Cellular senescence increases expression of bacterial ligands in the lungs and is positively correlated with increased susceptibility to pneumococcal pneumonia

doi:10.1111/j.1474-9726.2011.00720.x

Aging Cell. Author manuscript; available in PMC 2012 October 1.

Published in final edited form as:

Aging Cell. 2011 October; 10(5): 798–806.

Published online 2011 June 14. doi: 10.1111/j.1474-9726.2011.00720.x

PMCID: PMC3173515

NIHMSID: NIHMS295929

Cellular senescence increases expression of bacterial ligands in the lungs and is positively correlated with increased susceptibility to pneumococcal pneumonia

Pooja Shivshankar,¹ Angela Rodriguez Boyd,¹ Claude Jourdan Le Saux,² I-Tien Yeh,³ and Carlos J. Orihuela¹

¹ Department of Microbiology and Immunology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, Texas, 78229 USA

² Department of Medicine, Division of Cardiology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, Texas, 78229 USA

³ Department of Pathology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, Texas, 78229 USA

Corresponding Author/Reprints: Carlos Orihuela, PhD, Assistant Professor, Department of Microbiology & Immunology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, Texas 78229-3900, USA, Office phone: (210) 567-3973, Fax: (210) 567-6612, Email: orihuela/at/uthscsa.edu

The publisher's final edited version of this article is available at Aging Cell

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SUMMARY

Cellular senescence is an age-associated phenomenon that promotes tumor invasiveness due to the secretion of pro-inflammatory cytokines, proteases, and growth factors. Herein we demonstrate that cellular senescence also potentially increases susceptibility to bacterial pneumonia caused by Streptococcus pneumoniae (the pneumococcus), the leading cause of infectious death in the elderly. Aged mice had increased lung inflammation as determined by cytokine analysis and histopathology of lung sections. Immunoblotting for p16, pRb, and mH2A showed that elderly humans and aged mice had increased levels of these senescence markers in their lungs versus young controls. Keratin 10 (K10), Laminin Receptor (LR), and Platelet activating factor receptor (PAFr), host proteins known to be co-opted for bacterial adhesion, were also increased. Aged mice were found to be highly susceptible to pneumococcal challenge in a PsrP, the pneumococcal adhesin that binds K10, dependent manner. In vitro senescent A549 lung epithelial cells had elevated K10 and LR protein levels and were up to 5-fold more permissive for bacterial adhesion. Additionally, exposure of normal cells to conditioned media from senescent cells doubled PAFr levels and pneumococcal adherence. Genotoxic stress induced by bleomycin and oxidative stress enhanced susceptibility of young mice to pneumonia and was positively correlated with enhanced p16, inflammation, and LR levels. These findings suggest that cellular senescence facilitates bacterial adhesion to cells in the lungs and provides an additional molecular mechanism for the increased incidence of community-acquired pneumonia in the elderly. This study is the first to suggest a second negative consequence for the senescence-associated secretory phenotype.

Keywords: Cellular senescence, aging, SASP, age-associated inflammation, infectious disease, pneumonia

INTRODUCTION

Pneumonia is the leading cause of infectious death among the elderly (Lopez et al. 2006). Risk factors for community-acquired pneumonia (CAP) include advanced age, underlying morbidities, and the presence of chronic low-grade inflammation (Lexau et al. 2005; Yende et al. 2005). Chronic inflammation is a risk factor for CAP as it results in increased Laminin Receptor (LR) and Platelet-activating Factor receptor (PAFr) protein levels on the surface of host cells (Cundell et al. 1995; Hinojosa et al. 2009; Orihuela et al. 2009). LR and PAFr are in turn co-opted by Streptococcus pneumoniae, Haemophilus influenzae, Neisseria meningitidis and other respiratory tract pathogens for host cell adhesion and bacterial translocation across the alveolar-capillary and blood-brain barriers (Cundell et al. 1995; Swords et al. 2000; Barbier et al. 2008; Orihuela et al. 2009). In support of a strong link between age-associated inflammation and severe pneumonia, it has been previously shown that healthy aged mice express elevated levels of PAFr in their lungs (Hinojosa et al. 2009). Moreover, young mice infused for 5 days with physiologically age-relevant levels of Tumor Necrosis Factor α (TNFα) had elevated levels of lung PAFr and were more susceptible to pneumococcal pneumonia with 100-fold more bacteria in their lungs than saline controls 2 days post-challenge (Hinojosa et al. 2009).

