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Hyperoxia Induces Macrophage Cell Cycle Arrest by Adhesion-dependent Induction of p21Cip1 and Activation of the Retinoblastoma Protein

2003; Elsevier BV; Volume: 278; Issue: 38 Linguagem: Inglês

10.1074/jbc.m304370200

ISSN

1083-351X

Autores

Toru Nyunoya, Linda S. Powers, Timur O. Yarovinsky, Noah S. Butler, Martha M. Monick, Gary W. Hunninghake,

Tópico(s)

Cancer-related Molecular Pathways

Resumo

Hyperoxia induces growth arrest, apoptosis, necrosis, and morphological changes (spreading and adhesion) in various types of cells. The mechanism of hyperoxia-induced cell growth arrest has not been well elucidated, especially in macrophages. One possible mechanism is a role of cell adhesion in hyperoxia-induced cell cycle arrest. To evaluate this finding, macrophages were cultured in normoxia (21% O2) or hyperoxia (95% O2) in adhesion or low adhesion conditions. Incubation of macrophages in hyperoxia induced cell cycle arrest. The hyperoxia-induced cell cycle arrest was prevented by low adhesion conditions. To evaluate pathways potentially involved in hyperoxia-induced growth arrest, we measured extracellular regulated kinase and retinoblastoma protein activation and p21Cip1 and p53 accumulation. Hyperoxia strongly induced activation of extracellular regulated kinase and retinoblastoma protein as well as up-regulation of p21Cip1. These effects of hyperoxia were attenuated under low adhesion conditions, suggesting a role for integrin-dependent signaling. The induction of p21Cip1 and activation of retinoblastoma protein occurred via a p53-independent mechanism. These results suggest that adhesion-dependent pathways are required for hyperoxia-induced cell cycle arrest in macrophages. Hyperoxia induces growth arrest, apoptosis, necrosis, and morphological changes (spreading and adhesion) in various types of cells. The mechanism of hyperoxia-induced cell growth arrest has not been well elucidated, especially in macrophages. One possible mechanism is a role of cell adhesion in hyperoxia-induced cell cycle arrest. To evaluate this finding, macrophages were cultured in normoxia (21% O2) or hyperoxia (95% O2) in adhesion or low adhesion conditions. Incubation of macrophages in hyperoxia induced cell cycle arrest. The hyperoxia-induced cell cycle arrest was prevented by low adhesion conditions. To evaluate pathways potentially involved in hyperoxia-induced growth arrest, we measured extracellular regulated kinase and retinoblastoma protein activation and p21Cip1 and p53 accumulation. Hyperoxia strongly induced activation of extracellular regulated kinase and retinoblastoma protein as well as up-regulation of p21Cip1. These effects of hyperoxia were attenuated under low adhesion conditions, suggesting a role for integrin-dependent signaling. The induction of p21Cip1 and activation of retinoblastoma protein occurred via a p53-independent mechanism. These results suggest that adhesion-dependent pathways are required for hyperoxia-induced cell cycle arrest in macrophages. Hyperoxia causes damage to DNA, lipids, and proteins leading to cell cycle arrest and subsequent cell death (1Cacciuttolo M.A. Trinh L. Lumpkin J.A. Rao G. Free Radical Biol. Med. 1993; 14: 267-276Crossref PubMed Scopus (166) Google Scholar, 2Li Y. Zhang W. Mantell L.L. Kazzaz J.A. Fein A.M. Horowitz S. J. 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Chem. 1997; 272: 20646-20649Abstract Full Text Full Text PDF PubMed Scopus (92) Google Scholar, 3O'Reilly M.A. Staversky R.J. Finkelstein J.N. Keng P.C. Am. J. Physiol. 2003; 284: L368-L375Crossref PubMed Scopus (33) Google Scholar, 4Helt C.E. Rancourt R.C. Staversky R.J. O'Reilly M.A. Toxicol. Sci. 2001; 63: 214-222Crossref PubMed Scopus (72) Google Scholar, 5Rancourt R.C. Hayes D.D. Chess P.R. Keng P.C. O'Reilly M.A. J. Cell. Physiol. 2002; 193: 26-36Crossref PubMed Scopus (56) Google Scholar, 6Rancourt R.C. Keng P.C. Helt C.E. O'Reilly M.A. Am. J. Physiol. 