American Journal of Respiratory and Critical Care Medicine

Rationale: Bombesin-like peptides promote fetal lung development. Normally, levels of mammalian bombesin (gastrin-releasing peptide [GRP]) drop postnatally, but these levels are elevated in newborns that develop bronchopulmonary dysplasia (BPD), a chronic lung disease characterized by arrested alveolarization. In premature baboons with BPD, antibombesin antibodies reduce lung injury and promote alveolarization.

Objectives: The present study tests whether exogenous bombesin or GRP given perinatally alters alveolar development in newborn mice.

Methods: Mice were given peptides intraperitoneally twice daily on Postnatal Days 1–3. On Day 14 lungs were inflation-fixed for histopathologic analyses of alveolarization.

Measurements and Main Results: Bombesin had multiple effects on Day 14 lung, when alveolarization was about half complete. First, bombesin induced alveolar myofibroblast proliferation and increased alveolar wall thickness compared with saline-treated control animals. Second, bombesin diminished alveolarization in C57BL/6 (but not Swiss-Webster) mice. We used receptor-null mice to explore which receptors might mediate these effects. Compared with wild-type littermates, bombesin-treated GRP receptor (GRPR)–null mice had increased interstitial fibrosis but reduced defects in alveolarization. Neuromedin B (NMB) receptor–null and bombesin receptor subtype 3–null mice had the same responses as their wild-type littermates. GRP had the same effects as bombesin, whereas neither NMB nor a synthetic bombesin receptor type 3 ligand had any effect. All effects of GRP were abrogated in GRPR-null mice.

Conclusions: Bombesin/GRP can induce features of BPD, including interstitial fibrosis and diminished alveolarization. GRPR appears to mediate all effects of GRP, but only part of the bombesin effect on alveolarization, suggesting that novel receptors may mediate some effects of bombesin in newborn lung.

Bombesin is a 14–amino acid peptide originally identified in 1971 by Erspamer in skin of the frog Bombina bombina (13). Using antibodies to amphibian bombesin, a 27–amino acid mammalian homolog was identified by McDonald and termed gastrin-releasing peptide (GRP) (4). GRP and bombesin share a highly conserved seven–amino acid C-terminus, which is required for immunogenicity and high-affinity binding to physiologic receptors. Thus, bombesin and GRP are referred to collectively as “bombesin-like peptides” (BLPs), because both peptides bind to and elicit the same physiologic effects at mammalian bombesin/GRP-preferring receptors. BLP immunoreactivity is widely distributed in the central nervous system, the lung, and the gut, but the highest levels occur in mid-gestation human fetal lung (2, 5).

During lung development, the first epithelial cells to differentiate are the pulmonary neuroendocrine cells (6, 7), which contain high levels of BLP immunoreactivity. BLP can promote growth and maturation of developing fetal lung in humans, nonhuman primates, rats, and mice (810). Levels of GRP receptor (GRPR) and GRP mRNAs peak during the canalicular phase, then fall to much lower levels during normal alveolarization after birth (8, 11).

Bronchopulmonary dysplasia (BPD), also known as chronic lung disease of newborns, is the most prevalent of the long-term sequelae that affect surviving preterm infants. The pathophysiology of BPD is multifactorial, with contributing factors including barotrauma, oxygen toxicity, and pulmonary immaturity (12, 13). Increased numbers of BLP-positive pulmonary neuroendocrine cells have been observed in infants dying with BPD (14). Elevated urine BLP during the first week after birth is a strong risk factor for premature human infants, associated with a 10-fold increased risk of developing BPD, occurring shortly after birth in a majority of premature human infants who later develop BPD (15). Similarly, elevated urine BLP levels occur in premature newborns from two different baboon models of BPD (16). As a potent growth factor for normal bronchial epithelial cells and embryonic fibroblasts, and a direct bronchoconstrictor, BLP could promote peribronchiolar fibrosis, obliterative bronchiolitis, and reactive airways disease, which are characteristic of BPD (2, 3, 17, 18). Consistent with this hypothesis, the blocking anti-BLP antibody 2A11 given postnatally abrogates clinical and pathologic parameters of lung injury in baboons at risk for BPD (16).