Cellular senescence is an age-associated phenomenon whereby cells with shortened telomeres or those that have undergone DNA damage (i.e. genotoxic stress) lose the capacity to replicate without undergoing apoptosis. This is the result of activation of the p53-p21 and p16-pRb tumor suppressor pathways (Campisi & d’Adda di Fagagna 2007). Cellular senescence has paradoxically been implicated as a tumor-suppressive mechanism due to cell-cycle arrest, as well as a promoter of tumor invasiveness due to the senescence associated secretory phenotype (SASP) which includes the production and secretion of pro-inflammatory cytokines Interleukin (IL)-1α, IL-6 and IL-8, proteases, and assorted growth factors (Coppe et al. 2009). Pertinent to this investigation, proliferation of epithelial cells has also been shown to be modulated by Cytokeratin 10 (K10) (Paramio et al. 1999). During terminal differentiation K10-induced inhibition occurs through pRb as the result of sequestration and phosphorylation of AKT that consequently impedes pRb phosphorylation and leads to cell cycle arrest (Paramio et al. 2001). Coincidently, surface exposed K10 has been demonstrated to serve as a bacterial ligand for the S. pneumoniae adhesin PsrP on lung cells and for the Staphylococcus aureus adhesin ClfB within the nares (O’Brien et al. 2002; Shivshankar et al. 2009).

The presence of senescent cells in the lungs of healthy aged animals has recently been demonstrated by Kreiling et al. using the new senescence marker histone macro H2A (mH2A) (Kreiling et al. 2011). Other investigators have also reported an age-dependent accumulation of senescent cells in skin, liver, atherosclerotic lesions, muscle, and other tissues (Krtolica & Campisi 2002; Campisi 2005; Campisi & d’Adda di Fagagna 2007). Importantly, studies have identified p16 positive senescent cells in the lungs of individuals with chronic obstructive pulmonary disease (COPD) and they are thought to exacerbate pathology due to their pro-inflammatory phenotype (Garcia et al. 2007; Aoshiba & Nagai 2009; Tsuji et al. 2010). Both COPD and advanced age are established risk factors for CAP (Lexau et al. 2005).

Given the documented presence of senescent cells in aged tissues, the pro-inflammatory phenotype of senescent cells, and the fact that inflammation is a risk factor for CAP due to increased ligand expression in the lungs, we hypothesized that cellular senescence enhances susceptibility to pneumococcal pneumonia through increased bacterial ligand expression. In the present study we therefore tested young and aged mice for levels of senescence markers in their lungs, assessed whether senescent lung cells expressed elevated levels of the pneumococcal ligands K10, LR, and PAFr in vitro and in vivo, tested for a paracrine effect of SASP on bacterial adhesion, and determined whether genotoxic stress increased susceptibility to pneumococcal infection.

RESULTS

Age-associated inflammation occurs in the lungs of healthy aged animals and is positively correlated with increased levels of senescence markers

Consistent with the concept of age-associated inflammation, lung homogenates from healthy aged (19–22 month) mice had increased levels of the pro-inflammatory cytokines IL-1α, IL-1β, IL-6, TNFα, and CXCL1 versus those obtained from young (4–5 month) animals (Figure 1A). Likewise, histological examination of lung sections from the same animals showed that aged mice had an increased incidence of interstitial and peribronchial inflammation (Figure 1B,C). In agreement with findings by Kreiling et al. showing that senescent cells are present in the lungs of healthy aged C57Bl/6 mice (Kreiling et al. 2011), in both human and Balb/cBy mouse lung samples, we observed an age-dependent increase in the senescence markers p16 and pRb by Western blot (Figure 2). For mature (51–63 year) and aged (64–82 year) humans we also observed increased levels of mH2A versus younger controls (43–50 year). Thus the pro-inflammatory cytokine profile observed in healthy aged mice was correlated positively with elevated p16 and pRb levels. These findings support the concept that cellular senescence occurs in the aged lungs and acts as a source of inflammation.

Figure 1

Aged mice experience low-grade lung inflammation

Figure 2

Aging is associated with increased expression of senescence markers in the lungs

Pneumococcal ligands are elevated in aged lungs and contribute to the enhanced susceptibility to pneumonia

As indicated S. pneumoniae binds to the host-proteins K10, LR, and PAFr on lung cells (Cundell et al. 1995; Orihuela et al. 2009; Shivshankar et al. 2009). Western blot analyses of whole lung homogenates from young, mature, and aged human lung biopsy samples demonstrated an age dependent increase in LR and PAFr, with a trend for K10 in young versus aged samples (P=0.17) (Figure 3A). Aged mice showed a statistically significant increase in all three ligands versus young controls (Figure 3B). Immunohistochemistry of mouse lung sections confirmed these observations for K10 with intense staining for both the alveolar and bronchial epithelial cells but not endothelial cells or fibroblasts surrounding the bronchi of aged mice versus young controls (Figure 3C).

Figure 3

Aging is associated with increased bacterial ligand expression in the lungs

An important role for elevated K10 during pneumococcal pneumonia in aged mice was confirmed by challenging young and aged animals with wild type bacteria or with an isogenic mutant deficient in PsrP (ΔpsrP) (Rose et al. 2008). Not only was mortality in aged mice PsrP-dependent (Figure 4A), but two days after challenge aged mice infected with the wild type strain had median bacterial titers in their lungs and blood 10- and 240-fold greater, respectively, than those infected with the mutant strain (Figure 4B). Thus we determined that increased K10, LR, and PAFr expression occurred in the lungs of aged humans and mice. Furthermore, aged mice were more susceptible to pneumococcal infection in a PsrP/K10 dependent manner.