2001; 280: L617-L626Crossref PubMed Google Scholar) and endothelial cells (8Martin II, W.J. Kachel D.L. J. Lab. Clin. Med. 1989; 113: 413-421PubMed Google Scholar, 9Junod A.F. Petersen H. Jornot L. J. Appl. Physiol. 1987; 62: 10-14Crossref PubMed Scopus (15) Google Scholar); however, little is known regarding the effects of hyperoxia on macrophages. What has been described is the effect of hyperoxia on stimulus-induced cytokine production (10Desmarquest P. Chadelat K. Corroyer S. Cazals V. Clement A. Respir. Med. 1998; 92: 951-960Abstract Full Text PDF PubMed Scopus (51) Google Scholar) and hyperoxia-induced cell spreading associated with the effects on actin (13O'Reilly P.J. Hickman-Davis J.M. Davis I.C. Matalon S. Am. J. Respir. Cell Mol. Biol. 2003; 28: 443-450Crossref PubMed Scopus (62) Google Scholar). Animal models have shown that hyperoxia induces recruitment of macrophages to the lungs (11Coalson J.J. King R.J. Winter V.T. Prihoda T.J. Anzueto A.R. Peters J.I. Johanson Jr., W.G. J. Appl. Physiol. 1989; 67: 346-356Crossref PubMed Scopus (36) Google Scholar) but decreases antibacterial function (12Suttorp N. Simon L.M. Am. Rev. Respir. Dis. 1983; 128: 486-490Crossref PubMed Scopus (23) Google Scholar, 13O'Reilly P.J. Hickman-Davis J.M. Davis I.C. Matalon S. Am. J. Respir. Cell Mol. Biol. 2003; 28: 443-450Crossref PubMed Scopus (62) Google Scholar) and cell migration (14Bowles A.L. Dauber J.H. Daniele R.P. Am. Rev. Respir. Dis. 1979; 120: 541-545PubMed Google Scholar). In this study, we evaluated the effect of hyperoxia on macrophage proliferation and cell cycle regulation. In contrast to macrophages, more is known regarding the effects of hyperoxia on epithelial cells. In epithelial cells, hyperoxia inhibits proliferation through activation of cell cycle checkpoints until DNA damage is repaired. This phenomenon is critical for maintaining genomic integrity (3O'Reilly M.A. Staversky R.J. Finkelstein J.N. Keng P.C. Am. J. Physiol. 2003; 284: L368-L375Crossref PubMed Scopus (33) Google Scholar, 5Rancourt R.C. Hayes D.D. Chess P.R. Keng P.C. O'Reilly M.A. J. Cell. Physiol. 2002; 193: 26-36Crossref PubMed Scopus (56) Google Scholar, 15Corroyer S. Maitre B. Cazals V. Clement A. J. Biol. Chem. 1996; 271: 25117-25125Abstract Full Text Full Text PDF PubMed Scopus (75) Google Scholar). Various proteins are known to be key regulators of the cell cycle, including cyclins, cyclin-dependent kinases (CDK), 1The abbreviations used are: CDK, cyclin-dependent kinases; CKI, CDK inhibitors; MAPK, mitogen-activated protein kinase; ERK, extracellular signal-regulated kinase; Rb, retinoblastoma; RT, reverse transcription; Ct, threshold cycle; STAT, signal transducers and activators of transcription; INK4, inhibitors of cyclin-dependent kinase 4; HPRT, hypoxantine-guanine phosphoribosyltransferase. and CDK inhibitors (CKI). Cyclin-CDK complexes positively regulate cell cycle progression and are negatively controlled by CKIs (16Pavletich N.P. J. Mol. Biol. 1999; 287: 821-828Crossref PubMed Scopus (566) Google Scholar, 17Morgan D.O. Annu. Rev. Cell Dev. Biol. 1997; 13: 261-291Crossref PubMed Scopus (1804) Google Scholar). CKIs are divided into two classes on the basis of their homology, the Kip/Cip family (p21Cip1, p27Kip1, and p57Kip2) and the INK4 family (p16INK4a, p15INK4b, p18INK4C, and p19INK4d). The Kip/Cip family inhibits a broad range of CDKs (17Morgan D.O. Annu. Rev. Cell Dev. Biol. 1997; 13: 261-291Crossref PubMed Scopus (1804) Google Scholar, 18Sherr C.J. Roberts J.M. Genes Dev. 1999; 13: 1501-1512Crossref PubMed Scopus (5145) Google Scholar). Increases in p21Cip1 (p21) have been shown to play a central role in hyperoxia-induced growth arrest (19McGrath S.A. Am. J. Respir. Cell Mol. Biol. 1998; 18: 179-187Crossref PubMed Scopus (59) Google Scholar, 20Shenberger J.S. Dixon P.S. Am. J. Respir. Cell Mol. Biol. 1999; 21: 395-402Crossref PubMed Scopus (64) Google Scholar, 21O'Reilly M.A. Staversky R.J. Watkins R.H. Maniscalco W.M. Am. J. Respir. Cell Mol. Biol. 1998; 19: 777-785Crossref PubMed Scopus (61) Google Scholar). p21 has also been shown to play a crucial role in cell cycle control in response to the other stimuli such as glucocorticoids (22Corroyer S. Nabeyrat E. Clement A. Endocrinology. 