621Crossref PubMed Scopus (5300) Google Scholar). Although senescent cells can maintain their metabolic activity, the loss of proliferation capacity may be due to a diminished response to growth factors (2.Matsuda T. Okamura K. Sato Y. Morimoto A. Ono M. Kohno K. Kuwano M. J. Cell. Physiol. 1992; 150: 510-516Crossref PubMed Scopus (51) Google Scholar, 3.Seshadri T. Campisi J. Science. 1990; 247: 205-209Crossref PubMed Scopus (420) Google Scholar, 4.Riabowol K. Schiff J. Gilman M.Z. Proc. Natl. Acad. Sci. U. S. A. 1992; 89: 157-161Crossref PubMed Scopus (181) Google Scholar). In aged human diploid fibroblasts, the decreased response to growth factors is suggested to be associated with a repression of c-fos expression, a reduced AP-1 DNA binding, and diminished DNA synthesis. Senescent cells in culture or tissues have been reported to have normal numbers of EGF1 receptors (EGFRs) (5.Hensler P.J. Pereira-Smith O.M. Am. J. Pathol. 1995; 147: 1-8PubMed Google Scholar,6.Ribault D. Habib M. Abdel-Majid K. Barbara A. Mitrovic D. Mech. Ageing Dev. 1998; 100: 25-40Crossref PubMed Scopus (33) Google Scholar), and the binding capacity of EGF to EGFR is normal (7.Peacocke M. Campisi J. J. Cell. Biochem. 1991; 45: 147-155Crossref PubMed Scopus (66) Google Scholar). However, there is no mitogen-activated protein kinase activation upon EGF stimulation in senescent cells, and the mechanism for the age-related modulation of EGFR in response to the EGF stimulation is not yet fully resolved. Caveolae are vesicular invaginations of the plasma membrane with a diameter of 50–100 nm (8.Severs N.J. J. Cell Sci. 1988; 90: 341-348Crossref PubMed Google Scholar, 9.Anderson R.G. Proc. Natl. Acad. Sci. U. S. A. 1993; 90: 10909-10913Crossref PubMed Scopus (565) Google Scholar) and regulate signal transduction, potocytosis, and transcytosis (10.Engelman J.A. Chu C. Lin A. Jo H. Ikezu T. Okamoto T. Kohtz D.S. Lisanti M.P. FEBS Lett. 1998; 428: 205-211Crossref PubMed Scopus (346) Google Scholar, 11.Lisanti M.P. Scherer P.E. Vidugiriene J. Tang Z. Hermanowski-Vosatka A. Tu Y.H. Cook R.F. Sargiacomo M. J. Cell Biol. 1994; 126: 111-126Crossref PubMed Scopus (806) Google Scholar). Caveolin, a 21–24-kDa integral membrane protein, is a principal structural component of caveolae membranes in vivo. The stable expression of the caveolin-1 or -3 gene to the mammalian cells without caveolin induced the formation of caveolae structures (12.Lipardi C. Mora R. Colomer V. Paladino S. Nitsch L. Rodriguez-Boulan E. Zurzolo C. J. Cell Biol. 1998; 140: 617-626Crossref PubMed Scopus (131) Google Scholar). Caveolin functions as a scaffolding protein within the caveolae membrane and interacts with signaling proteins, namely EGFR, G-proteins, Src-like kinases, Ha-Ras, protein kinase C, endothelial nitric-oxide synthase, integrin and so on (13.Li S. Couet J. Lisanti M.P. J. Biol. Chem. 1996; 271: 29182-29190Abstract Full Text Full Text PDF PubMed Scopus (667) Google Scholar, 14.Ko Y.-G. Lee J.-S. Kang Y.-S. Ahn J.-H. Seo J.-S. J. Immunol. 1999; 162: 7217-7223PubMed Google Scholar, 15.Ko Y.-G. Liu P. Pathak R.K. Craig L.C. Anderson R.G. J. Cell. Biochem. 1998; 71: 524-535Crossref PubMed Scopus (36) Google Scholar, 16.Garcia-Cardena G. Martasek P. Masters B.S. Skidd P.M. Couet J. Li S. Lisanti M.P. Sessa W.C. J. Biol. Chem. 1997; 272: 25437-25440Abstract Full Text Full Text PDF PubMed Scopus (689) Google Scholar, 17.Couet J. Sargiacomo M. Lisanti M.P. J. Biol. Chem. 1997; 272: 30429-30438Abstract Full Text Full Text PDF PubMed Scopus (538) Google Scholar, 18.Okamoto T. Schlegel A. Scherer P.E. Lisanti M.P. J. Biol. Chem. 1998; 273: 5419-5422Abstract Full Text Full Text PDF PubMed Scopus (1336) Google Scholar). A short cytosolic N-terminal region of caveolin is involved in the formation of oligomers and mediates the interaction with these signal molecules, which results in the inactivation of signaling (11.Lisanti M.P. Scherer P.E. Vidugiriene J. Tang Z. Hermanowski-Vosatka A. Tu Y.H. Cook R.F. Sargiacomo M. J. Cell Biol. 1994; 126: 111-126Crossref PubMed Scopus (806) Google Scholar). The suppression of these signaling molecules can be circumvented by a