Figure 4

Aging enhances susceptibility to pneumococcal pneumonia in a K10-dependent manner

Senescent lung epithelial cells express K10 and LR

We subsequently tested whether induction of cellular senescence resulted in elevated K10, LR, and PAFr production by lung epithelial cells. In vitro treatment of A549 human type II pneumocytes with bleomycin resulted in cellular senescence. Indeed, we observed the expected phenotypic changes such as cell flattening, increased senescence-associated β-galactosidase activity, and elevated expression of p16, pRb, and mH2A along with a decline in phospho-pRb by immunoblotting (Figure 5A,B). Induction of senescence with bleomycin resulted in a dose-dependent increase in the expression of K10 and LR, but not PAFr (Fig 5B). Subsequently, immunofluorescence assay confirmed nuclear accumulation of pRb simultaneous to increased K10 expression in bleomycin treated cells but not in controls (Figure 5C). Finally, bacterial adhesion assays demonstrated that senescent cells were more permissive for infection with a 3 to 5-fold increase in the number of attached wild type but not PsrP-deficient pneumococci to senescent cells when compared to normal cells (Figure 5D,E). Thus induction of cellular senescence in lung cells was associated with increased expression of two pneumococcal ligands and increased permissiveness for bacterial attachment.

Figure 5

Senescent lung cells express enhanced levels of pneumococcal ligands and are permissive for bacterial adhesion in vitro

SASP enhances permissiveness of normal cells for infection

PAFr and LR have been shown to be upregulated by lung cells following exposure to pro-inflammatory cytokines (Cundell et al. 1995; Orihuela et al. 2009). Thus it is possible that SASP enhances bacterial ligand expression on pre-senescent normal lung cells in a paracrine manner. In vitro, we confirmed that bleomycin-induced senescent A549 cells increased intracellular IL-1α levels but that it was not secreted (Figure 6A). Further, senescent cells secreted increased amounts of IL-6 and IL-8 but did not produce IL-1β, TNFα, IL-10 or IL-12 (Figure 6A). Normal A549 cells exposed to conditioned-media from senescent cells for 2 hours presented a 2.2-fold increase in bacterial adhesion compared to cells exposed to conditioned media from normal cells (Figure 6B). Finally, treatment of A549 cells with senescent media resulted in no changes in K10 or LR, but resulted in a doubling of PAFr levels after 2 hours (Figure 6C). The latter remained constant through 4 and 6 hours of incubation with conditioned media (data not shown).

Figure 6

Normal A549 cells exposed to conditioned media from senescent cells are permissive for bacterial adhesion

Genotoxic stress enhances susceptibility of young mice to pneumonia

Finally, we tested whether administration of agents known to cause DNA damage enhanced bacterial ligand expression and susceptibility to pneumonia. Genotoxic stress in young mice was induced either by intratracheal administration of bleomycin once (0.033 mg/kg body weight) or supplementation of drinking water with 0.5% hydrogen peroxide for 3 weeks. The latter causes DNA damage through oxidative stress (Weiner et al. 2000). In mice administered bleomycin and hydrogen peroxide we observed dramatic changes in lung histology and high levels of IL-1α, IL-1β, IL-6, CXCL1, and TNFα (Supplementary Figure 1). Both bleomycin and hydrogen peroxide treated mice were highly susceptible to pneumococcal infection versus saline administered controls. Two days post-challenge, bleomycin- and hydrogen peroxide-treated mice had 10 to 100-fold more bacteria in their lungs and bloodstream than their respective controls (Figure 7A). Levels of p16, pRb, and LR were elevated in the lungs of genotoxic stressed mice, whereas mH2A, K10, and PAFr were unchanged (Figure 6B). Thus administration of genotoxic agents had pleiotropic effects that included significant changes in lung structure along with increased expression of senescence markers and susceptibility to bacterial infection.

Figure 7

Genotoxic stress enhances susceptibility to pneumonia and is positively correlated with increased bacterial ligand expression

DISCUSSION

Advanced age is an established risk factor for CAP (Lexau et al. 2005), with more than 800 million people worldwide greater than 65 years of age (Kinsella & Velkoff 2001). Overlapping with this, 210 million adults have COPD worldwide (WHO 2009), a condition associated with and exacerbated by cellular senescence that is also a risk factor for CAP (Lexau et al. 2005; Aoshiba & Nagai 2009). Thus, close to 1 billion adults worldwide are at risk for pneumonia. Our finding that senescent lung cells have increased levels of K10 and LR, and can induce the expression of PAFr on normal cells, potentially helps to explain why the elderly and individuals with COPD are predisposed for CAP. Specifically we have demonstrated that senescent cells, normal cells exposed to senescent-conditioned media, aged mice, and young mice exposed to genotoxic stress, were more permissive for bacterial adhesion and susceptible to pneumococcal pneumonia, respectively.