1997; 138: 3677-3685Crossref PubMed Scopus (45) Google Scholar) and cigarette smoke (23Marwick J.A. Kirkham P. Gilmour P.S. Donaldson K. Macnee W. Rahman I. Ann. N. Y. Acad. Sci. 2002; 973: 278-283Crossref PubMed Scopus (53) Google Scholar). In lung epithelial cells, a marked increase in p21 has been observed after oxygen exposure (15Corroyer S. Maitre B. Cazals V. Clement A. J. Biol. Chem. 1996; 271: 25117-25125Abstract Full Text Full Text PDF PubMed Scopus (75) Google Scholar). A study by Corroyer et al. (15Corroyer S. Maitre B. Cazals V. Clement A. J. Biol. Chem. 1996; 271: 25117-25125Abstract Full Text Full Text PDF PubMed Scopus (75) Google Scholar) found that one target of p21 action was the cyclin E-CDK2 complex that facilitates cell cycle progression to the S phase (15Corroyer S. Maitre B. Cazals V. Clement A. J. Biol. Chem. 1996; 271: 25117-25125Abstract Full Text Full Text PDF PubMed Scopus (75) Google Scholar). Induction of p21 can occur via p53-dependent (24Dulic V. Kaufmann W.K. Wilson S.J. Tlsty T.D. Lees E. Harper J.W. Elledge S.J. Reed S.I. Cell. 1994; 76: 1013-1023Abstract Full Text PDF PubMed Scopus (1417) Google Scholar, 25el-Deiry W.S. Harper J.W. O'Connor P.M. Velculescu V.E. Canman C.E. Jackman J. Pietenpol J.A. Burrell M. Hill D.E. Wang Y. et al.Cancer Res. 1994; 54: 1169-1174PubMed Google Scholar) and p53-independent mechanisms (26Biggs J.R. Kudlow J.E. Kraft A.S. J. Biol. Chem. 1996; 271: 901-906Abstract Full Text Full Text PDF PubMed Scopus (199) Google Scholar, 27Zeng Y.X. Somasundaram K. el-Deiry W.S. Nat. Genet. 1997; 15: 78-82Crossref PubMed Scopus (260) Google Scholar, 28Chin Y.E. Kitagawa M. Su W.C. You Z.H. Iwamoto Y. Fu X.Y. Science. 1996; 272: 719-722Crossref PubMed Scopus (730) Google Scholar, 29Chinery R. Brockman J.A. Peeler M.O. Shyr Y. Beauchamp R.D. Coffey R.J. Nat. Med. 1997; 3: 1233-1241Crossref PubMed Scopus (336) Google Scholar). Induction of p21 independent of p53 has been reported in hyperoxia conditions (30O'Reilly M.A. Staversky R.J. Watkins R.H. Reed C.K. de Mesy Jensen K.L. Finkelstein J.N. Keng P.C. Am. J. Respir. Cell Mol. Biol. 2001; 24: 703-710Crossref PubMed Scopus (101) Google Scholar). Hyperoxia induces morphological changes including cell spreading (13O'Reilly P.J. Hickman-Davis J.M. Davis I.C. Matalon S. Am. J. Respir. Cell Mol. Biol. 2003; 28: 443-450Crossref PubMed Scopus (62) Google Scholar). Previously, we reported that cell adhesion (integrin signaling) was required for lipopolysaccharide-induced activation of the mitogen-activated kinase (MAPK), extracellular regulated kinase (ERK), and optimal tumor necrosis factor-α production (31Monick M.M. Powers L. Butler N. Yarovinsky T. Hunninghake G.W. Am. J. Physiol. 2002; 283: L390-L402PubMed Google Scholar). In this study, we evaluated the role of adhesion (tissue culture plates and extracellular matrix-coated plates with collagen type I, collagen type IV, or fibronectin) on hyperoxia-induced growth arrest in macrophages. The studies show that growth arrest was accompanied by increased amounts of macrophage spreading, ERK activation, p21 induction, and retinoblastoma protein (Rb) activation. These effects of hyperoxia occurred via a p53-independent mechanism and were reversed by blocking cell adhesion. These data suggest that hyperoxia-induced growth arrest requires an integrin-dependent signal. Reagents and Antibodies—Chemicals were obtained from Sigma. Protease inhibitors were obtained from Roche Applied Science. Nitrocellulose filters and ECL Plus were obtained from Amersham Biosciences. Antibodies were obtained from various sources. Anti-p21 was from Santa Cruz Biotechnology (Santa Cruz, CA), and phosphorylation-specific antibodies for ERK and Rb were from Cell Signaling (Beverly, MA). Developing antibodies (horseradish peroxidase-conjugated anti-rabbit or anti-mouse Ig) were obtained from Santa Cruz Biotechnology. Tissue