tumor, wherein caveolins are generally down-regulated. Targeted down-regulation of caveolin-1 is sufficient to drive cell transformation and hyperactivates the Erk kinase cascade (19.Galbiati F. Volonte D. Engelman J.A. Watanabe G. Burk R. Pestell R.G. Lisanti M.P. EMBO J. 1998; 17: 6633-6648Crossref PubMed Scopus (428) Google Scholar). Co-expression with caveolin-1 dramatically inhibits signaling from EGFR, Raf, MEK-1, and Erk-2 to the nucleus in vivo (10.Engelman J.A. Chu C. Lin A. Jo H. Ikezu T. Okamoto T. Kohtz D.S. Lisanti M.P. FEBS Lett. 1998; 428: 205-211Crossref PubMed Scopus (346) Google Scholar). In order to find an explanation for the attenuated responsiveness to EGF stimulation in senescent cells, we examined the signaling pathways of Erk activation after EGF stimulation. Interestingly, these differences in signaling behavior were consistent with the expression of caveolins in aged cells. Moreover, p53-mediated senescent cells respond differently to EGF stimulation, although they showed the same senescence-associated β-galactosidase activity and delayed doubling time. EJ-p53 cells did not express caveolin-1 proteins and did not show the attenuated EGF response despite the phenotypic cellular senescent changes. To know the direct effect of caveolin in HDFs, we overexpressed caveolin-1 in young HDFs. The phosphorylation of Erk-1/2 upon EGF stimulation was significantly blocked by caveolin-1 expression in young HDFs. Our results suggest that the expression of caveolin and the resulting formation of caveolae might be responsible for the attenuation of EGF signaling in senescent cells. Human diploid fibroblasts were isolated from newborn foreskin (20.Park S.C. Yeo E.-J. Han J.-A. Hwang Y.-C. Choi J.-Y. Park J.S. Park Y.-H. Kim K.-O. Kim I.-G. Seong S.-C. Kwak S.-J. J. Gerontol. 1999; 54: B78-B83Crossref Scopus (25) Google Scholar), and IMR-90 was purchased from ATCC (CCL-186). EJ-p53 cells were obtained from Dr. D. Y. Shin (21.Sugrue M.M. Shin D.Y. Lee S.W. Aaronson S.A. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 9648-9653Crossref PubMed Scopus (258) Google Scholar), and Harlan Sprague-Dawley rats were purchased and maintained from the Animal Laboratory of Seoul National University College of Medicine. Monoclonal anti-caveolin-1 antibody (C43420), monoclonal anti-caveolin-2 antibody (C57820), and monoclonal anti-caveolin-3 antibody (C38320) were purchased from Transduction Laboratories. Polyclonal anti-EGFR antibody (sc-03), polyclonal anti-phospho-Erk antibody (sc-7383), polyclonal anti-Erk-1/2 antibody (sc-94), anti-p53 antibody (sc-126), and anti-p21 antibody (sc-6246) were obtained from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA). Secondary horseradish peroxidase-conjugated anti-rabbit or anti-mouse antibodies were purchased from Jackson Immunochemicals. Other biochemical reagents were purchased from Sigma and Life Technologies, Inc. Human diploid fibroblasts and IMR-90 were kept in 10-cm plates in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum and antibiotics and subcultured at a 1:4 ratio. Young cells are defined as resulting from less than 25 population doublings, whereas old cells were from more than 60 population doublings. The senescence of all old cells was confirmed by their delayed population doubling times and by senescence-associated β-galactosidase activity assay as described by Dimri et al. (22.Dimri G.P. Lee X. Basile G. Acosta M. Scott G. Roskelley C. Medrano E.E. Linskens M. Rubelj I. Pereira-Smith O. Peacocke M. Campisi J. Proc. Natl. Acad. Sci. U. S. A. 1995; 92: 9363-9367Crossref PubMed Scopus (5558) Google Scholar). EJ-p53 cells were maintained as described by Sugrue et al. (21.Sugrue M.M. Shin D.Y. Lee S.W. Aaronson S.A. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 9648-9653Crossref PubMed Scopus (258) Google Scholar). Harlan Sprague-Dawley rats were maintained on a normal diet for more than 24 months; tumor-free female rats were used for this experiment. 