The age-associated increase in inflammation that we observed in the lungs of healthy aged mice was consistent with prior publications that have shown elevated levels of IL-6, IL-8, and neutrophils within the lungs of healthy elderly human volunteers (Meyer et al. 1996; Meyer et al. 1998). Likewise, they were consistent with the reported SASP profile for senescent HeLa cells (Coppe et al. 2008), and that observed herein for senescent lung epithelial cells. Our observation that elderly humans and aged mice had enhanced levels of p16 and pRb were also in agreement with those by others demonstrating elevated levels of senescent cells in the lungs of aged mice and elevated senescence markers in multiple tissues from aged animals (Campisi 2005; Kreiling et al. 2011). Thus considerable evidence now exists that cellular senescence occurs in the aged lungs and that it contributes to the observed age-associated inflammation. Notably, although increased for humans, levels of mH2A were not increased in the lungs of 19–22 month (i.e. aged) Balb/cBy mice when examined by Western blot. This was in contrast to that observed by Kreiling et al. in C57Bl/6 mice but may be due to the fact that they examined 36-month old animals (Kreiling et al. 2011).

Bacterial attachment to lung cells is a requisite event in the pathogenesis of pneumonia (Kline et al. 2009; Paterson & Orihuela 2010). This is particularly true for the encapsulated extracellular respiratory tract pathogens such as S. pneumoniae (Orihuela et al. 2005). Yende et al. and our own studies have shown elevated levels of IL-6 and TNFα are risk factors for CAP as a result of enhanced bacterial ligand expression (Yende et al. 2005; Hinojosa et al. 2009). PAFr serves as a ligand for S. pneumoniae, Haemophilus influenzae, and Pseudomonas aeruginosa as well as many other bacteria that have surface exposed phosphorylcholine on their surface (Cundell et al. 1995; Swords et al. 2000; Barbier et al. 2008). LR serves as a ligand for H. influenzae and Neisseria meningitidis (Orihuela et al. 2009). K10 is also a ligand for PsrP from S. pneumoniae and ClfB of Staphylococcus aureus (O’Brien et al. 2002; Shivshankar et al. 2009). Respiratory tract pathogens also bind to other inflammation-regulated proteins such as Inter-cellular adhesion molecule 1 (ICAM-1) and Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) that were not tested but are also most likely up-regulated as a result of age-associated inflammation (Avadhanula et al. 2006; Conners et al. 2008). Thus the enhanced expression of bacterial ligands on either senescent cells or normal cells exposed to SASP is one mechanism by which the lungs of the elderly and COPD patients may be primed for infection by numerous pathogens.

Between young and aged mice and in humans, the most dramatic difference in ligand levels that we observed was in regards to K10. Increased survival of aged mice infected with a PsrP-deficient mutant demonstrated the importance of this host-ligand interaction for severe pneumococcal disease. Unlike LR or PAFr, which are ubiquitously expressed, K10 is found predominantly in differentiated keratinocytes and on mucosal epithelial cells of the lungs and nares (Paramio et al. 2001; O’Brien et al. 2002; Shivshankar et al. 2009). Thus the contribution of elevated K10 to infection is most likely limited to the lungs and not during sepsis or meningitis. Of note, passive and active immunization with PsrP has been shown to be protective against challenge in young mice (Rose et al. 2008; Shivshankar et al. 2009). This indicates that vaccines designed for use in the elderly might be optimized to neutralize the activity of bacterial adhesins that target age-dependent inflammation-regulated ligands on host cells, such as K10.

We observed that induction of senescence with bleomycin enhanced K10 expression in alveolar epithelial cells in vitro. Because K10 expression has been shown to result in pRb activation and cell cycle arrest (Paramio et al. 1999; Paramio et al. 2001), this observation suggests that K10 may be involved in a positive-feed back loop with pRb that together leads to epithelial cell senescence. Further studies are warranted to examine this possibility. Induction of genotoxic stress with H₂O₂ and bleomycin corroborated the role of cellular senescence in susceptibility of live animals to infection, but was obfuscated by the pleiotropic effects of these genotoxic agents. Although administration of H₂O₂ results in generalized oxidative stress and bleomycin causes lung fibrosis, exposure to non-specific genotoxic stress occurs during smoking and possibly explains the high incidence of cellular senescence in the lungs of individuals with COPD (Aoshiba et al. 2003; Aoshiba & Nagai 2009).