The present study addresses two novel hypotheses: first, that BLP given to developing mouse pups can directly induce histopathologic features of BPD; and second, that these changes are mediated by one or more mammalian BLP receptors. The three cloned mammalian bombesin receptor subtypes have distinct distributions in the central nervous system and peripheral organs (19), suggesting that they may transduce different biological effects. These heptahelical G protein–coupled receptors are: GRPR (20), neuromedin B receptor (NMBR) (21), and the orphan bombesin receptor subtype 3 (BRS3) (22). GRPR-null mice manifest increased locomotor activity, whereas analyses of NMBR-null mice support a role for NMBR in thermoregulation (20, 21). Finally, mice lacking BRS3 develop hyperphagia, obesity with associated hypertension, reduced metabolic rate, and impaired glucose metabolism (22).

It is known that both GRP and bombesin bind to the same high-affinity bombesin/GRP–preferring receptor, leading to essentially identical effects in mammalian systems, which is due to their shared bioactive amidated carboxy terminal sequence (2). In fact, amphibian bombesin binds and functions approximately fourfold better than GRP itself at the mammalian bombesin/GRP receptor, apparently due to conformational differences related to its lower molecular weight that permit greater access to GRPR cell-surface receptors in tissues (2325). Cumulatively, these observations provided our rationale for choosing bombesin as well as GRP for the present studies. To evaluate the possible contribution of other bombesin-related peptides, we also tested NMB and a synthetic BRS3 ligand (26). Subsequent studies in GRPR, NMBR, and BRS3 knock-out (KO) mice were performed to determine which receptor might be mediating alveolar changes in response to BLP.

Finally, the experimental design was chosen in an attempt to recapitulate the molecular events occurring in infants that develop BPD (27). In human infants with BPD, an elevated BLP level in the first 5 d after birth is a strong risk factor for developing BPD 2–3 mo later. In 2 baboon models of BPD, elevated BLP in the first 3 d after birth was closely correlated with impaired pulmonary function 10–21 d later.

This work was presented in part at the meeting of the Pediatric Research Society in 2002 (28).


The National Institutes of Health Guide for the Care and Use of Laboratory Animals was strictly adhered to throughout this study.

Timed-pregnant Swiss Webster mice were from Charles River Laboratories (Wilmington, MA). GRPR-, NMBR-, and BRS3-KO mice were inbred into a C57BL/6 background for 10 generations or more. Tail DNA was prepared as previously described (20, 22). Mice were genotyped using polymerase chain reaction for GRPR, NMBR, and BRS3 as previously described (20, 22). Wild-type (WT) littermates were the matched control animals for the KO mice in all experiments. Mice were killed on Postnatal Day 14 using CO2, lungs were inflated in situ (details given in online supplement) and fixed overnight in 4% paraformaldehyde, then processed into paraffin.

Experimental mice were divided into four groups. Groups 1 and 2 are referred to as “prenatal,” and Groups 3 and 4 as “postnatal”:

  • Group 1: bombesin at 200 μg/kg in phosphate-buffered saline (PBS) was administered intraperitoneally twice daily to pregnant mice at Embryonic Days 14–16 (8).

  • Group 2: an equal volume of PBS was given intraperitoneally in parallel with Group 1.

  • Group 3: Bombesin was given intraperitoneally twice daily for 3 d to pups beginning at 24 h of age (P1–P3). In some experiments, GRP, NMB, or BRS3 ligand were tested using doses at equivalent molarity to 200 μg/kg bombesin. Bombesin, GRP, and NMB were from Peninsula Laboratories (San Carlos, CA). The BRS3 ligand was provided by Dr. David Coy at Tulane University, New Orleans, LA (26).

  • Group 4: an equal volume of PBS was given intraperitoneally twice daily at P1–P3. Mice were weighed daily to determine the proper volume for 200 μg/kg/injection. This dose was previously determined to elicit significant responses in fetal mouse lung (8).


A variation of the avidin-biotin complex technique was used (16). Detailed methods are given in the online supplement. The primary antibodies are mouse monoclonals: anti–α-smooth muscle actin (SMA): clone 1A4 (Sigma, St. Louis, MO); and anti–proliferating cell nuclear antigen (PCNA): clone PC10 (Dako, Carpinteria, CA).

Morphometric Analyses

Digitized images were captured at 20× magnification using a Nikon Labphot camera (Nikon, Tokyo, Japan). A total of 8–20 20× images were taken randomly from each lung lobe per mouse, using nonoverlapping fields at 3, 6, 9, and 12 o'clock.


