Reduced pulmonary function is age-dependent in the rat lung in normoxia
© I. Holzapfel Publishers 2010
Published: 4 November 2010
Oxygen transport is optimized at the cellular level, since oxygen serves as the terminal electron acceptor in mitochondrial oxidative phosphorylation and several enzymatic processes require molecular oxygen as substrate. During development and aging, redundant cells and exhausted cells are eliminated, respectively, whereas others can adapt to the stressful environment and survive.
The study investigated the molecular mechanisms activated in the lung during normal aging, through the expression of hypoxia inducible factor (HIF), vascular endothelial growth factor (VEGF), p53, p66Shc, putative cysteine protease (CPP32) and kinaseB-α phosphorylation (pIkB-α).
Materials and methods
Twelve male Wistar rats divided into two age-groups, each consisting of 6 animals, 3 and 24 months old, were used. The rats were anesthetized with Nembutal (40 mg/kg, ip) and the lungs were excised from each rat and processed for TUNEL and Western blotting analyses.
The expressions of p53, p66Shc and CPP32 were significantly increased in the old normoxic rat lung specimens, when compared with the young ones. In parallel, expressions of VEGF and pIkBα were increased in old rather than young rats.
Aging leads to increased expressions of p53, p66Shc and CPP32, suggesting that apoptosis is in progress. At the same time, the lung tries to counteract apoptosis through the production of VEGF and pIkB-α to adapt itself to a stressful situation. The aging lung creates a life-support system in order to counteract the apoptotic process.
The lung is the essential respiratory organ in all air-breathing animals and its principal function is to transport oxygen from the atmosphere into the bloodstream and to release carbon dioxide from the bloodstream into the atmosphere. Normally, the partial pressure of oxygen (PO2) decreases from the lung to mitochondria with the changing distance of oxygen diffusion to tissues . To counteract the low availability of oxygen, which is the most physiological stimulus for angiogenesis , cells reorganize themselves through the angiogenesis and subsequent remodeling while the oxygen transport is optimized, since oxygen serves as the terminal electron acceptor in mitochondrial oxidative phosphorylation and several enzymatic processes require molecular oxygen as substrate. Functionality of the lung is related to aging, which is a physiological condition characterized by a modification of structure and geometry of tissues which undergo a progressive lost in elasticity (i.e., in both blood vessels and pulmonary tissue) and by a general reduction of the homeostatic capacity along with a decrease in oxygen supply to tissues. During aging the diffusion distance between the lung and mitochondria elongates along with a progressive decrease in maximum consumption of oxygen (VO2max). The regulation of pulmonary function and its adaptive capacity depends on specific feedback mechanisms initiated by chemoreceptors. The molecular mechanism of cell sensitivity to oxygen is still unknown . During development and aging, redundant cells and exhausted cells are eliminated, respectively, whereas other cells can adapt to the stressful environment and survive. The factors that determine the fate of each cell are probably influenced by the main mechanism regulating gene expression . Upon interaction with an external stimulus, such a mechanism involves a series of chemical steps that transduce signals into the nucleus and lead to induction or repression of transcription [5, 6]. This can bring about apoptosis [7, 8] of exhausted cells during aging  or those injured by oxidative stress .
Since aging is a condition in which there already is a decrease of oxygen supply to tissue, the hypothesis of this work was that the lung could be able to create a life-support system, adapting to stressful situations caused by reduced oxygen supply to tissue. Among the molecules involved in such a mechanism, a role has been assigned to p53 [11, 12]. The p53 tumor suppressor protein triggers cell cycle arrest and apoptosis in response to cellular stresses such as DNA damage, hypoxia and oncogene activation. In particular, this molecule seems to play a role in stabilizing hypoxia-inducible factor-1α (HIF-1α) [13, 14]. HIF-1α DNA-binding protein is a heterodimer composed of two subunits: HIF-1β, which can dimerize with different basic helix-loop-helix PAS proteins, and HIF-1α, which is the O2-regulated subunit that determines the biological activity of the molecule. Thus, the aim of this work has been to investigate the molecular mechanism activated during aging by the lung, through the expression of p53 and HIF-1α, but also of vascular endothelial growth factor (VEGF) which gives a signal produced by cells to stimulate the growth of new blood vessels, part of the response aimed at restoring oxygen supply to tissue when blood circulation is inadequate, p66Shc which is a protein that translates oxidative damage into cell apoptosis and increases upon apoptotic stimulation in a p53-dependent way , caspase-3 (CPP32) which is a prototypical caspase that becomes activated during apoptosis , and kinaseB-α phosphorylation (pIkB-α), an important molecule involved in cellular survival pathways by inhibiting apoptotic processes.