At this time, it not possible to block the development of cellular senescence in aged mice. Thus a direct cause and effect relationship between senescent cells and the susceptibility of aged animals to pneumonia could not be demonstrated. While multiple factors were potentially involved in the increased susceptibility of aged mice to pneumonia, our observation of increased expression of p16, pRb and mH2A, enhanced lung inflammation, increased bacterial attachment to senescent cells and normal cells exposed to senescent media, and the enhanced susceptibility of aged mice to infection in a PsrP-dependent manner are strong correlative findings that support the hypothesis that senescent cells prime the lungs for pneumonia through increased bacterial adhesion. These findings clearly suggest that cellular senescence impacts inflammation and infectious disease in the lungs and provide an additional molecular explanation for the increased incidence of CAP in the elderly and those with COPD.

EXPERIMENTAL PROCEDURES

All animal experiments and those with de-identified human tissues and were reviewed and approved by the appropriate University of Texas Health Science Center institutional review board.

Collection and processing of lung samples

Young (4 to 5 months) and aged (19–22 months) female Balb/cBy mice were obtained from the National Institute on Aging Aged Rodent Colony and housed in ABSL-1 facilities. Following their asphyxiation with isoflurane, lungs were excised, washed with sterile phosphate buffered saline (PBS), and processed for paraffin embedding and collection of whole lung homogenates. Human lung samples were obtained from the Lung Tissue Research Consortium (LTRC) sponsored by National Heart, Lung and Blood Institute. Frozen tissue blocks were obtained from young (43–50 years), mature (51–64 years), and elderly (65–82 years) individuals during lung biopsy sample collection or surgical resection. Only normal tissues, as determined by pathological examination by LTRC staff were used. Paraffin-embedded lungs were sectioned at 5 μm thickness and stained with hematoxylin and eosin for pathological examination. Five lung sections from each mouse were scored on a 1–5 scale on the basis of peribronchial, perivascular, and intraalveolar inflammation, interstitial pneumonitis, and thickening of the alveolar walls. Unstained sections were utilized for immunohistochemical analyses as described below.

Analysis of pro-inflammatory cytokine production

Cytokine levels in tissue homogenates were determined by ELISA using IL-1α, IL-1β, IL-6, TNFα and CXCL1 kits from BD Pharmingen. Levels of IL-1β, IL-6, IL-8, IL-10, IL-12p70 and TNFα in A549 cell supernatants were determined using a BDCytometric Bead Array (CBA) Human Inflammatory Cytokines Kit. Levels of IL-1α produced by these cells were determined using a human IL-1α ELISA kit (R&D).

Immunoblotting

Whole lung homogenates and A549 cell lysates were prepared in appropriate volumes of RIPA buffer and the protein concentration determined using the bicinchoninic acid assay. Immunoblotting was carried out with 10–15 μg protein per sample using standard protocols. Primary antibodies used included rabbit anti-human K10 (Epitomics), mouse anti-human LR (Abcam), rabbit anti-human PAFr (Cayman Chemicals), rabbit anti-human actin (Abcam), mouse anti-human pRb (Cell Signaling), rabbit anti-mouse pRb (Cell Signaling), rabbit anti-phospho-pRb (Cell Signaling), rabbit anti-human p16 (Santa Cruz), and rabbit anti-histone mH2A1 (Millipore). Primary antibodies were shown by the manufacturer to cross react with both mouse and human orthologues except for pRb. All antibodies were used at a minimal dilution of 1:500.

Semi-quantitative analyses of immunoblots

Relative protein levels were determined by comparative densitometric analysis of Western blot bands using a Molecular Imager Gel Doc XR System (BioRad, Hercules, CA). For each protein examined, the membrane initially probed was stripped and the amount of actin determined using rabbit anti-actin antibodies (Bethyl laboratories, Inc., Montgomery, TX). Relative levels of protein were determined by dividing the intensity of the tested protein band to that of actin within the same lane and membrane.

Immunohistochemistry for K10

Paraffin-embedded lung sections were deparaffinized with xylene and rehydrated using an ethanol gradient. Following rinsing with PBS, the sections were treated with 0.3% H₂O₂ in 100% methanol to quench endogenous peroxidase activity. Slides were rinsed twice with PBS then submerged in 4% paraformaldehyde for 20 min at room temperature. Sections were washed twice with PBS then microwaved twice in Target Unmasking Fluid (Invitrogen) for 5 min with a 1-minute interval. After cooling in room temperature water, tissue sections were blocked with 10% FBS in PBS for 1 hour at room temperature. The sections were then incubated with antibody against K10 (1:40) at 4° C overnight. Sections were washed thrice with PBS and incubated with goat anti-rabbit IgG conjugated to HRP (1:200 dilution) for 1 hour at room temperature. The slides were washed four times then stained with the DAB substrate kit following the manufacturer’s protocol (BD Parmingen). Following color development, slides were rinsed with water then counterstained for 2 minutes with hematoxylin. Sections were dehydrated and cover slipped using standard protocols. For each mouse (n=5 per age group) 2 lung sections were examined using a light microscope at a magnification of 400X. Images were captured and processed using Leica software.

