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Laminins and their integrin receptors are implicated in epithelial cell differentiation and progenitor cell maintenance. We report here that a previously unrecognized subpopulation of mouse alveolar epithelial cells (AECs) expressing the laminin receptor α6β4, but little or no pro–surfactant C (pro-SPC), is endowed with regenerative potential. Ex vivo, this subpopulation expanded clonally as progenitors but also differentiated toward mature cell types. Integrin β4 itself was not required for AEC proliferation or differentiation. An in vivo embryonic lung organoid assay, which we believe to be novel, was used to show that purified β4+ adult AECs admixed with E14.5 lung single-cell suspensions and implanted under kidney capsules self-organized into distinct Clara cell 10-kDa secretory protein (CC10+) airway-like and SPC+ saccular structures within 6 days. Using a bleomycin model of lung injury and an SPC-driven inducible cre to fate-map AECs, we found the majority of type II AECs in fibrotic areas were not derived from preexisting type II AECs, demonstrating that SPC– progenitor cells replenished type II AECs during repair. Our findings support the idea that there is a stable AEC progenitor population in the adult lung, provide in vivo evidence of AEC progenitor cell differentiation after parenchymal injury, and identify a strong candidate progenitor cell for maintenance of type II AECs during lung repair.
Basement membrane laminins and their integrin receptors are critical to lung development and implicated in epithelial cell differentiation and progenitor cell maintenance (1–3). There are 3 major integrin laminin receptors, all of which are expressed in the lung and primarily in epithelial cells: α3β1, α6β1, and α6β4 (4). α6β4 is thought to be particularly important in epithelial cell adhesion to basement membranes because this integrin has a uniquely long cytoplasmic tail that promotes assembly of α6β4 into hemidesmosomes (5). In humans, mutations of either α6 or β4, which only partners with α6, are known to result in varying degrees of a blistering skin phenotype depending on the degree of loss of integrin function (6). Skin blistering and sloughing of mucosal epithelial cells have also been reported in integrin β4–deficient mice (7). To define the role of this integrin in lung homeostasis, we generated mice with epithelial-specific deletion of integrin β4 and characterized the resulting effect on lung function. Unexpectedly, these mice appeared normal and had a normal lifespan. Although α6β4 is thought to be primarily localized to conducting airways of the lung, in the course of this work we discovered that a substantial fraction of distal lung/alveolar epithelial cells (AECs) expressing little or none of the canonical Clara cell 10-kDa secretory protein (CC10) or pro–surfactant protein C (pro-SPC) also expressed α6β4. These cells were found to clonally expand ex vivo and to be capable of multiple passages in culture, suggestive of a possible progenitor population and leading us to characterize their lineage potential both ex vivo and in vivo. While this work was in progress, a separate report indicated that epithelial cells isolated from single-cell preparations of whole lungs on the basis of α6β4 expression have stem-like properties ex vivo, but the location of these cells and their in vivo potential were not defined (8). We here confirmed the existence of a dynamic population of distal epithelial cells and demonstrated, using a lung organoid assay developed in our laboratory that we believe to be novel, the regenerative potential of these cells in vivo.
The replenishment of damaged epithelial cells in the lung parenchyma after injury is thought to depend on proliferation and differentiation of SPC+ type II cells. Indeed, the timing and extent of type II cell hyperplasia covering damaged alveolar basement membranes is thought to be a protective process that minimizes the fibrogenic program in the lung (9, 10). To address the question of whether type II cells are in fact the major cell type repopulating damaged lung, we developed an in vivo fate-mapping system using tamoxifen-inducible cre recombinase placed within the endogenous SPC locus. These experiments instead revealed a clear role for progenitor cells in lung repair, consistent with our finding that immature epithelial progenitors existed and responded dynamically to injury. Collectively, these findings provide insights into the pathophysiology of lung repair.
Mice with selective lung epithelial loss of α6β4 (referred to herein as Fβ4SC mice) were generated by crossing floxed integrin β4 mice with mice carrying the human SPC promoter-rtTA and tetO-CMV-Cre transgenes (refs. 11, 12, and Supplemental Figure 1A; supplemental material available online with this article; doi: 10.1172/JCI57673DS1). Lung epithelial-specific recombination of triple transgenics was verified by immunostaining for β4 (Supplemental Figure 1C). In sections, β4 was detected in near-linear basilar staining of airway cells throughout the conducting airways that colocalized with basement membrane laminin 5 (Supplemental Figure 1, C and D). In Fβ4SC mice, there was marked loss (range, 75%–90%, n > 12) of integrin staining in all distal conducting airways lined by a layer of cuboidal epithelial cells, but much less or no loss in more proximal airways lined by ciliated cells (Supplemental Figure 1, B–D), consistent with prior reports of cre expression patterns in this transgenic system (13). Inspection of Fβ4SC mice indicated that adult mice had no discernible morphological abnormalities in their lungs.