The percentage of nuclei with PCNA staining was calculated as follows: (no. PCNA-positive cells)/(total no. nucleated cells, both positive and negative) × 100%.


A 365-point grid was superimposed on each captured field. The volume–percent of SMA-positive lung tissue was calculated as follows: (total number of SMA-positive points)/(365 − [positive points over airspaces]) × 100%.

Alveolar wall thickness.

Using the same images, approximately 60–80 lines per field were drawn perpendicular to the narrowest segment of primary and secondary alveolar septa. The mean length of lines crossing the septa was determined using Scion Image (Scion Corp., Frederick, MD) (29).

Mean linear intercept.

Using a predetermined grid with randomly distributed lines totaling 1-mm in length, mean linear intercept (MLI) was calculated as follows: 1/(no. air–tissue interfaces) × 1000, yielding the average distance between two air–tissue interfaces in microns.

Statistical Analysis

Data are given as mean ± SEM, determined using one-way analysis of variance. Statistical significance was defined as p < 0.05.

PCNA Immunostaining

The first approach of the current investigation was to determine whether bombesin treatment alters cell proliferation in developing postnatal lung, because BLP was previously demonstrated to be to be a potent growth factor for normal bronchial epithelial cells, lung cancer cell lines, and fetal lung (2, 8, 30). We performed immunostaining for the cell cycle–specific marker, PCNA, which is expressed only by actively dividing cells with a half-life of 20 h. We chose the experimental design described here in an attempt to recapitulate the molecular events occurring in infants that develop BPD, who have elevated BLP levels shortly after birth followed by lung disease weeks to months later (16, 27).

Representative photomicrographs are given in Figure 1. Compared with PBS-treated control mice (n = 6) (Figure 1A), pups treated with bombesin either prenatally or postnatally (n = 8–9 in each group) (Figure 1B) had increased relative numbers of PCNA-positive lung cells. The increased PCNA labeling was localized predominantly to alveoli (Figure 1B, red arrows), but was also evident in airway epithelium (Figure 1B, black arrows), as compared with PBS-treated control animals (Figure 1A). Morphometric analyses demonstrated a threefold increase in the percentage of nuclei that were PCNA-positive, both in the developing alveoli (Figure 1C) and in airway epithelium (data not shown). Mice treated either prenatally or postnatally had essentially identical bombesin-induced PCNA responses.

To identify which cells are proliferating in the developing alveoli, we performed immunofluorescence analysis for SMA (green) and surfactant protein C (SPC; red) in slides that had been previously immunostained for PCNA. Representative results from a mouse treated postnatally with bombesin are given in Figure 1D. Over 80% of the PCNA-positive cells (left panel) were also SMA-positive (Figure 1D, arrows indicate cells with cytoplasmic SMA green fluorescence superimposed on PCNA-immunopositive nuclei). Less than 5% of the PCNA-positive cells were SPC-positive (Figure 1E, long arrow). About 10–20% of the PCNA-positive cells did not label with either SMA or SPC, and most of these appeared to be airway epithelial cells, endothelial cells, or inflammatory cells (data not shown).

PCNA labeling was then examined in untreated KO mice on a C57BL/6 background. The untreated KO mice were age-matched with the bombesin-treated KO mice (i.e., 14 d of age), when alveolarization was about half complete. For all three BLP receptors (GRPR, NMBR, and BRS3), the same observation was made: at baseline, there was no significant difference in PCNA labeling between KOs (n = 7) and WT littermates (n = 7) (Figure 2A). Also, there was no difference in PCNA labeling between untreated mice and mice treated with PBS postnatally, in either KO or WT mice (data not shown).

Next, we evaluated PCNA labeling in KO mice treated postnatally with bombesin. We used only postnatal treatment because the KO mice have reduced fertility, which limited the number of feasible experiments. The results of three experiments are given in Figure 2, with pooled results of quantitative morphometry summarized in Figure 2A. Compared with untreated WT C57BL/6 mice (Figure 2A), bombesin-treated WT C57BL/6 pups had a doubling in the percentage of alveolar cells with PCNA-positive nuclei (Figures 2A and 2B, red arrows). In the same animals, there was no difference in PCNA labeling of airway epithelial cells. Paradoxically, bombesin-treated GRPR KO mice demonstrated significantly more PCNA labeling of cells in the distal lung (Figures 2A and 2C, red arrows). In contrast, there was no difference in relative numbers of PCNA-labeled nuclei between NMBR or BRS3 KO mice and their WT littermates (data not shown).