8–10-week-old female rats were used as young controls. After being grown in a semiconfluent state, senescence-associated β-galactosidase (pH 6.0) activity was examined (22.Dimri G.P. Lee X. Basile G. Acosta M. Scott G. Roskelley C. Medrano E.E. Linskens M. Rubelj I. Pereira-Smith O. Peacocke M. Campisi J. Proc. Natl. Acad. Sci. U. S. A. 1995; 92: 9363-9367Crossref PubMed Scopus (5558) Google Scholar). Briefly, cells were washed with phosphate-buffered saline and fixed with 2% paraformaldehyde, 0.2% glutaraldehyde in phosphate-buffered saline for 5 min at room temperature. After washing with phosphate-buffered saline, cells were incubated with β-galactosidase reagent (1 mg/ml X-gal, 40 mm citric acid/sodium phosphate buffer, pH 6.0, 5 mm potassium ferrocyanide/potassium ferricyanide, 150 mm NaCl, 2 mm MgCl2) at 37 °C. Total cell or tissue lysates were extracted using extraction buffer (10 mm Tris-HCl, pH 7.5, 1 mm EDTA, 150 mm NaCl, 1% Triton X-100, 1 mmphenylmethylsulfonyl fluoride, 2 μg/ml aprotinin, 2 μg/ml leupeptin, 50 mm NaF, 0.2 mmNa3VO4) and sonicated briefly. Lysates were separated using SDS-polyacrylamide gel electrophoresis and transferred onto nitrocellulose filters (Protran; Schleicher & Schuell) using standard techniques. After immunoblotting the membrane with a primary antibody, the immune complex was incubated with a peroxidase-conjugated anti-mouse or anti-rabbit secondary antibody and finally visualized using an enhanced chemiluminescence detection kit (ECL kit; Amersham Pharmacia Biotech). Cells were lysed in IP lysis buffer (10 mm phosphate buffer, pH 7.4, 150 mm NaCl, 1% Nonidet P-40, 2 mm EDTA, 1 mmphenylmethylsulfonyl fluoride, 2 μg/ml aprotinin, 2 μg/ml leupeptin, 50 mm NaF, 0.2 mmNa3VO4) and sonicated briefly. Lysates were spin down at 9,000 rpm for 5 min, and supernatants were incubated with normal mouse serum, anti-EGFR antibody, and anti-caveolin-1 antibody. Immune complexes were precipitated with protein A-Sepharose beads (Amersham Pharmacia Biotech) and separated by SDS-polyacrylamide gel electrophosresis and Western blot. Subconfluent cells at early and late PDLs were pelletized and fixed with 3% glutaraldehyde/phosphate-buffered saline at pH 7.4. After washing with 0.2 m sodium cacodylate buffer, pH 7.4, cell pellets were treated with 1% osmium tetroxide in cacodylate buffer for 1 h. The cells were then dehydrated in graded ethanol steps through propylene oxide and embedded in epoxy resin (Polyscience Co.). Ultrathin sections were cut and stained with uranyl acetate and lead citrate. Sections were observed using a transmission electron microscope (H-600, Hitachi). Using total cell extracts, total cholesterol levels were measured using the cholesterol oxidase method (Roche Molecular Biochemicals). The mean value of the cholesterol level and S.E. values were calculated from three independent experiments. Caveolin-1 cDNA was cloned by reverse transcriptase-polymerase chain reaction from old HDF and verified by sequencing. In pcDNA3.1 plasmid DNA (Invitrogen), we subcloned the mammalian expression vector for caveolin-1. Next, we introduced expression vector into young HDF using the liposome-mediated transfection method as described by the manufacturer (LipofectAMINE plus, Life Technologies, Inc.). After 48 h, transfected cells were stimulated with EGF, and the phosphorylation of Erk-1/2 was checked by Western blot. Senescent cells like old rat hepatocytes or old human diploid fibroblasts have been demonstrated to show an age-dependent decline in DNA synthesis and/or cell division upon growth factor stimulation. To explore the mechanism of the reduced response to EGF stimulation with aging, we first examined the phosphorylation and activation of Erk kinases in old cells. Two kinds of primary human fibroblasts were used: primary HDFs isolated from newborn foreskin (20.Park S.C. Yeo E.-J. Han J.-A. Hwang Y.-C. Choi J.-Y. Park J.S. Park Y.-H. Kim K.-O. Kim I.-G. Seong S.-C. Kwak S.-J. J. Gerontol. 