Infection of mice with S. pneumoniae

S. pneumoniae, serotype 4 strain TIGR4 and T4ΔpsrP, a previously described isogenic mutant deficient in psrP, were grown on blood agar plates or in Todd Hewitt broth (THB) at 37° C in 5% CO₂ (Obert et al. 2006; Rose et al. 2008). Erythromycin (1 μg/ml) was added to the culture media to maintain the psrP mutation. Bacterial cultures were grown to mid-logarithmic phase (OD₆₂₀ = 0.5), pelleted by centrifugation, and suspended in sterile PBS. For assessment of the contribution of PsrP/K10 to age-dependent disease severity mice were infected intranasally with 10⁷ and 10⁶ CFU of TIGR4 or T4ΔpsrP in a 25μl suspension. Mortality over 10 days was assessed. To determine age-related changes in bacterial titers, a parallel set of mice were inoculated intratracheally with 10⁵ CFU in 100μl PBS. Two days post-challenge mice were sacrificed and the lungs and blood collected. Bacterial titers in the lungs and blood were determined by plating serial dilutions of the lung homogenate or blood and extrapolation from colony counts following overnight incubation. All animal infection studies were conducted in ABSL-2 facilities.

Induction of cellular senescence in vitro

A549 (ATCC CRL-185) cells were maintained in F12 medium supplemented with 10% fetal bovine serum and antibiotics. A549 cells were pulsed with 0–25 μg/ml bleomycin sulfate for 1 day then washed and maintained in fresh culture medium for 8 days. Cellular senescence was confirmed by the detection of senescence associated β-galactosidase activity (Dimri et al. 1995; Debacq-Chainiaux et al. 2009).

Immunofluorescence assay

Detection of pRb and K10 was carried out as described previously (Shivshankar et al. 2009) with brief modifications. Eight days after control or bleomycin-pulse A549 cells grown on coverslips were washed and fixed in 4% paraformaldehyde for 20 minutes at room temperature. Cells were permeabilized with 0.1% triton-X-100 for 5 minutes and blocked in 10% FBS-containing F12 medium for 1 hour at room temperature. Primary antibodies for pRb (mouse anti-human pRb) and K10 (rabbit anti-human K10) were added at 1:100 dilution and incubated at 4° C overnight. Cells were washed with PBS thrice for 5 minutes and incubated with goat anti-mouse IgG PE and goat anti-rabbit FITC (1:200 dilution) to detect pRb and K10, respectively, along with DAPI for nuclear staining for 1 hour at room temperature. Cells were washed and coverslips mounted on glass slides using Fluorsave mounting solution (Merckbio). Fluorescent staining in the cells was observed using Olympus AX-70 Fluorescence microscope, and images were acquired using a Hamamatsu digital camera. All single-color images were then superimposed and processed with the software SimplePCI to display multicolors.

Adhesion assays

Bacterial adhesion assays were performed using protocols previously described (Rose et al. 2008; Shivshankar et al. 2009). Exponential cultures of S. pneumoniae were pelleted and suspended in PBS at 10⁷ CFU/ml (OD₆₂₀ = 0.1) and added to confluent monolayers of control and bleomycin-pulsed A549 in a 24 well plate (2.0 cm²). After 1 hour incubation at 37° C, cells were washed gently with PBS thrice to remove unattached bacteria, lysed with 0.1% Triton-X-100 in PBS, and the lysate plated on blood agar plates and incubated for extrapolation of attached bacteria from the number of colonies. Transiently transfected A549 cells with pCDNA-K10 were used as positive controls to compare the effect of bleomycin on pneumococcal adhesion (Paramio et al. 1999; Shivshankar et al. 2009). Adhesion assays were done at minimum in triplicate with 3 wells per condition tested in each experiment. Due to the difference in cell size between normal and senescent cells, bacterial adhesion data is presented as the percent adhesion relative to WT-infected untreated cell monolayers (i.e. equal surface area), likewise, as the number of attached bacteria per 100,000 A549 cells. To determine the latter, monolayers were trypsinized and cells counted using a Neubauer hemocytometer. For analysis of the paracrine effect of senescent cells on adhesion cell culture supernatants from control and bleomycin-treated A549 cells after 8 days were applied to fresh monolayer of A549 cells for 2 hours prior to the addition of bacteria.

Induction of genotoxic stress

Bleomycin sulfate at 0.033 mg/Kg body weight was administered intratracheally to 4–5 month old female Balb/cJ following the protocol described by Aoshiba et al. (Aoshiba et al. 2003). Control animals were administered sterile PBS, which was used as the bleomycin vehicle. Three weeks later mice were used for experimental purposes. Alternatively, oxidative stress was induced using the protocol previously described by Weiner et al. (Weiner et al. 2000). Briefly, mice were given drinking water supplemented with 0.5% H₂O₂ ad libitum for 3 weeks prior to their experimental use.

Statistical analysis

For statistical comparisons between 2 cohorts a two-tailed Student’s t-test was used. For the comparison of bacterial burden between young and aged mice challenged with wild type and mutant S. pneumoniae, a One-Way ANOVA (Duncan’s test) was used. For analysis of survival following bacteria challenge a Kaplan- Meier Log Rank test was employed. All statistical analyses were performed using SigmaStat software (Systat Software).