α-SMA Immunostaining

We next tested the hypothesis that bombesin treatment regulates interstitial fibrosis by altering the relative numbers of myofibroblasts, which are the proliferating subtype of fibroblasts involved in fibrotic reactions, and are SMA-positive.

In the first series of experiments, bombesin was given to Swiss-Webster mice either prenatally or postnatally, as described previously here, and lungs were harvested at P14. Representative photomicrographs of SMA-immunostained slides from mice treated postnatally are presented in Figures 3A and 3B (PBS- and bombesin-treated, respectively). By morphometric analysis (Figure 3C), there was a three-to fourfold increase in the volume percent of SMA immunostaining in mice given bombesin prenatally or postnatally compared with PBS-treated control mice. Much of this increase was in the form of interstitial SMA positivity (Figures 3A and 3B, red arrows), rather than the normal SMA positivity that occurs at the tips of developing septa (Figures 3A and 3B, black arrows). It should be noted that SMA positivity associated with airways (data not shown) and blood vessels (Figures 3A and 3B, V, red asterisk) was excluded from the analysis. The magnitude of these data are similar to results with PCNA immunostaining (described previously here).

In the second series of experiments, SMA labeling was analyzed in untreated KO mice (on a C57BL/6 background) and their WT littermates. GRPR-null mice (n = 6) had a 1.5-fold increase in the volume percent of SMA staining when compared with control littermates (n = 7) (p < 0.02). However, in untreated NMBR and BRS3 mice, there was no significant difference in SMA labeling between KOs (n = 7) and WT littermates (n = 7) (data not shown). Also, there was no difference in SMA labeling between PBS-treated and untreated mice, in either KO or WT animals (data not shown).

In the third series of experiments, GRPR-null, NMBR-null, and BRS3-null pups were treated with bombesin intraperitoneally from P1–P3. Again, we chose to treat postnatally because the number of KO mice was limited and postnatal bombesin is most similar to the elevated BLP levels occurring postnatally in premature infants with elevated BLP during the period of alveolarization. The results of these experiments are given in Figure 4. Bombesin-treated GRPR WT pups had a twofold increase in interstitial SMA positivity (p < 0.001 compared with untreated WT control animals), which was predominantly interstitial (Figure 4B, red arrows) rather than at developing septal tips (Figure 4B, black arrows). In contrast, bombesin-treated GRPR KO pups had increased SMA-positivity representing about a threefold increase over baseline values for the untreated KO mice (p < 0.001). Most of this SMA immunoreactivity was interstitial (Figure 4C). Bombesin-treated KO mice had significantly more SMA positivity compared with bombesin-treated WT littermates (p < 0.001).

There was no significant difference in SMA staining for either NMBR-null or BRS3-null mice (n = 3 each) compared with their WT littermates (n = 5) (data not shown). These data are consistent with the increased PCNA immunostaining in lung parenchyma of GRPR-null mice compared with their WT littermates.

Alveolar Wall Thickness

During the initial slide review, we observed increased interstitial thickness as a prominent and consistently noticeable feature of the bombesin-treated lungs. Alveolar wall thickness was measured in a rigorous and exhaustive fashion, restricting the analysis to lobes that were well inflated. Using the hematoxylin and eosin–stained slides, we measured alveolar wall thickness in PBS-treated Swiss Webster mice (n = 6–8; Figure 5A) and pups from the same litters treated with bombesin (n = 8–10; Figure 5B). The pooled results of these quantitative analyses are given in Figure 5C. There is a significant increase (∼ 24–27%) in alveolar wall thickness in bombesin-treated mice as compared with control mice (p < 0.0001), whether mice were treated prenatally or postnatally. These data are highly significant and closely correlate with increased numbers of proliferating SMA-positive cells in the interstitium. The same results of increased alveolar wall thickness were obtained with GRP treatment of C57BL/6 mice. In contrast, GRP-treated GRPR KO mice did not demonstrate any increase in alveolar wall thickness compared with untreated GRPR KO littermates, whereas GRPR WT littermates did have increased alveolar wall thickness with GRP treatment (data not shown).