To assess the role of α6β4 during injury and repair, Fβ4SC mice were injected with saline or bleomycin (2.5 U/kg) intratracheally (12). Lung permeability at baseline and after 5 days was not different between WT and Fβ4SC mice (Supplemental Figure 2A). However, beginning at approximately day 6, Fβ4SC mice began to die, and most succumbed by day 14, whereas WT mice mostly survived (Supplemental Figure 2B). Inspection of the lungs of Fβ4SC mice at 6–10 days after bleomycin injection showed marked sloughing of intact epithelial sheets from the distal airways (Supplemental Figure 2C). These findings are consistent with prior observations of integrin β4 deficiency in skin and nasal mucosa (7) but indicate that, in the lung, epithelial cells appear to remain adhesive until stressed. Although we cannot be sure that the mice die of epithelial sheet sloughing in conjunction with the alveolar injury induced by bleomycin, this complication appears likely to exacerbate the degree of injury and precipitate death.
Fβ4SC mice were also examined after airway injury with naphthalene (14). Both WT and Fβ4SC mice survived the injury and by day 14–21 showed near-complete recovery of CC10+ lining cells. Immunostaining confirmed that repopulating Clara cells in the bronchioles of Fβ4SC mice had undetectable integrin β4. Thus, although α6β4 was required for strong adhesion, the integrin per se was not required for proliferation and/or differentiation of these cells during repair, consistent with prior studies of α6β4 deficiency in keratinocytes (11).
Flow cytometric analysis of preparations of type II alveolar cells revealed expression of α6β4 on a small fraction (8%–10%) of AECs (Figure (Figure1A).1A). The presence of α6β4 in a minor population of AECs raised the possibility that α6β4 expression might reveal population heterogeneity among AECs, as suggested by prior studies (14–16). β4+ cells were located both in the bronchoalveolar junction regions and within alveoli (Figure (Figure1C1C and Supplemental Figure 3). Notably, the pattern of β4 staining changed near the junction region and within alveoli. Whereas in the bronchiolar and larger airways, β4 staining was quite basilar in hemidesmosomes, in the junctional regions, β4 was more diffuse and difficult to detect. Costaining with the Clara cell marker CC10 indicated that only some junctional cells were β4+, and these appeared to have lower CC10 expression (Figure (Figure1C).1C). CC10–β4+ cells were also found sporadically (less than 1 per ×20 field) in alveolar walls (Figure (Figure1C1C and Supplemental Figure 3), where they did not colocalize with pro-SPC. Both junctional and alveolar β4 staining was largely lost in Fβ4SC mice (Supplemental Figure 1C).
To assess the relative airway and alveolar contributions to the β4+ AEC population, cytospins of freshly isolated cells were analyzed with antibodies to mature epithelial cell types. Cytospins of β4– AECs purified by flow cytometry were almost uniformly SPChi and CC10–, indicating mature type II AECs, whereas more than 80% (83% ± 10%, n = 4) of β4+ AECs were dim or negative for SPC and CC10 (Figure (Figure1B).1B). These cells were also not stained with the type I AEC marker T1α, and ciliated cells were not observed. A portion of β4+ cells were strongly CC10+ (9% ± 3%), likely reflecting contamination with Clara cells, which suggests that the β4+ cell population is itself heterogeneous. Less than 1% of the purified β4+ cells were SPC+. Given that the fraction of CC10+ cells within the β4+ cell population is less than 10%, and yet β4+ cells represent 8%–10% of all AECs, we interpret this result to mean that the majority of β4+ AECs low or negative for SPC and CC10 in our preparations must come from the alveolar compartment. To date, we have no method to reliably separate β4+ cells located in terminal airways/bronchoalveolar junctions from those within alveoli; thus, the term β4+ AEC used herein encompasses mainly alveolar cells, but also terminal airway/junctional cells.