culture plates and special adherence-free plates (Teflon-coated Ultra Low Attachment) were obtained from Corning (Corning, NY). Extracellular matrix-coated plates with collagen type I, collagen type IV, or fibronectin were obtained from BD Biosciences (Bedford, MA). Cell Culture and Cell Proliferation—RAW264.7 cells (TIB-71, American Type Culture Collection) were maintained at 37 °C and in Dulbecco's modified Eagle's medium (high glucose) with 10% fetal bovine serum and gentamicin (40 μg/ml). Cells were subcultured every 2–3 days. Experiments were performed in six-well (35 mm) Costar tissue culture plates (low-adherence or standard) or extracellular matrix-coated (collagen type I, collagen type IV, or fibronectin) plates (35 mm) under normoxia (FiO2 = 21%) or in hyperoxia (FiO2 = 95%) at the starting cell density of 0.5 × 106/ml. The cells were removed by scraping, suspended in the original medium, and centrifuged at 300 × g. The cells were resuspended in 3 ml of 1× Dulbecco's phosphate-buffered saline and counted with an electric particle counter (Coulter Electronics, Hialeah, FL). Isolation of Whole Cell Extracts—Whole cell protein was obtained by lysing the cells on ice for 20 min in 500 μl of lysis buffer (0.05 m Tris, pH 7.4, 0.15 m NaCl, 1% Nonidet P-40, 0.5 m phenylmethylsulfonyl fluoride, 50 μg/ml aprotinin, 10 μg/ml leupeptin, 50 μg/ml pepstatin, 0.4 mm sodium orthovanadate, 10 mm sodium fluoride, and 10 mm sodium pyrophosphate; all from Roche Applied Science). The lysates were then sonicated for 20 s, incubated on ice for 30 min, and centrifuged at 15,000 × g for 10 min at 4 °C. Protein was quantified using a protein measurement kit (protein assay kit 500-0006, Bio-Rad). Cell lysates were stored at −70 °C until use. Western Blot Analysis—Western blot analysis for the presence of particular proteins or for phosphorylated forms of proteins was performed on whole cell proteins. Protein (30–80 μg) was mixed 1:1 with 2× sample buffer (20% glycerol, 4% SDS, 10% mercaptoethanol, 0.05% bromphenol blue, and 1.25 m Tris, pH 6.8; all from Sigma), heated to 95 °C for 5 min, and fractionated on a 10 or 12.5% SDS-polyacrylamide gel run at 100 V for 90 min. Cell proteins were transferred to nitrocellulose filters (ECL) by semidry transfer (Bio-Rad) at 20 V for 45 min. Equal loading of the protein groups on the blots was evaluated by using Ponceau S, a staining solution designed for staining proteins on nitrocellulose membranes (Sigma). The nitrocellulose filter was blocked with 5% milk in Tris-buffered saline with 0.1% Tween 20 for 1 h, washed, and then incubated with the primary antibody overnight. The blots were washed four times with Tris-buffered saline with Tween 20 and incubated for 1 h with horseradish peroxidase-conjugated anti-rabbit or anti-mouse IgG antibody. Immunoreactive bands were developed using a chemiluminescent substrate (ECL Plus or SuperSignal West Femto). An autoradiograph was obtained with exposure times of 10 s to 2 min. Flow Cytometry—RAW264.7 cells were cultured in conditions of normoxia (21% O2) or hyperoxia (95% O2 and 5% CO2) on adhesion plates or low adhesion plates for 24 h. The cells were washed twice in phosphate-buffered saline and fixed in cold 70% ethanol overnight. After two washes in phosphate-buffered saline, the cells were treated with 0.25 mg/ml RNase A (Roche Applied Science) and stained with 50 μg/ml propidium iodide at 4 °C for 30 min in the dark and analyzed for DNA content. A total of 10,000 cells that satisfied a gate on forward and side scatter to eliminate aggregates and debris were evaluated with a FACScan flow cytometer (BD Biosciences). Data analysis was performed with ModFit LT (Verity Software House Inc, Topsham, ME). Real-time RT-PCR—Total RNA was isolated using the Absolutely RNA RT-PCR miniprep kit (Stratagene, La Jolla, CA) following the manufacturer's instructions. RNA was quantitated using RiboGreen Kit (Molecular Probes, Eugene, OR). 