As a general index of lung growth and alveolar development, we measured lung weights and volumes, which were then normalized for the total body weight of each pup. There were no significant differences between the groups (data not shown), but there was considerable variability within each group. Some of this variability could be related to the difficulty in measuring accurate lung volumes on the small P14 lungs.

We turned to a more specific measurement of alveolar septal development: MLI, measured as described in Methods. In outbred Swiss-Webster mice, there was no significant difference in MLI between bombesin-treated and PBS-treated pups (data not shown). However, there was a significant bombesin-induced decrease in alveolarization in GRPR-WT mice, which are inbred onto a C57BL/6 background for over 12 generations. As shown in Figure 6A, untreated GRPR-WT mice have well developed alveoli at Postnatal Day 14; PBS-treated GRPR-WT mice appeared identical (data not shown). At baseline, GRPR-KO mice had the same MLI (Figure 6B) as the WT littermates (Figure 6A). Bombesin-treated GRPR-WT mice had a marked increase in the MLI (1.5-fold), reflecting fewer alveolar septa and larger alveoli (Figure 6C). Bombesin-treated GRPR-KO mice also had increased MLI (Figure 6D), but this increase was smaller in magnitude (1.25-fold) than that in the WT littermates. The average MLI for each group is given in Figure 6E. There was a significant difference in MLI between bombesin-treated GRPR-KO and bombesin-treated WT mice (p < 0.001).

We performed additional experiments treating newborn mice with GRP, NMB, and a synthetic BRS3 ligand, (DTyr6,[R-Apa11, Phe13, Nle14]Bombesin-[6–14]) (31), using doses that are equimolar to 200 μg/kg bombesin (detailed in the online supplement). GRP has the same effects on alveolarization as bombesin (Figure 6F). The effect of GRP on alveolarization was completely abrogated in GRPR KO mice (Figure 6F), indicating that this effect is entirely mediated by the bombesin/GRP–preferring receptor. In contrast, NMB had no effect on lung histopathology (data not shown). We also tested the synthetic BRS3 ligand (31) according to the same protocol, but no effects on lung histopathology were observed (data not shown). In summary, it appears that GRP is the mammalian peptide relevant to decreased alveolarization because GRP elicits the same responses as bombesin, whereas equivalent doses of NMB or a BRS3 ligand have no effect. GRPR mediates all of the GRP effects and much of the bombesin effect on alveolarization, but we do not know which receptor is mediating the remainder of the decreased alveolarization or the interstitial fibrosis in response to bombesin.

The objective of the present study was to test two hypotheses: (1) elevated BLP levels during perinatal development can lead to changes in lung histopathology that are characteristic of BPD; and (2) effects of BLP on developing lung are mediated via one or more of the three cloned mammalian BLP receptors. The major histopathologic changes that we observed were: (1) a significant increase in alveolar wall thickness that closely correlates with increased numbers of proliferating SMA-positive cells in the interstitium; and (2) a significant decrease in alveolarization in C57BL/6 (but not Swiss-Webster) mice.

Our observations support the hypothesis that GRP contributes to the interstitial fibrosis and decreased alveolarization that are characteristic of BPD (12). It is intriguing that an early elevation in bombesin or GRP levels in newborn mice could result in altered alveolar structure weeks later. We chose the described experimental design in an attempt to recapitulate the sequence of events occurring in infants that develop BPD. In human infants with BPD, an elevated BLP level in the first 5 d after birth confers a 10-fold increased risk for developing BPD 2–3 mo later (15). In two baboon models of BPD, elevated BLP in the first 3 d after birth is closely correlated with impaired pulmonary function 10–21 d later (16). There is no correlation between early BLP elevation and early parameters of lung function, nor is there any correlation between late BLP elevation (at 10–14 d) and late impairment of pulmonary function (16) (M. Sunday, unpublished data). These observations are reminiscent of rat studies in which prenatal dexamethasone resulted in altered alveolar structure at Postnatal Day 14, but not Postnatal Day 2 (32). Although we do not yet know the mechanism for the observed late effects of early bombesin treatment, it should be kept in mind that bombesin can function as a neuroregulatory hormone, altering the production of other regulatory peptides, including insulin and adrenocorticotropic hormone, and modulating expression of growth factor receptors, such as EGFR and GRPR (33). In previous work, we demonstrated that the same dose of bombesin is locally active over a short time course in mice in utero or in fetal lung organ cultures (8). The present study extends those earlier experiments by addressing late consequences of early BLP elevation. The late PCNA labeling is consistently elevated in pups treated early with bombesin, consistent with a late effect that is likely downstream from the initial BLP binding to its cognate receptor, via a mechanism that is secondary or indirect.