Supplementary Material

Supp Fig S1

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Acknowledgments

Role of funding source: The funding sources had no involvement in study design, in the collection, analysis, and interpretation of the data, or in the writing of the report.

We thank Benjamin J. Daniel for assistance with cytometric analyses. For CJLS this work was supported by the Leahi Foundation. For CJO this work was supported by the National Institute for Health grants AG092313, AG033274 and AI078972.

Footnotes

CONFLICT OF INTETEREST

None of the authors have a conflict of interest.

References

Aoshiba K, Nagai A. Senescence hypothesis for the pathogenetic mechanism of chronic obstructive pulmonary disease. Proc Am Thorac Soc. 2009;6:596–601. [PubMed]
Aoshiba K, Tsuji T, Nagai A. Bleomycin induces cellular senescence in alveolar epithelial cells. Eur Respir J. 2003;22:436–443. [PubMed]
Avadhanula V, Rodriguez CA, Ulett GC, Bakaletz LO, Adderson EE. Nontypeable Haemophilus influenzae adheres to intercellular adhesion molecule 1 (ICAM-1) on respiratory epithelial cells and upregulates ICAM-1 expression. Infection and immunity. 2006;74:830–838. [PMC free article] [PubMed]
Barbier M, Oliver A, Rao J, Hanna SL, Goldberg JB, Alberti S. Novel phosphorylcholine-containing protein of Pseudomonas aeruginosa chronic infection isolates interacts with airway epithelial cells. J Infect Dis. 2008;197:465–473. [PubMed]
Campisi J. Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors. Cell. 2005;120:513–522. [PubMed]
Campisi J, d’Adda di Fagagna F. Cellular senescence: when bad things happen to good cells. Nat Rev Mol Cell Biol. 2007;8:729–740. [PubMed]
Conners R, Hill DJ, Borodina E, Agnew C, Daniell SJ, Burton NM, Sessions RB, Clarke AR, Catto LE, Lammie D, Wess T, Brady RL, Virji M. The Moraxella adhesin UspA1 binds to its human CEACAM1 receptor by a deformable trimeric coiled-coil. Embo J. 2008;27:1779–1789. [PMC free article] [PubMed]
Coppe JP, Desprez PY, Krtolica A, Campisi J. The senescence-associated secretory phenotype: the dark side of tumor suppression. Annu Rev Pathol. 2009;5:99–118. [PubMed]
Coppe JP, Patil CK, Rodier F, Sun Y, Munoz DP, Goldstein J, Nelson PS, Desprez PY, Campisi J. Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor. PLoS Biol. 2008;6:2853–2868. [PMC free article] [PubMed]
Cundell DR, Gerard NP, Gerard C, Idanpaan-Heikkila I, Tuomanen EI. Streptococcus pneumoniae anchor to activated human cells by the receptor for platelet-activating factor. Nature. 1995;377:435–438. [PubMed]
Debacq-Chainiaux F, Erusalimsky JD, Campisi J, Toussaint O. Protocols to detect senescence-associated beta-galactosidase (SA-betagal) activity, a biomarker of senescent cells in culture and in vivo. Nat Protoc. 2009;4:1798–1806. [PubMed]
Dimri GP, Lee X, Basile G, Acosta M, Scott G, Roskelley C, Medrano EE, Linskens M, Rubelj I, Pereira-Smith O, et al. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. Proc Natl Acad Sci U S A. 1995;92:9363–9367. [PubMed]
Garcia CK, Wright WE, Shay JW. Human diseases of telomerase dysfunction: insights into tissue aging. Nucleic Acids Res. 2007;35:7406–7416. [PMC free article] [PubMed]
Hinojosa E, Boyd AR, Orihuela CJ. Age-associated inflammation and toll-like receptor dysfunction prime the lungs for pneumococcal pneumonia. J Infect Dis. 2009;200:546–554. [PMC free article] [PubMed]
Kinsella K, Velkoff VA. USC Bureau. An Aging World: 2001. Washington D.C.: U.S. Goverment Printing Office; 2001.
Kline KA, Falker S, Dahlberg S, Normark S, Henriques-Normark B. Bacterial adhesins in host-microbe interactions. Cell Host Microbe. 2009;5:580–592. [PubMed]
Kreiling JA, Tamamori-Adachi M, Sexton AN, Jeyapalan JC, Munoz-Najar U, Peterson AL, Manivannan J, Rogers ES, Pchelintsev NA, Adams PD, Sedivy JM. Age-associated increase in heterochromatic marks in murine and primate tissues. Aging Cell. 2011;10:292–304. [PMC free article] [PubMed]
Krtolica A, Campisi J. Cancer and aging: a model for the cancer promoting effects of the aging stroma. The International Journal of Biochemistry & Cell Biology. 2002;34:1401–1414. [PubMed]