β4+ cells were purified from standard AEC preparations by positive E-cadherin antibody selection followed by sorting for β4+ cells. Immunoblotting confirmed that the β4+ and β4– cell populations were distinct (Figure (Figure2A).2A). β4+ AECs cultured on Mg developed large cell colonies within 7 days, whereas β4– AECs remained as single cells or small clusters (Figure (Figure2B).2B). Ki67 staining confirmed proliferation within the developing colonies of β4+ AECs (Figure (Figure2B),2B), and quantitative BrdU incorporation revealed that greater than 90% of the proliferative potential of AECs resided in the β4+ fraction (Figure (Figure2C).2C). The colonies of β4+ cells could be recovered (by pipetting) and passaged onto new Mg for at least 6 passages. Differential cell counts of dispersed, single colonies (n = 12) that had expanded over 7 days revealed colony heterogeneity. The colonies were greater than 60% SPC–CC10–, but almost all colonies now also contained both SPC+ (22% ± 30%) and CC10+ (13% ± 6%) cells. Accounting for the large SD for this marker, 2 colonies were exclusively SPC–CC10–, and 2 colonies were exclusively SPC+. A small percentage (3% ± 3%) was SPC+CC10+, a cell type never observed among the freshly isolated β4+ AECs. Notably, approximately 10%–15% of the colony cells were β4–, indicative of some tendency to lose this marker in culture. Colony formation by β4+ AECs plated on irradiated embryonic feeder fibroblasts for 1–2 weeks was not observed.
To determine the role of integrin β4 in the proliferation of β4+ AECs, β4+ AECs were isolated from mice homozygous for the nonrecombined conditional β4 allele and treated with cre recombinase for 72 hours ex vivo. Remarkably, colonies that emerged in 7 days were exclusively β4– or β4+, and the sizes of the colonies were indistinguishable (Figure (Figure2D),2D), which indicates that these colonies likely developed independently of β4 and from single cells. To further explore the latter point, β4+ AECs were purified from transgenic mice constitutively expressing either GFP or tomato red fluorescent protein. When single β4+ cell suspensions from either mouse were mixed and placed in culture, all of the individual colonies (n = 65) were exclusively red or green, indicative of clonal expansion rather than cell aggregation (Supplemental Figure 4). This observation, together with the finding of both CC10+ and SPC+ cells in 1 β4+ colony, implies that single SPC– or CC10– β4+ AECs can differentiate in culture into cells with markers of either airway or alveolar cells. We next attempted to test the progenitor potential of β4+ AECs in vivo.
Prior studies have demonstrated that dissociated mouse E14.5 lung cells cultured as high-density mixed cell aggregates (lung organoids) at an air-fluid interface can form lung histotypic structures, including alveolar-like spheres, lined by appropriately differentiated epithelial cells (17). We have improved upon this method to achieve extensive development of lung organoids in vivo that recapitulated normal development. We implanted high-density mixed cell aggregates (organoids) prepared from single-cell suspensions from E14.5 lungs underneath the renal capsule of immunodeficient (nude) mice. These grafted lung organoids grew and became easily visible after 6 days (Figure (Figure3,3, A and B). This model was highly reproducible, and almost all engraftments resulted in fully developed organoids. Notably, a vasculature developed within the structure and connected with the host vasculature, as rbcs were apparent in tubular structures within the grafts (Figure (Figure3C).3C). Graft development required both epithelial and mesenchymal cells, which indicates that specific cell populations can be examined for their developmental potential in this assay.