In newborn mice, GRP has the same effects on alveolarization as bombesin, and these effects are completely abrogated in GRPR KO mice, indicating that GRPR mediates this effect of GRP. In contrast, neither NMB nor a BRS3 ligand has any effect on lung histopathology. Our observations are consistent with numerous pharmacokinetic studies indicating that GRP and bombesin are nearly identical in mammalian systems, due to their shared bioactive amidated carboxyterminal sequence, both binding to the same high-affinity bombesin/GRP–preferring receptor. In fact, amphibian bombesin binds to and functions better at the mammalian bombesin/GRP receptor than does GRP itself, probably due to conformational differences related to its smaller molecular weight that permit greater access to the cell-surface GRPR in tissues (2325). Three of the four amino acids required for high-affinity bombesin binding to GRPR are also required for high-affinity GRP binding (34, 35). The peptide-specific binding site for GRP has been mapped to the third extracellular domain (35), whereas NMB selectivity has been mapped to the fifth transmembrane region (36). Four times as much GRP or 300 times as much NMB is required to elicit the same responses as bombesin (on a molar basis) at the bombesin/GRP–preferring receptor (23). It is also known that bombesin does not appreciably bind to the BRS3 receptor (26, 34). In some experimentally mutated receptors, however, bombesin has markedly higher affinity than does GRP (35), suggesting that a novel bombesin receptor could, in fact, mediate effects of bombesin that might persist in GRPR KO mice, as observed with bombesin-induced interstitial fibrosis and decreased alveolarization in the present study.

Normally, both GRP and the GRPR are expressed at low or undetectable levels after birth, when alveolarization normally takes place (33). Previously, we demonstrated that BLP promotes growth and maturation of fetal murine lung (8, 37). In the present study of bombesin-treated outbred mice, we demonstrate a threefold increase in both cell proliferation and the prevalence of myofibroblasts in the distal lung parenchyma, consistent with early signs of pulmonary interstitial fibrosis, such as occurs with BPD. Bombesin-treated GRPR KO mice had increased interstitial fibrosis (distal parenchymal cell proliferation and increased myofibroblasts) that was significantly greater than that in bombesin-treated GRPR-WT littermates. These data suggest that GRPR does not mediate this effect of bombesin, and could even protect against pulmonary interstitial fibrosis in newborn mice, or simply that a novel BLP receptor mediating the fibrosis is upregulated in a compensatory fashion in the absence of GRPR. Interestingly, GRP-induced interstitial thickening was completely abrogated in GRPR KO mice, further supporting the concept that a novel receptor may be mediating the bombesin effect on interstitial fibrosis.

It is unlikely that upregulation of NMBR and/or BRS3 would account for the above observations in bombesin-treated GRPR KO mice. First, neither NMB nor a synthetic BRS3 ligand had any effect on lung histopathology in the described protocol. Also, we did not observe any differences in mRNA levels for NMBR or BRS3 in newborn GRPR KO mice. Finally, NMBR and BRS3 KO mice had the same responses to bombesin as their normal littermates, further arguing against the involvement of NMBR and BRS3 in these responses.

Cumulatively, these observations suggest that a novel BLP receptor may mediate the effects of bombesin on alveolarization (in part) and interstitial thickening in developing lung. One possibility might be a mammalian phyllolitorin receptor. Bronchoalveolar lavage fluid from smokers has been found to have high levels of bombesin-like immunoreactivity most consistent with a mammalian phyllolitorin (38). Phyllolitorins can stimulate cell proliferation and branching morphogenesis in murine embryonic lung buds (11). An amphibian phyllolitorin has been cloned (39), but its mammalian homolog and a phyllolitorin receptor have yet to be identified. However, phyllolitorins have only very low affinity for GRPR (23), so it seems unlikely that a mammalian phyllolitorin receptor reciprocally would mediate the bombesin-induced effects observed in the present study.

