The epithelium lining the conducting airway and alveolar compartments of the lung play a primary role in gas transport and exchange, respectively. Equally important functions of the epithelium are regulation of host defence and intrinsic reparative capacity following microbial- or xenobiotic-initiated tissue damage. To accomplish these functions, the epithelium of the mammalian lung has evolved a compartmental organization along the proximal–distal axis, distinct regions of which are defined by their unique cellular composition. The normal human tracheal and bronchial epithelium is a pseudostratified epithelium predominantly comprised of basal, ciliated, goblet and serous cells. More distal within intrapulmonary conducting airways is a more simplified columnar epithelium defining the bronchiolar airway epithelium. The bronchiolar epithelium of humans is comprised of ciliated cells, non-ciliated secretory Clara cells and relatively few basal cells and is devoid of goblet cells 1, 2. Conducting airways of the human lung terminate in a transitional zone of respiratory epithelium, referred to as the respiratory bronchiole. Respiratory bronchioles include conducting portions lined by cuboidal bronchiolar epithelium, comprised of Clara and ciliated cells in addition to frequent alveoli that bud from the airway wall.
Despite functional conservation of epithelial compartments between species, their relative size and cellular composition varies. The most dramatic anatomical difference between species is evidenced by the number of intrapulmonary conducting airway branches and the relative abundance of bronchial versus bronchiolar epithelium. Multiple generations of intrapulmonary bronchi observed in humans are limited to one or two generations in mice, in which bronchioles predominate. Moreover, bronchioles in mouse airways make the transition directly into alveolar ducts without the transitional respiratory bronchiolar zone typical of larger mammalian species. Corresponding differences are observed in cell types lining airways of the mouse lung. Basal cells are restricted to the tracheal epithelium, ciliated cell abundance diminishes significantly along the proximal–distal axis, and Clara cells are particularly abundant within bronchiolar airways 3. Cell types of the alveolar epithelium show minimal differences between species (Figure 1).
The complex anatomical organization of these cellular components is regulated by a highly coordinated and stereotypic developmental programme, as assessed by interrogation of mouse models. Lung development initiates following fate specification within the ventral foregut endoderm and can be defined by Nkx2.1 expression 4. Recent data indicate that branching occurs through a combination of three geometric branch types in a combination with three stereotypical series 5. Regulation of cell proliferation and fate are tightly linked to this process, as signalling perturbations impacting these processes lead to a variety of defects in lung branching and specification of epithelial lineages. These signalling events involve reciprocal interactions between epithelial and mesenchymal cell types, resulting in coordinated growth and differentiation. Even though far less is known of signalling axes that contribute to epithelial behaviour in the adult lung, it is clear that the epithelial–mesenchymal signalling axis is retained and its regulation is critical to tissue homeostasis.
Epithelial function: mucociliary clearance and immunoregulation
The complex cellular composition of the airway epithelium provides key defensive properties for the lung (Figure 1). As reviewed extensively by Knowles and Boucher 6, the first line of defence to inhaled particulates, oxidants and biological flora is the airway surface fluid (ASF). The ASF is comprised of the mucus layer, of which the predominant protein components are Muc5ac and Muc5ab, and a subtending periciliary liquid layer (PCL) that provides an unrestricted media for ciliary beating and effective mucus transport. Inhaled microorganisms and environmental stimuli are immediately ensnared in the dense mucus of the ASF, preventing further entry to the more susceptible distal conducting and alveolar compartments. Through precise regulation of PCL height, ciliated cells coordinately regulate mucociliary clearance. Effective mucociliary clearance is estimated to take 6 h, implying that this mechanism alone is not enough to protect from infection 6. As such, the ASF also includes several anti-microbial proteins that inhibit bacterial proliferation to allow for effective removal through mucociliary clearance without infection, thus minimizing the need for a massive inflammatory response 7.