1 μg of total RNA was reverse-transcribed to cDNA using RETROscript RT-PCR kit (Ambion, Austin, TX). In a 0.2-ml PCR tube (Bio-Rad), 2 μl of cDNA (10% cDNA synthesis reaction volume) was added to 48 μl of PCR reaction mixture containing 160 μm each dNTP (Invitrogen), 3.0 mm MgCl2 (Invitrogen), 1:10,000 SYBR Green I DNA dye (Molecular Probes), 0.2 μm of each sense and antisense primers (IDT, Coralville, IA), and 2.5 units of Platinum TaqDNA polymerase (Invitrogen). Amplification was then performed in an iCycler iQ Fluorescence Thermocyler (Bio-Rad) as follows: 5 min at 95 °C followed by 45 cycles of 20 s at 95 °C, 20 s at 60 °C, and 20 s at 72 °C. Fluorescence data were captured during the 72 °C dwell time. Specificity of the amplification was confirmed using melting curve analysis. Data were collected and recorded by iCycler iQ software (Bio-Rad) and expressed as a function of threshold cycle (Ct), the cycle at which the fluorescence intensity in a given reaction tube rises above background (calculated as 10 times the mean ± S.D. of fluorescence in all of the wells over the base-line cycles). Specific primer sets used are as follows (5′ to 3′): p21 sense, TCCACAGCGATATCCAGACA; p21 antisense, CAGGGCAGAGGAAGTACTGG; HPRT sense, CCTCATGGACTGATTATGGAC; and HPRT antisense, CAGATTCAACTTGCGCTCATC. Primers were selected based on nucleotide sequences downloaded from the National Center for Biotechnology Information data bank and designed with software by Steve Rozen and Helen J. Skaletsky (1998 Primer3, code available at www-genome.wi.mit.edu/genome_software/other/primer3.html). Quantitative Gene Expression—Quantitative p21 mRNA expression was calculated as follows. For each sample assayed, the Ct for reactions amplifying p21 and the HPRT housekeeping gene were determined. The p21 Ct for each sample was corrected by subtracting the Ct for HPRT (ΔCt). Finally, p21 mRNA abundance, relative to HPRT mRNA abundance, was calculated by the formula 2−(ΔCt). Validity of this approach was confirmed by using serial 10-fold dilutions of template for p21 and HPRT. Using the 10-fold dilutions, the amplification efficiencies for p21 and HPRT were found to be identical. Statistical Analysis—The results were expressed as the mean ± S.E. The number of cells in each condition at various time points in adherence or non-adherence conditions was compared using a unpaired Student's t test. Hyperoxia Induces Macrophage Growth Arrest—To investigate the effects of hyperoxia on RAW264.7 cells (macrophages), we performed the following experiments. Macrophages were cultured in standard tissue culture plates and extracellular matrix-coated (collagen type I, collagen type IV, or fibronectin) plates under conditions of normoxia (21% O2) or hyperoxia (95% O2) at the starting cell density of 0.5 × 106/ml. Cell counts were measured at various time points as described under "Experimental Procedures." As shown in Fig. 1A, hyperoxia-induced cell growth arrest was significant at 24 and 48 h (p < 0.05) in both standard tissue culture plates and extracellular matrix-coated plates with collagen type I, collagen type IV, or fibronectin. Fig. 1B shows morphological changes demonstrating a greater degree of cell spreading in the hyperoxia group on all of the substrates at 48 h. These studies show that hyperoxia decreases cell proliferation and induces morphological changes in macrophages. Hyperoxia-induced Growth Arrest Requires Cell Adhesion— Because hyperoxia induced marked morphological changes associated with cell spreading (13O'Reilly P.J. Hickman-Davis J.M. Davis I.C. Matalon S. Am. J. Respir. Cell Mol. Biol. 2003; 28: 443-450Crossref PubMed Scopus (62) Google Scholar), we postulated that an increase in cell adhesion by hyperoxia might contribute to cell growth arrest. To evaluate this possibility, macrophages were cultured in normoxia (21% O2) or hyperoxia (95% O2) in standard tissue culture plates or low adherence plates. The number of cells was measured at 2, 24, and 48 h. As shown in Fig. 2A, low adhesion conditions blocked hyperoxia-induced cell growth arrest. These results suggest that hyperoxia-induced cell growth arrest is dependent on cell adhesion. Hyperoxia Induces Growth Arrest at the G 0/G 1 Phase of the Cell Cycle—Hyperoxia has been reported to induce cell cycle arrest and apoptosis or necrosis (1Cacciuttolo M.A. Trinh L. Lumpkin J.A. Rao G. Free Radical Biol. Med. 1993; 14: 267-276Crossref PubMed Scopus (166) Google Scholar, 2Li Y. Zhang W. Mantell L.L. Kazzaz J.A. Fein A.M. Horowitz S. J. Biol. Chem. 1997; 272: 20646-20649Abstract Full Text Full Text PDF PubMed Scopus (92) Google Scholar, 3O'Reilly M.A. Staversky R.J. Finkelstein J.N. Keng P.C. Am. J. Physiol. 