Our analyses of alveolar development after bombesin treatment have yielded additional novel observations. First, bombesin diminished alveolarization in C57BL/6 mice, but not in outbred Swiss-Webster mice, suggesting that this response depends on background genes that are as yet unidentified. Second, GRPR-KO mice are protected in part against this inhibitory effect of bombesin on alveolarization, indicating that GRPR mediates a significant part of the reduced alveolarization. These observations are of particular interest because only a subset (∼ 30%) of premature infants develop BPD (40), and twin studies indicate that genetic factors play an important role in human BPD (41). Similarly, it has been suggested that elevated BLP levels in humans might predict which adult patients will develop smoking-related lung diseases, including emphysema (42). Analogous to BPD developing in less than a third of oxygen-treated preterm infants, only about 20% of smokers develop chronic lung disease, and these appear to be the same patients that have elevated BLP levels (43). Thus, increased BLP receptor signaling due to increased BLP levels could be a common denominator for lung diseases with decreased alveolarization, including both BPD and emphysema.

The observed dissociation between interstitial fibrosis and diminished alveolarization supports the concept that BPD can result from the activation of multiple signaling pathways, even when a single peptide (bombesin or GRP) is used to mimic the effect of hyperoxia in a premature infant. We have demonstrated that increased BLP levels in baboons with BPD are directly linked to oxidant exposure, because treatment of animals with a novel antioxidant abrogates these increased BLP levels (18, 44). Similarly, GRP may have a role in acute lung injury (16, 45). In view of the fact that BPD is a multifactorial disorder, it remains surprising that several characteristic histopathologic features of BPD can be induced by a single peptide in a simple newborn mouse model. The present study suggests that early overproduction of BLP by pulmonary neuroendocrine cells might be sufficient to trigger the cascade of events leading to arrested alveolarization and interstitial fibrosis. In conclusion, it appears that GRP is the relevant mammalian peptide because it elicits the same responses as bombesin, whereas neither NMB nor a BRS3 ligand has any effect. Detailed mechanisms underlying these complex developmental pathobiological effects remain to be explored.

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31. Mantey SA, Coy DH, Pradhan TK, Igarashi H, Rizo IM, Shen L, Hou W, Hocart SJ, Jensen RT. Rational design of a peptide agonist that interacts selectively with the orphan receptor, bombesin receptor subtype 3. J Biol Chem 2001;276:9219–9229. Epub 2000 Dec 8.
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34. Nakagawa T, Hocart SJ, Schumann M, Tapia JA, Mantey SA, Coy DH, Tokita K, Katsuno T, Jensen RT. Identification of key amino acids in the gastrin-releasing peptide receptor (GRPR) responsible for high affinity binding of gastrin-releasing peptide (GRP). Biochem Pharmacol 2005;69:579–593. Epub 2004 Dec 23.
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38. Aguayo SM, Kane MA, King TE, Schwarz MI, Grauer L, Miller YE. Increased levels of bombesin-like peptides in the lower respiratory tract of asymptomatic cigarette smokers. J Clin Invest 1989;84:1105–1113.
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41. Parker RA, Lindstrom DP, Cotton RB. Evidence from twin study implies possible genetic susceptibility to bronchopulmonary dysplasia. Semin Perinatol 1996;20:206–209.
42. Aguayo S, King T, Kane M, Sherritt K, Silvers W, Nett L, Petty T, Miller Y. Urinary levels of bombesin-like peptides in asymptomatic cigarette smokers: a potential risk marker for smoking-related diseases. Cancer Res 1992;52(Suppl. 9):2727s–2731s.
43. Aguayo SM. Determinants of susceptibility to cigarette smoke. Am J Respir Crit Care Med 1994;149:1692–1698.
44. Chang L, Subramaniam M, Yoder BA, Day BJ, Coalson JJ, Sunday M, Crapo JD. A catalytic antioxidant attenuates alveolar structural remodeling in bronchopulmonary dysplasia. Am J Respir Cell Mol Biol 2003;167:57–64.
45. Dal-Pizzol F, Di Leone LP, Ritter C, Martins MR, Reinke A, Pens Gelain D, Zanotto-Filho A, de Souza LF, Andrades M, Barbeiro DF, et al. Gastrin-releasing peptide receptor antagonist effects on an animal model of sepsis. Am J Respir Crit Care Med 2006;173:84–90. Epub 2005 Sep 28.
Correspondence and requests for reprints should be addressed to Mary E. Sunday, M.D., Ph.D., Department of Pathology, Duke University Medical Center, Box 3712, Durham, NC 27710. E-mail:


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