1999; 54: B78-B83Crossref Scopus (25) Google Scholar) and IMR-90, human lung fibroblast from ATCC. These cells were kept as described previously (23.Chen Q.M. Bartholomew J.C. Campisi J. Acosta M. Reagan J.D. Ames B.N. Biochem. J. 1998; 332: 43-50Crossref PubMed Scopus (351) Google Scholar) and classified as young (PDL less than 30), middle-aged (PDL 35–45), and old (PDL more than 60) cells. Each group of HDFs was stimulated with EGF, and the activation of Erk-1/2 was determined by Western blot. In both the young and middle-aged cells, Erk-1/2 kinases were phosphorylated within 5 min, and the resulting activation was sustained for 15 min after EGF stimulation (Fig. 1 A). However, the phosphorylation of Erk-1/2 from old HDF was not detected until 15 min had lapsed. Although previous reports have shown the expression of EGFR or downstream signaling molecules in old cells (2.Matsuda T. Okamura K. Sato Y. Morimoto A. Ono M. Kohno K. Kuwano M. J. Cell. Physiol. 1992; 150: 510-516Crossref PubMed Scopus (51) Google Scholar,24.Kitano S. Bohr V.A. Reed T.D. Haggerty C.M. May A. Roth G.S. J. Cell. Physiol. 1998; 176: 32-39Crossref PubMed Scopus (6) Google Scholar), a comparison is needed of the age-dependent level of signaling proteins like Erk kinases and EGFR. The expression level of Erk kinases and EGFR was not changed by the increase of population doubling in Western blot (Fig. 1 B), despite the down-regulation of EGF signaling to Erk kinases. Therefore, the reduced responsiveness of old cells may not be due to the altered protein turnover and post-translational modification, since old HDF cells expressed a comparable amount of EGFR and Erk kinases. These results suggested that there would be a specific modulation mechanism for the signal attenuation and reduced proliferation of old cells upon EGF stimulation. Caveolae have been reported to regulate EGF signaling through direct interactions with EGFR. First we examined whether the expression level of caveolin-1 was increased upon aging HDF (Fig.2 A). With aging, a 22–24-kDa caveolin-1 protein was expressed increasingly in both HDF and IMR-90. Next we tried to examine whether the EGFR from old HDF could interact with caveolin-1, which might suppress EGF signaling through direct molecular interaction as described previously (17.Couet J. Sargiacomo M. Lisanti M.P. J. Biol. Chem. 1997; 272: 30429-30438Abstract Full Text Full Text PDF PubMed Scopus (538) Google Scholar). Lysates from young and old HDF were precipitated with normal mouse sera, anti-caveolin-1 antibody, or anti-EGFR antibody. Then each immune complex was separated by SDS-polyacrylamide gel electrophoresis and analyzed by Western blot using anti-caveolin-1 antibody or anti-EGFR antibody. The immune complex of EGFR from old HDF contained caveolin-1 proteins, while young fibroblasts did not show a comparable amount of caveolin-1 and subsequent interactions with EGFR (Fig. 2 B). Although we did not check the kinase activity of EGFR in old HDF, molecular interaction between caveolin and EGFR may mediate the attenuation of EGF signaling in old HDF. Caveolin-2, a homolog of caveolin-1 (25.Scherer P.E. Okamoto T. Chun M. Nishimoto I. Lodish H.F. Lisanti M.P. Proc. Natl. Acad. Sci. U. S. A. 1996; 93: 131-135Crossref PubMed Scopus (486) Google Scholar), is expressed ubiquitously in most cell types, supposedly forming a hetero-oligomer in basolaterally localized caveolae (26.Scheiffele P. Verkade P. Fra A.M. Virta H. Simons K. Ikonen E. J. Cell Biol. 1998; 140: 795-806Crossref PubMed Scopus (261) Google Scholar). Although the overexpression of caveolin-2 was not sufficient to form functional caveolae structures (27.Li S. Galbiati F. Volonté D. Sargiacomo M. Engelman J.A. Das K. Scherer P.E. Lisanti M.P. FEBS Lett. 1998; 434: 127-134Crossref PubMed Scopus (112) Google Scholar), it would be important to know whether the up-regulation of caveolin-1 is accompanied by an overexpression of caveolin-2. Fig. 2 Ashows that the expression of caveolin-2 in both HDF and IMR-90 was increased with aging, like caveolin-1. The role of caveolin-2 is not well defined, but we suggest that caveolin-2 might potentiate caveolae formation in aged cells. Although the expression of caveolin-3 is restricted to striated muscle cells (28.Tang Z. Scherer P.E. Okamoto T. Song K. Chu C. Kohtz D.S. Nishimoto I. Lodish H.F. Lisanti M.P. J. Biol. Chem. 1996; 271: 2255-2261Abstract Full Text Full Text PDF PubMed Scopus (602) Google Scholar), heterologous expression of caveolin-3 in old human