Materials and methods
Two groups, each composed of 6 male Wistar rats, three-months (weight 200-250 g) and twenty-four (weight 350-400 g) months old, were used according to the guidelines of the Declaration of Helsinki for care and use of experimental animals. Only animals free of acute and chronic illness were employed. The rats were anesthetized with Nembutal (40 mg/kg, i.p.) and the lungs, excised from each rat, was processed for TUNEL and Western blotting analysis. In parallel we have also applied a hypoxic condition (8% O2) for the same number of animals for the same days (data and results not shown in this article).
Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling (TUNEL) is a method of choice for a rapid identification and quantification of apoptotic cells. DNA strand breaks, yielded during apoptosis, can be identified by labeling free 3'-OH terminals with modified nucleotides in an enzymatic reaction. Paraffin-embedded tissue sections (dewaxed, re-hydrated, and preincubated with proteinase K 20 μg/ml in 10 mmol/l Tris-HCl at pH 7.6) were exposed to the TUNEL mixture according to the manufacturer's instructions (Boehringer Mannheim, Germany). After two rinses in phosphate-buffered saline, the slides were mounted by using a propidium iodide-glycerol solution (10 μg/ml) and analyzed under a fluorescence microscope (Leica Microsystems, Wetzlar, Germany). Negative controls were prepared by omitting incubation in the presence of the enzymatic mixture (data not shown).
Total cell lysates or immunoprecipitated proteins was electrophoresed and transferred to nitrocellulose. Nitrocellulose, blocked in 5% nonfat milk, 10 mmol/l Tris at pH 7.5, 100 mmol/l NaCl, and 0.1% Tween20, was probed with HIF-1α, VEGF, p53, p66Shc, CPP32, and pIkB-α antibodies (Santa Cruz Biotechnology, Santa Cruz, CA) and the incubated in the presence of specific IgG horse-radish peroxidase conjugate. Immunoreactive bands were detected by means of an ECL detection system (Amersham International, Little Chalfont, UK) and analyzed by densitometry.
Quantitative analysis of protein expression was performed by using a Sony video camera connected to a Leica Quantimet 500 plus software (Leica Cambridge Ltd., Cambridge, UK) determining the change in integrated optical intensity (IOI) using ISO transmission density Kodak CAT 152-3406 (Eastman Kodak Company, Rochester, NY) as standard.
Results were expressed as means ± SD of eight different experiments. The values obtained from 12-15 electron micrographs were averaged for any given lung. The mean values were calculated from the morphometric measurements of cell parameters. Statistical comparison between the young group and the corresponding age-matched control group, was performed using an unpaired t-test, with the values of P < 0.01 considered significant (GraphPad Prism Software, Version 5.0). The same analysis was performed for the old group.
Furthermore, in the old rats a substantially increased CPP32 expression was observed (Figure 1 and 2C). VEGF, detected by Western blotting, can be induced in cells that are not receiving enough oxygen. When a cell is deficient in oxygen, it produces HIF which stimulates the release of VEGF among other functions (including modulation of erythropoiesis). The expression of VEGF was also increased in the old rats (Figure 1 and 2C). At the same time there also was a significantly higher expression of pIkB-α in the old rats (Figure 1 and 2B).
Apoptosis is a tightly regulated endogenous cell death program requiring executing proteases. Among the events that determine apoptosis, development, aging, and reduction in oxygen tension are included. During development, apoptosis consists of three types of cell death: phylogenetic, histogenetic, and morphogenetic cell death . During adult and aged life, apoptosis serves to maintain homeostasis by counterbalancing mitosis and deleting vestigial cells which are potentially immunoreactive, malignant, or virus infected. In addition, with age, a progressive decline in cell function can be observed, related either to a genetic program or to accumulation of stochastic errors in somatic cells . However, lipid peroxidation, protein modification, enzyme inactivation, DNA strand breaks, and base modifications are induced, and oxidative damage results [23, 24].