2003; 284: L368-L375Crossref PubMed Scopus (33) Google Scholar, 4Helt C.E. Rancourt R.C. Staversky R.J. O'Reilly M.A. Toxicol. Sci. 2001; 63: 214-222Crossref PubMed Scopus (72) Google Scholar, 5Rancourt R.C. Hayes D.D. Chess P.R. Keng P.C. O'Reilly M.A. J. Cell. Physiol. 2002; 193: 26-36Crossref PubMed Scopus (56) Google Scholar, 6Rancourt R.C. Keng P.C. Helt C.E. O'Reilly M.A. Am. J. Physiol. 2001; 280: L617-L626Crossref PubMed Google Scholar, 7Schoonen W.G. Wanamarta A.H. van der Klei-van Moorsel J.M. Jakobs C. Joenje H. Mutat. Res. 1990; 237: 173-181Crossref PubMed Scopus (43) Google Scholar, 32Petrache I. Choi M.E. Otterbein L.E. Chin B.Y. Mantell L.L. Horowitz S. Choi A.M. Am. J. Physiol. 1999; 277: L589-L595Crossref PubMed Google Scholar). To determine whether hyperoxia induced adhesion-dependent cell cycle arrest, we performed flow cytometry with DNA staining by propidium iodide. Cell cycle was analyzed at 24 h with four conditions, adhesion conditions with normoxia (21% O2) or hyperoxia (95% O2) and low adhesion conditions with normoxia or hyperoxia. Cell cycle analysis showed that hyperoxia induced a significant decrease in the S phase at 24 h (Fig. 2B) associated with cell cycle arrest at the G0/G1 phase (data not shown). There was no evidence for apoptosis in hyperoxia conditions up to 48 h (data not shown). Taken together, the data show that hyperoxia induces an adherence-dependent G1 phase cell growth arrest with limited cell death. Hyperoxia Induces ERK Activity That Is Dependent on Adhesion—Hyperoxia has been shown to induce the activation of ERK MAPK (32Petrache I. Choi M.E. Otterbein L.E. Chin B.Y. Mantell L.L. Horowitz S. Choi A.M. Am. J. Physiol. 1999; 277: L589-L595Crossref PubMed Google Scholar). Previously, we showed that cell adhesion was necessary to induce optimal activation of ERK in macrophages stimulated by lipopolysaccharide (31Monick M.M. Powers L. Butler N. Yarovinsky T. Hunninghake G.W. Am. J. Physiol. 2002; 283: L390-L402PubMed Google Scholar). Based on these observations, we hypothesized that hyperoxia-induced activation of ERK might be attenuated by low adhesion. To evaluate this hypothesis, macrophages were cultured in adhesion or low adhesion conditions with normoxia (21% O2) or hyperoxia (95% O2). Western blot analysis was performed for phosphorylation of ERK. Hyperoxia induced a sustained markedly increased phosphorylation of ERK in cells cultured in adhesion conditions (Fig. 3A). Notably, low adhesion reversed the hyperoxia-induced ERK activity as shown in Fig. 3B. Pharmacological inhibition of ERK led to hyperoxia-induced cell death (data not shown), not increased cell proliferation. This finding suggests that the cell cycle arrest is not the result of the hyperoxia induced ERK activity and that other hyperoxia-inducible factors may play a role in cell cycle arrest. As a composite, these data suggest that hyperoxia-induced ERK activation is adhesion-dependent and may play a role in cell survival in hyperoxia conditions but is not linked to the cell cycle arrest demonstrated in Figs. 1 and 2. Hyperoxia Induces Cell Cycle Arrest via an Adhesion-dependent Induction of p21—Hyperoxia has been shown to induce cell growth arrest by CKIs (3O'Reilly M.A. Staversky R.J. Finkelstein J.N. Keng P.C. Am. J. Physiol. 2003; 284: L368-L375Crossref PubMed Scopus (33) Google Scholar, 4Helt C.E. Rancourt R.C. Staversky R.J. O'Reilly M.A. Toxicol. Sci. 2001; 63: 214-222Crossref PubMed Scopus (72) Google Scholar, 5Rancourt R.C. Hayes D.D. Chess P.R. Keng P.C. O'Reilly M.A. J. Cell. Physiol. 