Examination of histological sections of the grafts at days 2–6 showed that the grafts underwent a series of developmental stages resembling that of normal embryonic lung (Figure (Figure3D):3D): day 2 grafts resembled pseudoglandular-stage lungs, containing epithelial tubes surrounded by abundant mesenchyme; day 4 grafts resembled canalicular-stage lungs, containing epithelial tubes lined by columnar epithelial cells typical of proximal airways as well as branching structures lined by more flattened epithelial cells typical of distal airspaces; and day 6 grafts contained structures resembling saccules composed of interconnected airspaces lined by flattened epithelial cells, typical of E18.5 lungs. To directly test whether the embryonic single-cell suspensions are both organizing and differentiating under the kidney capsule, organoid sections were immunostained for CC10, SPC, and Pecam-1. E14.5 lungs showed SPC in airway epithelial cells (Supplemental Figure 5B), whereas in the day 5 organoid, SPC was found in cells lining saccular structures (Figure (Figure3,3, E and F, and Figure Figure4,4, A and C), consistent with the pattern of SPC expression in saccular-stage lungs. CC10 was not detectable in day 14.5 lungs (Supplemental Figure 5B), since it is normally found only at low levels starting at E15.5 and increases thereafter (18, 19). In day 5 organoids, vivid CC10 staining was apparent in cuboidal epithelial cells (Figure (Figure3F3F and Figure Figure4B),4B), consistent with expression in bronchiolar epithelial cells. Strikingly, there were virtually no SPC+CC10+ cells and even little mixing of single-positive cells. Regions of the developing organoid were commonly CC10+ airway-like, leading into “blind” SPC+ saccules (Figure (Figure3F).3F). True quantification of the fraction of airway and saccular structures was not attempted, but SPC+ saccules were always more abundant than CC10+ airway-like structures. Whether all saccules were connected to an airway-like structure could not be reliably assessed. We next tested the potential of adult β4+ or β4– AECs to incorporate into and differentiate in the developmental environment of a lung organoid.
Organoids were made from E14.5 lung cells depleted of epithelial (E-cadherin+) cells and reconstituted with purified β4+ or β4– AECs admixed with E-cadherin+ embryonic cells in various ratios and grafted under the renal capsule for 5–6 days. Preliminary experiments indicated that a 1:10 ratio of adult AECs to embryonic epithelial cells resulted in organoids similar in size to unperturbed E14.5 cell suspensions. Under these conditions, GFP+β4– AECs only occasionally persisted as single cells in the organoids, but were unable to form discernible structures (Supplemental Figure 5A). However, GFP+β4+ AECs were found to organize and incorporate extensively into the developing lung organoids (Figure (Figure4A).4A). As evident in the scanning view (Figure (Figure4A),4A), GFP+ cells were not distributed as single cells, but instead appeared as foci or clusters of cells (Figure (Figure4,4, B and C). Closer inspection revealed that GFP+β4+ AECs developed into either discrete SPC+ saccules or CC10+ airway-like structures. There were only rare SPC+CC10+ cells and few SPC–CC10– cells: most GFP+β4+ AECs were at least weakly SPC+, if not CC10+. Intriguingly, the organoid structures developing from mixtures of embryonic/adult GFP+β4+ cells (10:1) were almost exclusively either wholly adult cell derived or wholly embryonic, indicative of a clear capacity for self-organization. This point is illustrated in Figure Figure4B,4B, which juxtaposes 2 airway-like structures lined by CC10+ cells, one fully of embryonic origin and the other fully derived from GFP+ cells. A similar pattern was observed with SPC+ saccules (Figure (Figure4C).4C). Collectively, these data indicate that adult β4+ AECs can both differentiate ex vivo and regenerate epithelial structures in vivo. The almost exclusive differentiation into distinct SPC+ or CC10+ structures, even though β4+ colonies ex vivo were multipotential (Figure (Figure2),2), indicates a strong influence of the organoid microenvironment on differentiation in vivo, a conclusion consistent with the spatial separation of CC10 and SPC expression in the day 6 embryonic organoid itself (Figure (Figure3D). 3D).
We next asked whether the pool size of β4+ AECs changes in response to injury. Mice were exposed to bleomycin (2.5 U/kg), and AECs were isolated after 14 days. Flow cytometry consistently showed an increased fraction of β4+ AECs 7–10 days after bleomycin injury (Figure (Figure5B).5B). In 5 experiments, the recovered β4+ cells increased on average from approximately 10% of the total AECs in saline-treated mice to 27% ± 10% in bleomycin-injured mice. This was reflected in increased amounts of integrin β4 assessed by immunoblotting of AECs recovered from bleomycin- compared with saline-injected mice (Figure (Figure5A).5A). Cytospins of the cells recovered from injured mice following sorting for β4 revealed substantially more CC10+ cells (20%), likely reflecting either increased airway contamination or bronchiolization of the alveoli, which was evident in sections of injured lung (Figure (Figure5,5, D and E). Still, the majority of recovered β4+ AECs after bleomycin injury remained low or negative for CC10 and SPC. Moreover, unlike the case with normal lungs, SPC+β4+ cells (4%) were recovered from bleomycin-injured lungs. Consistent with this observation, some alveolar β4+ cells in injured lungs also stained for SPC (Figure (Figure5C). 5C).