Obviously, the degree to which a pathway is activated depends on the nature and duration of stress as well as on the cell type. Thus, here we tried to match the responses of a rat lung during aging in terms of expression and activation of HIF-1α, p53, p66Shc, CPP32, VEGF, and pIkB-α. Aging and reduced oxygen supply to tissue are two stressful events involved in the induction of HIF-1α expression, activation, and apoptosis . HIF-1α is a key cellular modulator controlled by many different pathways . In the old lungs, HIF-1α expression was not modified compared with young ones. Aging led to increased expression of p53, p66Shc and CPP32 in lungs. These data suggest that apoptosis was in progress. At the same time, the lung tries to counteract apoptosis through the production of VEGF and pIkB-α to adapt itself to a stressful situation and subsequent low availability of oxygen for tissues. The lung may thus attempt to create a life-support system to counteract the apoptotic process and free radical production in the course of the life span.
Conflicts of interest
The authors declare that they have no competing interests.
The first author wish to thank Profs. Camillo Di Giulio, Amelia Cataldi, and Dr. Vittore Verratti for their moral support and unconditional help during the three years of a Ph.D. course.
- Law R, Bukwirwa H: The Physiology of Oxygen Delivery. Update in Anaesthesia 1999, 10: 3.Google Scholar
- Shweiki D, Itin A, Soffer D, Keshet E: Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis. Nature 1992, 359: 843–5. 10.1038/359843a0View ArticlePubMedGoogle Scholar
- Kummer W, Yamamoto Y: Cellular distribution of oxygen sensor candidates-oxidases, cytochromes, K + -channels in the carotid body. Microsc Res Tech 2002, 59: 234–42. 10.1002/jemt.10197View ArticlePubMedGoogle Scholar
- Bianchi G, Di Giulio C, Rapino C, Rapino M, Antonucci A, Cataldi A: p53 and p66 proteins compete for hypoxiainducible factor-1α stabilization in young and old rat hearts exposed to intermittent hypoxia. Gerontology 2006, 52: 17–23. 10.1159/000089821View ArticlePubMedGoogle Scholar
- Ostadal B, Ostadalova I, Dhalla NS: Development of cardiac sensitivity to oxygen deficiency: comparative and ontogenetic aspects. Physiol Rev 1999, 79: 635–59.PubMedGoogle Scholar
- Bunn HF, Poyton RO: Oxygen sensing and molecular adaptation to hypoxia. Physiol Rev 1996, 76: 839–85.PubMedGoogle Scholar
- van den Hoff MJ, van den Eijnde SM, Viragh S, Moor-man AF: Programmed cell death in the developing heart. Cardiovasc Res 2000, 45: 603–20. 10.1016/S0008-6363(99)00401-0View ArticlePubMedGoogle Scholar
- Centurione L, Di Giulio C, Cacchio M, Rapino M, Bosco D, Grifone G, Sabatini N, Bianchi G, Castorina S, Antonucci A, Cataldi A: Correlations between protein kinase C ζ signaling and morphological modifications during rat heart development and aging. Mech Ageing Dev 2003, 124: 957–66. 10.1016/S0047-6374(03)00168-4View ArticlePubMedGoogle Scholar
- Higami Y, Shimokawa I: Apoptosis in the aging process. Cell Tissue Res 2000, 301: 125–32. 10.1007/s004419900156View ArticlePubMedGoogle Scholar
- Cesselli D, Jakoniuk I, Barlucchi L, Beltrami AP, Hintze TH, Nadal-Ginard B, Kajstura J, Leri A, Anversa P: Oxidative stress-mediated cardiac cell death is a major determinant of ventricular dysfunction and failure in dog dilated cardiomyopathy. Circ Res 2001, 89: 279–86. 10.1161/hh1501.094115View ArticlePubMedGoogle Scholar