fibroblasts was detected in both HDF and IMR-90 (Fig. 2 A). Caveolin-1, a key constituent of caveolae structures, forms caveolae structures in old HDF. Electron microscopic experiments of plasmalemmal profiles from old (PDL 55–65) HDF revealed the presence of numerous non-clathrin-coated vesicular structures, 50–100 nm in diameter, that are juxtaposed to the plasma membrane and are morphologically indistinguishable from caveolae (Fig.3 A). In contrast, profiles of young (PDL 20–25) cells contained significantly less caveolae-like structure. Quantitative analysis of multiple plasmalemmal profile revealed that old fibroblasts contained over 10 times more caveolae-like structure than young cells (0.5/μm versus5.2/μm, respectively) (Fig. 3 B). Extrapolation of in vitro changes of old cells to in vivo old rat tissues will confer a biological significance in aging research. Every old tissue consists of heterogeneous cell types, especially in the case of proliferation potential. However, the overall function and responsiveness of each organ was significantly down-regulated with aging. To compare the expression of caveolin proteins in each organ, young 2-month-old and old 27-month-old Harlan Sprague-Dawley rats were sacrificed, and the solid organs were dissected out for Western blot analysis. In Fig. 4, all of the major organs showed markedly increased level of caveolin-1 proteins. Aged brain, kidney, lung, and spleen in particular expressed significant quantities of caveolin-1 proteins as well as caveolin-2 and caveolin-3. Moreover, some tissues such as brain, thymus, and spleen showed that the expression of caveolins was highly increased in the old tissues, which is in contrast to their undetectable levels of expression of the young tissues. From these results, the up-regulation of caveolin proteins was consistently found in vivo in old tissues, implicating the role of caveolins in various aging-related phenomena. Senescence-like growth arrest by expression of p53 in EJ human bladder carcinoma cells induced cellular senescence (21.Sugrue M.M. Shin D.Y. Lee S.W. Aaronson S.A. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 9648-9653Crossref PubMed Scopus (258) Google Scholar). To find the causal relationship between caveolin and signaling in old cells, we used EJ-p53 cells as an induced aging model. EJ-p53 cells were induced for senescence by removal of tetracycline from the culture media for more than 7 days. p53 and p21 were induced in p53-induced EJ human bladder carcinoma cells (Fig. 5 A). Senescence-associated β-galactosidase activity was also increased in p53-induced EJ cells (data not shown). However, the responses to EGF stimulation in p53-induced senescent cells were intact despite their phenotypic changes (Fig. 5 B) and different from those responses in naturally senescent cells. Namely, after treatment of EGF to EJ-p53 cells, Erk-1/2 kinases were well phosphorylated as much as control proliferating cells. The ready responsiveness of EGF signaling in EJ-p53 cells regardless of the senescent phenotypic changes suggests that some different biochemical changes other than overexpression of p53 might be involved for the regulation of EGF signaling, for which we assumed that caveolin would play an important role. Therefore, we examined the expression of caveolin proteins in EJ-p53 cells, but we could not detect the overexpression of caveolin-1 proteins, which was quite different from the behavior of naturally aged cells (Fig.5 A). Moreover, an age-related increase in free cholesterol is associated with a decrease in the phospholipid content (29.Cohen B.M. Zubenko G.S. Life Sci. 1985; 37: 1403-1409Crossref PubMed Scopus (61) Google Scholar, 30.Alvarez E. Ruiz-Gutierrez V. Santa Maria C. Machado A. Mech. Ageing Dev. 1993; 71: 1-12Crossref PubMed Scopus (27) Google Scholar), which might contribute to the increased caveolin expression (31.Sargiacomo M. Scherer P.E. Tang Z. Kubler E. Song K.S. Sanders M.C. Lisanti M.P. Proc. Natl. Acad. Sci. U. S. A. 1995; 92: 9407-9411Crossref PubMed Scopus (472) Google Scholar). To know whether the aging of HDF correlates with the increasing level of cholesterol, we