Given the increased numbers of β4+ AECs low or negative for CC10 and SPC — likely with progenitor potential — after parenchymal injury (Figure (Figure5),5), we asked whether maintenance of the type II cell population after major injury involves AEC progenitors. To address this issue, we created an inducible system for fate-mapping alveolar type II cells using homologous recombination. The terminal stop codon of the endogenous mouse SPC gene (exon 5; Figure Figure6A)6A) was replaced with an estrogen-dependent cre cDNA (CreERT2) preceded in frame by a E2A peptide sequence to interrupt translation between SPC and cre mRNAs coexpressed on a single transcript (20). A Nde1 site was introduced to facilitate ES cell screening, and correctly targeted clones were generated, as confirmed by Southern blotting (Figure (Figure6B).6B). ES cell–derived mice homozygous for the mutation showed normal SPC levels by immunoblotting, and cross-breeding of these mice with a cre-dependent transmembrane GFP (loxp-tm-TR/GFP) reporter strain revealed tamoxifen-inducible GFP expression specifically in type II cells (Figure (Figure6C).6C). In the absence of tamoxifen, less than 1 GFP+ cell per ×20 field was detected, whereas 50%–60% of all type II AECs were GFP+ 7 days after 2 total 4-hydroxy-tamoxifen i.p. injections (0.5 mg) 24 hours apart (Figure (Figure6C).6C). No GFP expression was observed in airway cells of tamoxifen-exposed mice, as expected.
A cohort of adult littermates expressing SPCcre-ER and loxp-tm-TR/GFP was injected with tamoxifen, and lungs were examined 7 or 30 days later. In some mice, bleomycin was injected intratracheally 14 days prior to sacrifice. The fraction of GFP+SPC+ cells was quantified by independent observers examining at least 10 ×20 fields of at least 3 sections of lung. The fraction of GFP+SPC+ cells 30 days after tamoxifen exposure (60% ± 10%) was not discernibly different from that observed at 7 days (Figure (Figure6D).6D). However, the fraction of GFP+SPC+ cells in fibrotic areas after bleomycin was markedly reduced to less than 15% (Figure (Figure6,6, D and E). This was not caused by global lack of cre expression, because some less-injured lung areas of the same mouse had vivid GFP expression in SPC+ cells (Figure (Figure6E).6E). Hyperplastic type II AECs lining alveoli within injured areas were consistently GFP– (Figure (Figure6E6E and Supplemental Figure 6). The reporter strain used in this analysis, loxp-tm-TR/GFP, also expressed tomato red fluorescent protein from the same allele in nonrecombined cells, and red fluorescence was easily detected throughout injured areas (Figure (Figure6F),6F), which indicated that the reporter gene itself was not silenced in bleomycin-injured lungs. Therefore, the data imply that SPC+ type II cells in day 14 bleomycin-damaged areas are largely derived from non–SPC-expressing progenitor cells existing at the time of injury. Similar results were observed in 4 independent experiments.
There is substantial evidence that the adult distal lung parenchyma, composed of bronchioles and alveoli, contains relatively quiescent epithelial cells that have proliferative and progenitor capacity (15, 21, 22). The current thinking is that Clara cells (or variant Clara cells with low CC10 expression) and alveolar type II cells are the main cell types with progenitor function in the distal lung parenchyma (22, 23). Our findings here showed that in the normal lung, α6β4 expression marked a strikingly fixed population of non–SPC-expressing AECs that possessed the capacity for proliferation and further differentiation ex vivo and regeneration of lung structures in vivo. These β4+ AECs were distinguished from Clara cells or alveolar type II cells by their lack of high levels of differentiation markers and the lack of proliferation of mature cells in culture (Figure (Figure2).2). β4+ AECs were found to reside in the bronchoalveolar junction regions, but also sporadically in alveolar walls. Based on the small fraction of CC10+ cells within the isolated β4+ AEC population and the observation that β4+ AECs accounted for almost 10% of total AECs recovered from normal lungs, the bulk of these cells appeared to be in the alveolar compartment, where they may be difficult to detect in situ because of diffuse distribution of α6β4. Diffuse staining of β4, indicative of dissolution of hemidesmosomes, has been previously observed in tumor cells (24). Although this population was stable in normal lungs, its proportion increased in bleomycin-injured murine lungs. In vivo, there was expansion of α6β4+ epithelial cells, some of which were either CC10+ or SPC+, into or within alveolar spaces during the fibrogenic phase of bleomycin injury. Finally, we provided the first direct evidence to our knowledge that maintenance of type II AECs after major lung injury prominently involved AEC progenitor differentiation and not simply expansion of preexisting type II cells. Although we cannot prove at this point that β4+ AECs within alveoli are the only progenitor source of type II AECs within the injured lung parenchyma, our data identify a strong candidate stem/progenitor cell that could account for these data. Further definition of the requirement for AEC progenitors in lung repair after different types and degrees of lung injury, and the specific requirement for β4+ AECs in this process, are important areas for further study.