- Shen Y, White E: p53-dependent apoptosis pathways. Adv Cancer Res 2001, 82: 55–84.View ArticlePubMedGoogle Scholar
- Pan Y, Oprysko PR, Asham AM, Koch CJ, Simon MC: p53 cannot be induced by hypoxia alone but responds to the hypoxic microenvironment. Oncogene 2004, 23: 4975–83. 10.1038/sj.onc.1207657View ArticlePubMedGoogle Scholar
- Suzuki H, Tomida A, Tsuruo T: Dephosphorylated hypoxia-inducible factor 1-alpha as a mediator of p53-dependent apoptosis during hypoxia. Oncogene 2001, 20: 5779–88. 10.1038/sj.onc.1204742View ArticlePubMedGoogle Scholar
- Semenza GL: HIF-1 and mechanisms of hypoxia sensing. Curr Opin Cell Biol 2001, 13: 167–71. 10.1016/S0955-0674(00)00194-0View ArticlePubMedGoogle Scholar
- Trinei M, Berniakovich I, Beltrami E, Migliaccio E, Fassina A, Pelicci P, Giorgio M: p66 Shc signals to age. Aging 2009, 1: 503–10.PubMed CentralPubMedGoogle Scholar
- Woo M, Hakem R, Soengas MS, Duncan GS, Shahinian A, Kägi D, Hakem A, McCurrach M, Khoo W, Kaufman SA, Senaldi G, Howard T, Lowe SW, Mak TW: Essential contribution of caspase 3/CPP32 to apoptosis and its associated nuclear changes. Genes Dev 1998, 12: 806–19. 10.1101/gad.12.6.806PubMed CentralView ArticlePubMedGoogle Scholar
- Moskovitz J, Berlett BS, Poston JM, Stadtman ER: The yeast peptide-methionine sulfoxide reductase functions as an antioxidant in vivo . Proc Natl Acad Sci USA 1997, 94: 9585–9. 10.1073/pnas.94.18.9585PubMed CentralView ArticlePubMedGoogle Scholar
- Migliaccio E, Giorgio M, Mele S, Pelicci G, Reboldi P, Pandolfi PP, Lanfrancone L, Pelicci PG: The p66 Shc adaptor protein controls oxidative stress response and life span in mammals. Nature 1999, 402: 309–13. 10.1038/46311View ArticlePubMedGoogle Scholar
- Abe J, Berk BC: Hypoxia and HIF-1α stability: another stress-sensing mechanism for Shc. Circ Res 2002, 91: 4–6. 10.1161/01.RES.0000026654.65882.55View ArticlePubMedGoogle Scholar
- Piret JP, Mottet D, Raes M, Michiels C: Is HIF-1α a pro-or an anti-apoptotic protein? Biochem Pharmacol 2002, 64: 889–92. 10.1016/S0006-2952(02)01155-3View ArticlePubMedGoogle Scholar
- Jung F, Haendeler J, Hoffmann J, Reissner A, Dernbach E, Zeiher AM, Dimmeler S: Hypoxic induction of the hypoxia-inducible factor is mediated via the adaptor protein Shc in endothelial cells. Circ Res 2002, 91: 38–45. 10.1161/01.RES.0000024412.24491.CAView ArticlePubMedGoogle Scholar
- Camougrand N, Rigoulet M: Aging and oxidative stress: studies of some genes involved both in aging and in response to oxidative stress. Respir Physiol 2001, 128: 393–401. 10.1016/S0034-5687(01)00314-0View ArticlePubMedGoogle Scholar
- Finkel T, Holbrook NJ: Oxidants, oxidative stress and the biology of ageing. Nature 2000, 408: 239–47. 10.1038/35041687View ArticlePubMedGoogle Scholar
- Michiels C, Minet E, Mottet D, Raes M: Regulation of gene expression by oxygen: NF-κB and HIF-1, two extremes. Free Radic Biol Med 2002, 33: 1231–42. 10.1016/S0891-5849(02)01045-6View ArticlePubMedGoogle Scholar
- An WG, Kanekal M, Simon MC, Maltepe E, Blagosklonny MV, Neckers LM: Stabilization of wild-type p53 by hypoxia-inducible factor 1-alpha. Nature 1998, 392: 405–8. 10.1038/32925View ArticlePubMedGoogle Scholar