2002; 193: 26-36Crossref PubMed Scopus (56) Google Scholar, 6Rancourt R.C. Keng P.C. Helt C.E. O'Reilly M.A. Am. J. Physiol. 2001; 280: L617-L626Crossref PubMed Google Scholar, 30O'Reilly M.A. Staversky R.J. Watkins R.H. Reed C.K. de Mesy Jensen K.L. Finkelstein J.N. Keng P.C. Am. J. Respir. Cell Mol. Biol. 2001; 24: 703-710Crossref PubMed Scopus (101) Google Scholar), and p21 is a major CKI linked to cell growth arrest at the G1 phase (33Harper J.W. Elledge S.J. Keyomarsi K. Dynlacht B. Tsai L.H. Zhang P. Dobrowolski S. Bai C. Connell-Crowley L. Swindell E. Mol. Biol. Cell. 1995; 6: 387-400Crossref PubMed Scopus (860) Google Scholar, 34Deng C. Zhang P. Harper J.W. Elledge S.J. Leder P. Cell. 1995; 82: 675-684Abstract Full Text PDF PubMed Scopus (1948) Google Scholar). For these reasons, we analyzed the effect of hyperoxia on p21 accumulation. Macrophages were cultured in adherence or non-adherence conditions with normoxia (21% O2) or hyperoxia (95% O2). Western blot analysis and mRNA quantification were performed for p21. As shown in Fig. 4, A and B, hyperoxia induced accumulation of both p21 protein and mRNA and this was blocked by low adhesion. We also performed Western blot analysis for p53, which can under some conditions be upstream of p21. The accumulation of p21 was independent of p53, because hyperoxia decreased amounts of p53 (Fig. 4C). These results demonstrate that hyperoxia induces an adhesion-dependent induction of p21, which is independent of p53. Hyperoxia Increases Rb Hypophosphorylation in an Adhesiondependent Manner—Phosphorylation of Rb decreases its ability to cause cell cycle arrest. p21 induces cell cycle arrest, in part, by decreasing phosphorylation of Rb (17Morgan D.O. Annu. Rev. Cell Dev. Biol. 1997; 13: 261-291Crossref PubMed Scopus (1804) Google Scholar, 18Sherr C.J. Roberts J.M. Genes Dev. 1999; 13: 1501-1512Crossref PubMed Scopus (5145) Google Scholar). For this reason, we postulated that hyperoxia-induced p21 accumulation would lead to hypophosphorylation of Rb. Macrophages were cultured in adherence or non-adherence conditions with normoxia (21% O2) or hyperoxia (95% O2). Western blot analysis was performed to determine the phosphorylation state of Rb. As shown in Fig. 5, hyperoxia decreased phosphorylation of Rb. The increase in hypophosphorylated Rb did not occur in low adhesion conditions. These results are consistent with the p21 data and cell cycle analyses shown above. As a composite, the data suggest that hyperoxia requires adhesion-dependent signals to induce p21, activate Rb, and cause cell cycle arrest. This study demonstrates that in macrophages, hyperoxia inhibits cell proliferation and induces morphological changes such as cell spreading. Hyperoxia-induced growth arrest occurred in both standard tissue culture plates and extracellular matrix-coated plates with collagen type I, collagen type IV, or fibronectin. The hyperoxia-induced growth arrest was accompanied by p21 induction and Rb activation. All of these observations were dependent on cell adhesion as cells cultured in low adhesion conditions continued to proliferate and did not increase p21 or Rb activity. The effects were not dependent on p53 activity. Interestingly, hyperoxia induced ERK activity and this was blocked by low adhesion conditions. Inhibition of ERK activity, however, did not reverse the growth arrest but facilitated cell death, suggesting that hyperoxia-induced ERK was important for cell survival under hyperoxia conditions. As a composite, these data show that in macrophages, hyperoxia/adherence induces cell survival in part via an effect on ERK MAPK and cell cycle arrest via an effect of p21 induction and Rb activation. A number of studies have evaluated the effects of hyperoxia on cell cycle in non-macrophage cell lines. It has been reported that hyperoxia inhibits cell proliferation and induces cell death in A549 epithelial cells (2Li Y. Zhang W. Mantell L.L. Kazzaz J.A. Fein A.M. Horowitz S. J. Biol. 