While the present work was in progress, McQualter and colleagues reported the isolation of stem-like cells from adult mouse lungs using integrin α6β4 expression as a defining biomarker (8). Our findings support and extend this work. In the McQualter report, the starting material was a single-cell suspension of whole adult lung, but the location of the α6β4+ cells with stem-like properties in the lung could not be defined. No immunostaining for β4 in the bronchoalveolar regions or alveoli was observed. In contrast, the starting material for the present study were cells from the distal airways and alveoli. We were able to capitalize on the generation of a lung epithelial-specific β4-null mouse to verify that immunostaining for β4 in the bronchoalveolar and alveolar compartments was real. Nonetheless, in situ immunostaining appeared insensitive, and it is likely that at least a portion of the cells isolated by McQualter and colleagues is identical to the β4+ AECs described in this study.
This line of investigation emanated from the finding that only a fraction of primary AECs cultured ex vivo on fibronectin underwent epithelial-to-mesenchymal transition (EMT) when exposed to active TGF-β1, and this population proved to be mainly β4+ AECs (Supplemental Figure 7). There is accumulating evidence of functional similarities between the capacity of cells to undergo EMT and their display of stem-like properties (25). Our observations raise the possibility that EMT previously reported in vivo in mouse models of fibrosis (26) — and commonly thought to result from type II cells undergoing EMT — could mainly result from the enhanced plasticity of the β4+ AEC progenitors located in the normal lung and expanded after bleomycin injury in response to TGF-β1.
The in vivo organoid assay we developed and used herein is, to our knowledge, the first in vivo transplantation assay beginning with single-cell suspensions that recapitulates lung morphogenesis. Among the many possible applications of this assay, of particular interest here is our finding that adult β4+ AECs self-organized into structures bearing a single lineage marker in the day 6 organoids (Figure (Figure4).4). How these cells sort themselves from the more abundant embryonic epithelial cells and self-organize as they differentiate is currently unknown. The adult β4+ AECs used included cells located at the bronchoalveolar junction and within alveoli. One limitation of these experiments is that we cannot separate β4+ AECs present in the bronchoalveolar junction regions from those within alveoli, and thus we cannot determine to what degree cells from either site contribute to the CC10+ and SPC+ structures that developed in vivo (Figure (Figure4).4). Hence, we could not formally exclude the possibility that bronchoalveolar β4+ cells, rather than β4+ AECs, account for all progenitor activity in the organoid assay. However, we believe the findings that almost all colonies derived from single β4+ cells ex vivo contained SPC+ cells (Figure (Figure2)2) and that most β4+ cells appeared to reside within alveoli, where progenitor activity for type II cell maintenance appears important (Figure (Figure6),6), are more consistent with the view that β4+ AECs in both locations have progenitor potential, but their differentiation in vivo is restricted by their niches. This conclusion is consistent with prior in vivo evidence that bronchoalveolar CC10+ cells do not give rise to SPC+ cells in vivo, even after injury (22). It is likely that cells similar to the β4+ AECs exist in more than one anatomical niche, and it remains to be defined to what degree more proximal airway basal cells or other bronchiolar epithelial cells with stem cell properties (27, 28) function similarly to β4+ AECs in the organoid assay.
The finding that a stable but dynamically responsive population of immature progenitor cells exists in the parenchyma of adult lungs and likely contributes to alveolar repair has implications for the pathogenesis of common lung diseases in which tissue remodeling is a dominant feature. The current thinking has been that SPC+ type II cells are the main stem cells of the alveolar compartment (9, 23). Our observations suggest instead that, at least in the context of severe insult, preexisting SPC– epithelial progenitors expand and contribute substantially to repair. However, little is known about the degree to which such cells contribute to resistance to alveolar unit loss under stress, such as with cigarette smoking, or promote pathological mesenchymal expansion during fibrogenesis. Understanding the determinants of β4+ AEC population size and how these cells expand, self-organize, and differentiate along particular lineages should provide further insights into the processes of lung repair, the foundation for better therapeutics.