examined the total cholesterol in old HDF. As shown in Fig.5 C, total cholesterol level of old HDF was 1.8 times higher than young HDF. However, in the case of EJ-p53 cells, the level of cholesterol was not increased despite the induction of phenotypic senescence. The increased level of cholesterol was well matched with the up-regulation of caveolin-1 protein, both of which are the key constituents of caveolae structures. If caveolin acts dominantly in age-related attenuation of EGF signaling, the overexpression of caveolin in young fibroblast might inhibit the activation of Erk-1/2 upon EGF stimulation. To this end, we overexpressed human caveolin-1 cDNA in young HDFs and checked the activation of Erk-1/2 upon EGF stimulation. First, we examined the expression of caveolin-1 in mock- and caveolin-1-transfected cells (Fig. 6 A). After EGF stimulation of those cells, we checked the activation of Erk-1/2 by Western blot using anti-phospho-Erk antibody. As shown in Fig.6 B, the phosphorylation of Erk-1/2 was inhibited by the overexpression of caveolin-1 in young HDFs. The expression level of Erk-1/2 was not affected by transfection. These data suggest that the overexpression of caveolin-1 is sufficient to inhibit the EGF signaling in human diploid fibroblasts. Senescent cells are generally resistant not only to extrinsic noxious stimuli (32.Wang J. Walsh K. Science. 1996; 273: 359-361Crossref PubMed Scopus (459) Google Scholar, 33.Sargiacomo M. Sudol M. Tang Z. Lisanti M.P. J. Cell Biol. 1993; 122: 789-807Crossref PubMed Scopus (855) Google Scholar) but also to growth factor stimulation (2.Matsuda T. Okamura K. Sato Y. Morimoto A. Ono M. Kohno K. Kuwano M. J. Cell. Physiol. 1992; 150: 510-516Crossref PubMed Scopus (51) Google Scholar, 3.Seshadri T. Campisi J. Science. 1990; 247: 205-209Crossref PubMed Scopus (420) Google Scholar, 4.Riabowol K. Schiff J. Gilman M.Z. Proc. Natl. Acad. Sci. U. S. A. 1992; 89: 157-161Crossref PubMed Scopus (181) Google Scholar). Limited responsiveness to extrinsic and intrinsic stresses might characterize the old cells. Several hypotheses have been suggested for the mechanism involved, such as the repression of genes, modulation of signal cascades, changes in membrane properties, etc. (5.Hensler P.J. Pereira-Smith O.M. Am. J. Pathol. 1995; 147: 1-8PubMed Google Scholar, 6.Ribault D. Habib M. Abdel-Majid K. Barbara A. Mitrovic D. Mech. Ageing Dev. 1998; 100: 25-40Crossref PubMed Scopus (33) Google Scholar, 7.Peacocke M. Campisi J. J. Cell. Biochem. 1991; 45: 147-155Crossref PubMed Scopus (66) Google Scholar). However, the general mechanism or the common denominator for the unresponsiveness of the old cells has not yet been established. In this work, we have demonstrated that mechanistically caveolins or caveolae would play an important role in the regulation of signaling in the old cells. We have found that late passage old cells, either HDF or IMR-90, are enriched with all subtypes of caveolin-1, -2, and -3 and the numerous non-clathrin-coated vesicular structures. Immunoprecipitation analysis showed that caveolins were strongly bound to EGFR in the old cells, while binding was negligible in young cells, implicating the functional role in the modulation of EGF signaling in the old cells. Moreover, we showed that the overexpression of caveolin-1 in young HDF suppressed the signaling from EGF to Erk-1/2. These data strongly indicate that senescent cells are enriched with caveolae structures and caveolin proteins, which might be involved in the regulation of cellular signal transduction pathways through the direct interactions with signaling molecules. It is well known that transformed cells, including cancer cells, show a reduced level of caveolins and caveolae organelles (10.Engelman J.A. Chu C. Lin A. Jo H. Ikezu T. Okamoto T. Kohtz D.S. Lisanti M.P. FEBS Lett. 1998; 428: 205-211Crossref PubMed Scopus (346) Google Scholar, 19.Galbiati F. Volonte D. Engelman J.A. Watanabe G. Burk R. Pestell R.G. Lisanti M.P. EMBO J. 1998; 17: 6633-6648Crossref PubMed Scopus (428) Google Scholar, 34.Oka N. Yamamoto M. Schwencke C. Kawabe J. Ebina T. Ohno S. Couet J. Lisanti M.P. Ishikawa Y. J. Biol. Chem. 1997; 272: 33416-33421Abstract Full Text Full Text PDF PubMed Scopus (238) Google Scholar, 35.Lee S.W. Reimer C.L. Oh P. Campbell D.B. Schnitzer J.E. Oncogene. 