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In this regard, hyperoxia has been shown to induce p53 in proliferating but not in confluent Mv1Lu adenocarcinoma cells (5Rancourt R.C. Hayes D.D. Chess P.R. Keng P.C. O'Reilly M.A. J. Cell. Physiol. 2002; 193: 26-36Crossref PubMed Scopus (56) Google Scholar). One possible upstream inducer of p53-independent p21 is the ERK MAPK. Several studies have demonstrated that highly activated Raf-1 elicited p53-independent induction of p21 and cell cycle arrest in murine NIH 3T3 cells (48Sewing A. Wiseman B. Lloyd A.C. Land H. Mol. Cell. Biol. 1997; 17: 5588-5597Crossref PubMed Scopus (419) Google Scholar, 49Woods D. Parry D. Cherwinski H. Bosch E. Lees E. McMahon M. Mol. Cell. Biol. 1997; 17: 5598-5611Crossref PubMed Scopus (576) Google Scholar). Sustained activation of MAPK through activated Raf-1 has been also shown to result in induction of p21 transcription and cell cycle arrest in NIH 3T3 cells (50Pumiglia K.M. Decker S.J. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 448-452Crossref PubMed Scopus (328) Google Scholar). This finding suggests that the hyperoxia/adhesion-dependent activation of the ERK MAPK pathway may contribute to the p53-independent induction of p21. The eukaryotic cell cycle is traditionally divided into four phases, a gap phase (G0/G1), a synthesis phase (S), a second gap phase (G2), and mitosis (M). The retinoblastoma tumor suppressor protein (Rb) is a key player in cell cycle arrest at the G1/S phase (18Sherr C.J. Roberts J.M. Genes Dev. 1999; 13: 1501-1512Crossref PubMed Scopus (5145) Google Scholar, 51Bartek J. Bartkova J. Lukas J. Exp. Cell Res. 1997; 237: 1-6Crossref PubMed Scopus (230) Google Scholar, 52Sherr C.J. Science. 1996; 274: 1672-1677Crossref PubMed Scopus (4977) Google Scholar). The activity of Rb is down-regulated by phosphorylation (18Sherr C.J. Roberts J.M. Genes Dev. 1999; 13: 1501-1512Crossref PubMed Scopus (5145) Google Scholar). Activation or hypophosphorylation of Rb can be induced through p21-dependent (53Bai F. Matsui T. Ohtani-Fujita N. Matsukawa Y. Ding Y. Sakai T. FEBS Lett. 1998; 437: 61-64Crossref PubMed Scopus (54) Google Scholar) or p21-independent pathways (54Cicchillitti L. Fasanaro P. Biglioli P. Capogrossi M.C. Martelli F. J. Biol. Chem. 2003; 278: 19509-19517Abstract Full Text Full Text PDF PubMed Scopus (99) Google Scholar). Cicchillitti et al. (54Cicchillitti L. Fasanaro P. Biglioli P. Capogrossi M.C. Martelli F. J. Biol. Chem. 2003; 278: 19509-19517Abstract Full Text Full Text PDF PubMed Scopus (99) Google Scholar) describe oxidative-induced hypophosphorylation of Rb not dependent on p21 but on the activity of protein phosphatase 2A in human umbilical vein endothelial cells (54Cicchillitti L. Fasanaro P. Biglioli P. Capogrossi M.C. Martelli F. J. Biol. Chem. 2003; 278: 19509-19517Abstract Full Text Full Text PDF PubMed Scopus (99) Google Scholar). In contrast, the G1 phase arrest by flavone, anti-proliferative agent derived from plants, is because of p53-independent transcriptional induction of the p21 gene and the subsequent hypophosphorylation of Rb in A549 cells (53Bai F. Matsui T. Ohtani-Fujita N. Matsukawa Y. Ding Y. Sakai T. FEBS Lett. 1998; 437: 61-64Crossref PubMed Scopus (54) Google Scholar). We found that activation of Rb was induced with p21 accumulation in an adhesion-dependent manner under conditions of hyperoxia. In conclusion, this study demonstrates that hyperoxia induces cell cycle arrest that is dependent on cell adhesion. Hyperoxia induces both p21 accumulation and Rb activation, also in an adhesion-dependent manner. Hyperoxia also induces ERK activation via an adhesion-dependent mechanism that was linked to cell survival under hyperoxia conditions. The novel observations of this study, adhesion-dependent induction of p21 protein, activation of Rb, and cell cycle arrest suggests a previously unknown role for integrin signaling in macrophage responses to hyperoxia.

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