β4loxP mutant mice and SPC and Cre transgenic mice were described previously (11, 26). Pregnant females were maintained on doxycycline throughout gestation, and resulting litters were genotyped as previously described (11, 26). Both β-actin promoter–driven GFP-expressing (Tg[CAG-EGFP]B5Nagy) and β-actin–driven tomato red/transmembrane GFP (Gt[ROSA]26Sortm4[ACTB-tdTomato,-EGFP]Luo), termed loxp-tm-TR/GFP, transgenic mice were obtained from Jackson Laboratories. Mice were engineered to express tamoxifen-responsive cre-ERT2 and rtTA in frame with SPC but separated by “self-cleaving” E2A/T2A peptide sequences (Figure (Figure6A)6A) using standard recombineering methodologies and 129/C57BL6 hybrid ES cells (iGeniousTL Inc.). See Supplemental Methods for details. All animal procedures were approved by the Institutional Animal Care and Use Committee of UCSF. All mice were bred and maintained in a specific pathogen–free environment.
Isolation of primary AECs was performed as previously described (8); see Supplemental Methods for details. In most experiments, suspended AECs from standard AEC preparations were further purified by positive selection for E-cadherin using MACS magnetic bead technology. These cells were then sorted for β4 expression with a rat monoclonal β4 antibody directly conjugated with Alexa 647 using a MoFlo Cell Sorter (Dako) within the UCSF Flow Cytometry Core Facility.
Isolated cells and 5- to 7-μm cryosections were stained by immunofluorescence, X-gal, or H&E as previously described (26). Cells were analyzed by flow cytometry using an LSR II cytometer (BD Biosciences) and FlowJo.
Where indicated in the figure legends, mosaic images were generated from multiple ×20 images captured on a Zeiss Axio upright fluorescent microscope and tiled using 10% image overlap by Axiovision 4.7 software.
Tissue and cells were lysed in RIPA buffer (150 mM NaCl, 50 mM Tris, pH 8.0, 1% Triton X-100, 0.5% sodium deoxycholate, 0.1% SDS, supplemented with protease and phosphatase inhibitors) and analyzed by immunoblotting (26).
Mouse E14.5 lungs were dissected, diced, and digested in 0.2% collagenase/dispase at 37°C for 45 minutes. The digests were washed and resuspended in medium (BGJB with 5% FBS, 1 mg/ml ascorbic acid, 1× penicillin/streptomycin). Debris was removed from mechanically dissociated cells through a 70-μm nylon cell strainer. The single-cell suspension was then centrifuged, washed, resuspended in culture medium, and counted. For each organoid, 2 × 106 embryonic cells in single-cell suspension were concentrated by centrifugation, and the suspension (approximately 5–8 μl) was pipetted onto a 13-mm polycarbonate filter with 8-μm pore size floating on culture medium. The organoids were placed in a CO2 incubator overnight, and then implanted under the renal capsule, as described previously (29). To assess the potential of adult β4+ AECs to incorporate into the organoids, β4+ AECs were isolated as described above and expanded for 7 days by culture on Mg, after which single-cell suspensions were mixed in varying ratios (1:10–1:100) with purified E-cadherin+ E14.5 cells and reconstituted with embryonic mesenchymal E14.5 cells (E-cadherin–) prior to engraftment.
Variance for all group data is expressed as ± SD. For evaluation of group differences, the unpaired 2-tailed Student’s t test was used assuming equal variance. A P value less than 0.05 was accepted as significant.
This work was supported by the Burroughs Welcome Foundation (to J.P. Alexander) and by NIH grants HL67204 (to H.A. Chapman), HL75680 (to T.H. Vu), and HL73823 (to T.H. Vu). The authors thank Barry Stripp for providing goat anti-CC10 antibodies, Nigel Kileen and Chris Allen (UCSF) for helpful discussions, and Janet Chen and Maria Sereda for technical assistance with the animal colony.
Conflict of interest: The authors have declared that no conflict of interest exists.
Citation for this article: J Clin Invest. 2011;121(7):2855–2862. doi:10.1172/JCI57673.
See the related Commentary beginning on page 2543.