Lexau CA, Lynfield R, Danila R, Pilishvili T, Facklam R, Farley MM, Harrison LH, Schaffner W, Reingold A, Bennett NM, Hadler J, Cieslak PR, Whitney CG. Changing epidemiology of invasive pneumococcal disease among older adults in the era of pediatric pneumococcal conjugate vaccine. JAMA. 2005;294:2043–2051. [PubMed]
Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJ. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet. 2006;367:1747–1757. [PubMed]
Meyer KC, Ershler W, Rosenthal NS, Lu XG, Peterson K. Immune dysregulation in the aging human lung. Am J Respir Crit Care Med. 1996;153:1072–1079. [PubMed]
Meyer KC, Rosenthal NS, Soergel P, Peterson K. Neutrophils and low-grade inflammation in the seemingly normal aging human lung. Mech Ageing Dev. 1998;104:169–181. [PubMed]
O’Brien LM, Walsh EJ, Massey RC, Peacock SJ, Foster TJ. Staphylococcus aureus clumping factor B (ClfB) promotes adherence to human type I cytokeratin 10: implications for nasal colonization. Cell Microbiol. 2002;4:759–770. [PubMed]
Obert C, Sublett J, Kaushal D, Hinojosa E, Barton T, Tuomanen EI, Orihuela CJ. Identification of a candidate Streptococcus pneumoniae core genome and regions of diversity correlated with invasive pneumococcal disease. Infect Immun. 2006;74:4766–4777. [PMC free article] [PubMed]
Orihuela CJ, Fogg G, DiRita VJ, Tuomanen E. Bacterial interactions with mucosal epithelial cells. In: Mestecky J, Lamm ME, Strober W, Bienenstock J, McGhee JR, Mayer L, editors. Mucosal Immunology. Burlington, MA: Elsevier Academic Press; 2005. pp. 753–767.
Orihuela CJ, Mahdavi J, Thornton J, Mann B, Wooldridge KG, Abouseada N, Oldfield NJ, Self T, Ala’Aldeen DA, Tuomanen EI. Laminin receptor initiates bacterial contact with the blood brain barrier in experimental meningitis models. J Clin Invest. 2009;119:1638–1646. [PMC free article] [PubMed]
Paramio JM, Casanova ML, Segrelles C, Mittnacht S, Lane EB, Jorcano JL. Modulation of cell proliferation by cytokeratins K10 and K16. Mol Cell Biol. 1999;19:3086–3094. [PMC free article] [PubMed]
Paramio JM, Segrelles C, Ruiz S, Jorcano JL. Inhibition of protein kinase B (PKB) and PKCzeta mediates keratin K10-induced cell cycle arrest. Mol Cell Biol. 2001;21:7449–7459. [PMC free article] [PubMed]
Paterson GK, Orihuela CJ. Pneumococcal microbial surface components recognizing adhesive matrix molecules targeting of the extracellular matrix. Mol Microbiol. 2010;77:1–5. [PMC free article] [PubMed]
Rose L, Shivshankar P, Hinojosa E, Rodriguez A, Sanchez CJ, Orihuela CJ. Antibodies against PsrP, a novel Streptococcus pneumoniae adhesin, block adhesion and protect mice against pneumococcal challenge. J Infect Dis. 2008;198:375–383. [PubMed]
Shivshankar P, Sanchez C, Rose LF, Orihuela CJ. The Streptococcus pneumoniae adhesin PsrP binds to Keratin 10 on lung cells. Mol Microbiol. 2009;73:663–679. [PMC free article] [PubMed]
Swords WE, Buscher BA, Ver Steeg Ii K, Preston A, Nichols WA, Weiser JN, Gibson BW, Apicella MA. Non-typeable Haemophilus influenzae adhere to and invade human bronchial epithelial cells via an interaction of lipooligosaccharide with the PAF receptor. Mol Microbiol. 2000;37:13–27. [PubMed]
Tsuji T, Aoshiba K, Nagai A. Alveolar cell senescence exacerbates pulmonary inflammation in patients with chronic obstructive pulmonary disease. Respiration. 2010;80:59–70. [PubMed]
Weiner ML, Freeman C, Trochimowicz H, de Gerlache J, Jacobi S, Malinverno G, Mayr W, Regnier JF. 13-week drinking water toxicity study of hydrogen peroxide with 6-week recovery period in catalase-deficient mice. Food Chem Toxicol. 2000;38:607–615. [PubMed]
WHO; WM centre. Chronic obstructive pulmonary disease (COPD) World Health Organization; 2009.
Yende S, Tuomanen EI, Wunderink R, Kanaya A, Newman AB, Harris T, de Rekeneire N, Kritchevsky SB. Preinfection systemic inflammatory markers and risk of hospitalization due to pneumonia. Am J Respir Crit Care Med. 2005;172:1440–1446. [PMC free article] [PubMed]