1998; 16: 1391-1397Crossref PubMed Scopus (397) Google Scholar). Targeted down-regulation of caveolin-1 is sufficient to drive cell transformation and to hyperactivate the mitogen-activated protein kinase cascade, which suggests that caveolins would suppress the transformation (19.Galbiati F. Volonte D. Engelman J.A. Watanabe G. Burk R. Pestell R.G. Lisanti M.P. EMBO J. 1998; 17: 6633-6648Crossref PubMed Scopus (428) Google Scholar). The expression of caveolin-1 in CHO cells inhibits signaling from EGFR, Raf, MEK-1, and Erk-2 to the nucleus (10.Engelman J.A. Chu C. Lin A. Jo H. Ikezu T. Okamoto T. Kohtz D.S. Lisanti M.P. FEBS Lett. 1998; 428: 205-211Crossref PubMed Scopus (346) Google Scholar). The anchorage-independent growth of transformed fibroblasts also disappeared by the overexpression of caveolin-1 (36.Engelman J.A. Wykoff C.C. Yasuhara S. Song K.S. Okamoto T. Lisanti M.P. J. Biol. Chem. 1997; 272: 6374-6381Abstract Full Text Full Text PDF Scopus (334) Google Scholar). Cellular senescence was presumed to be the opposite phenomenon of the transformation. In contrast with the transformed cells, senescent cells showed reduced responsiveness, which could have been due to the elevated level of caveolins. We could successfully prove that the overexpression of caveolin-1 in young HDF directly down-regulated the phosphorylation of Erk-1/2 in response to EGF. We have compared the expression levels of caveolins in vivoto confirm our in vitro data. As summarized in Fig. 4, the organs from old animals (27 months old) showed the ubiquitous high level of caveolin-1 expression compared with those from young animals (2 months old). Interestingly, several organs, such as brain and spleen, expressed caveolin-1 protein in significantly higher amounts only in the aged state. In the cases of caveolin-2 and -3, their expressions were rather limited in an organ-specific manner, but as was the case with caveolin-1 expression, the prominent high expression in the old organs was evident. The organ-specific up-regulation of caveolins in an age-dependent manner would explain the characteristic aging process of the respective organ. For example, the high level of caveolins in the brain tissues from old animals might provide a clue to the susceptibility of elderly people to Alzheimer's disease. Since caveolin-1 promotes α-secretase processing, while caveolin-3 interacts and colocalizes with amyloid precursor protein both in vivo and in vitro, augmented expression of caveolins may alter amyloid precursor protein processing and lead to an overproduction of toxic amyloid metabolites (37.Ikezu T. Trapp B.D. Song K.S. Schlegel A. Lisanti M.P. Okamoto T. J. Biol. Chem. 1998; 273: 10485-10495Abstract Full Text Full Text PDF PubMed Scopus (139) Google Scholar, 38.Nishiyama K. Trapp B.D. Ikezu T. Ransohoff R.M. Tomita T. Iwatsubo T. Kanazawa I. Hsiao K.K. Lisanti M.P. Okamoto T. J. Neurosci. 1999; 19: 6538-6548Crossref PubMed Google Scholar). In addition, the up-regulation of caveolin with aging is suggested to relate to insulin resistance, resulting in susceptibility to diabetes mellitus (39.Munoz P. Mora S. Sevilla L. Kaliman P. Tomas E. Guma A. Testar X. Palacin M. Zorzano A. J. Biol. Chem. 1996; 271: 8133-8139Abstract Full Text Full Text PDF PubMed Scopus (46) Google Scholar). Therefore, it may be worthwhile to study the age-related degenerative disorders in association with the expression of caveolins. Recently, there have been several reports that cellular senescence can be induced by a variety of agents such as H2O2, sodium butyrate, UV irradiation, and induction of p53 or several cyclin-dependent kinase inhibitors (21.Sugrue M.M. Shin D.Y. Lee S.W. Aaronson S.A. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 9648-9653Crossref PubMed Scopus (258) Google Scholar, 23.Chen Q.M. Bartholomew J.C. Campisi J. Acosta M. Reagan J.D. Ames B.N. Biochem. J. 1998; 332: 43-50Crossref PubMed Scopus (351) Google Scholar), evaluated by irreversible growth arrest, cytomorphometry, and senescence-associated β-galactosidase activity. Although the general mechanism for induced senescence is debatable, in the genetic aspect, the forced expression of p53, as one of major senescence-associated genes, has been emphasized. Using EJ-p53 cells (21.Sugrue M.M. Shin D.Y. Lee S.W. Aaronson S.A. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 9648-9653Crossref PubMed Scopus (258) Google Scholar), we could readily induce the cellular senescence-like changes by the control of tetracycline, resembling the morphological and biochemical characteristics of naturally senescent cells. However, when the senescence was induced in EJ-p53 cells, the expressions of caveolins were not significant, while those of p53 and p21 were markedly increased (Fig. 5 A). Moreover, the downstream signal cascade of EGFR was not inhibited in senescence-induced EJ-p53 cells (Fig. 5 B). This finding proves that the down-regulation of EGFR signaling in the aged cells can be directly ascribed to the level of caveolins in one aspect and that the overexpression of p53 is not sufficient to convert the cells into the functionally senescent state in other aspect. Although caveolin-2 was induced in EJ-p53 cells, the sole expression of caveolin-2 cannot form the structurally and functionally compatible caveolae structurein vivo (27.Li S. Galbiati F. Volonté D. Sargiacomo M. Engelman J.A. Das K. Scherer P.E. Lisanti M.P. FEBS Lett. 1998; 434: 127-134Crossref PubMed Scopus (112) Google Scholar). From these results, we could reach a tentative conclusion that the expression of caveolins is essential to maintain the senescent property. It was suggested that a high level of cholesterol is required to form caveolae structure and that cholesterol plays an important role in the activation of caveolin (40.Li S. Song K.S. Lisanti M.P. J. Biol. Chem. 1996; 271: 568-573Abstract Full Text Full Text PDF PubMed Scopus (197) Google Scholar). In addition, it has been proposed that the general unresponsiveness of old cells either to growth signals or to apoptotic stimuli could be ascribed to the alteration of the cell membrane properties. Membrane lipids constantly undergo peroxidation by repeated toxic insults, and the lipid composition changes; levels of cholesterol are increased, and, inversely, phospholipid is decreased (29.Cohen B.M. Zubenko G.S. Life Sci. 1985; 37: 1403-1409Crossref PubMed Scopus (61) Google Scholar, 30.Alvarez E. Ruiz-Gutierrez V. Santa Maria C. Machado A. Mech. Ageing Dev. 1993; 71: 1-12Crossref PubMed Scopus (27) Google Scholar, 32.Wang J. Walsh K. Science. 1996; 273: 359-361Crossref PubMed Scopus (459) Google Scholar). When we checked cholesterol levels, it was found that the old HDF cells showed higher levels of cholesterol than young HDF cells (Fig. 5 C), but the senescence-induced EJ-p53 cells did not show these high levels of cholesterol. This result may provide a clue to the low level of caveolins in EJ-p53 cells. Actually, in a study of caveolin-1 gene promoter, it was reported that caveolin-1 gene promoter contains sterol regulatory element-like sequences, which are comparable with those identified in several genes for the regulation of influx and biosynthesis of cholesterol (41.Fielding C.J. Bist A. Fielding P.E. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 3753-3758Crossref PubMed Scopus (217) Google Scholar). This may explain that induction of senescence by overexpression of p53 in EJ-p53 cells is not accompanied by the high expression of caveolins, because the increase in cholesterol level does not occur. The importance of cholesterol in the regulation of caveolin expression or activation might imply the significance of nutritional intervention in the aging process. We are grateful to Dr. Sam W. Lee for helpful discussions, Dr. D Y. Shin for EJ-p53 cells, and C. J. Yoon for EM analysis. We also thank all of the members of the laboratory." @default.
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• W2023179617 title "Up-regulation of Caveolin Attenuates Epidermal Growth Factor Signaling in Senescent Cells" @default.
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