The distal airway epithelial cells, specifically the Clara cell, may also play a prominent role in providing important immunoregulatory properties. The principle secreted protein product of the Clara cell, Clara cell secretory protein (CCSP, Scgb1a1), is also the predominant protein product of ASF and precipitously declines in chronic lung disease 8–12. To study the effects of CCSP deficiency on lung function, mice homozygous null for CCSP (CCSP−/−) were generated 13, 14. Exposure of CCSP−/− mice to pulmonary irritants, pollutants and microbes have revealed that Clara cell secretions can regulate the immunoregulatory aspects of the airway epithelium 15–22. Recent studies in which NF-κB is inhibited or augmented in Clara cells suggests that the LPS elicited inflammatory response is dependent upon signalling in the airway epithelium 23–25. This process is likely initiated by secretion of paracrine signalling molecules from macrophages such as TNFα 26. We have more recently demonstrated that the airway epithelium, through Clara cell secretions, regulates crosstalk with lung macrophages 27. Collectively, these data indicate that airway epithelial specification and effective repair and maintenance are critical for lung homeostasis.
The remainder of this review deals principally with the cellular and molecular mechanisms involved in epithelial maintenance. We place emphasis on defining the putative stem cell hierarchies endogenous to the conducting airway epithelium and their molecular regulators and evaluate their contribution to lung disease.
Defining a stem cell hierarchy
Hierarchical organization of progenitor cells into what is commonly referred to as a ‘stem cell hierarchy’ has classically been described in tissues that display a high rate of cellular turnover, such as the small intestine and skin. Specifically, the intestinal epithelium, as a result of persistent epithelial damage, is continually regenerating, resulting in cellular turnover of approximately 5 days. Tissue stem cells of this hierarchy have been defined using functional assays that interrogate proliferative frequency, self-renewal and differentiation potential 28. Small numbers of intestinal stem cells are thought to reside at or near the base of the intestinal crypt and give rise to a more abundant population of highly proliferative transit-amplifying cells located more proximally within the crypt 29, 30. Transit-amplifying cells of the intestinal epithelium represent an obligate progenitor cell pool lacking differentiated characteristics and are committed to a high rate of proliferation, necessary for the generation of differentiating progeny 31. This strategy for rapid tissue replacement is shared by the skin, in which an obligate transit-amplifying progenitor cell that is both abundant and broadly distributed within the epidermis continuously generates differentiating progeny through a stochastic mechanism 32, 33. In the skin, resting tissue stem cells are maintained in a quiescent state and are only activated to proliferate in response to depletion of the transit-amplifying pool, through a process thought to be highly regulated by calcineruin, BMP and NFATc1 34, 35. The relative quiescence of tissue stem cells in comparison to their more abundant transit-amplifying progeny has become a controversial topic in recent studies investigating intestinal stem cells. However, the property of DNA label retention remains a commonly used assay for the identification and localization of resident tissue stem cells 28.
The epithelium lining pulmonary airways turns over slowly during the normal process of tissue maintenance. Methods used to calculate the rate of epithelial turnover rely on indirect approaches that are based upon measurements of cell proliferation and lineage tagging. Measurements of cell proliferation have principally relied upon stable incorporation of labelled DNA precursors, such as bromodeoxyuridine (BrdU) or [H3]-thymidine, into the DNA of cells traversing S-phase. Using this approach, estimates of the steady-state instantaneous proliferative fraction were determined to be 1.3% in tracheal epithelium 36 and 0.06% in bronchiolar epithelium 37. Data generated from continuous labelling of the steady-state bronchiolar epithelium further demonstrated that the frequency of bronchiolar epithelium is 1%/day 38. Assuming a direct relationship between the rate of epithelial cell loss and replacement, these data suggest that epithelial cells have an average life span of 100 days in bronchioles. Direct measurement of ciliated cell half-life as a measure of epithelial turnover, made by Rawlins and Hogan, indicated that this subpopulation of epithelial cells has an estimated half-life of either 6 or 17 months in trachea and bronchioles, respectively 39. Estimates made using either approach indicate that the epithelium of the trachea turns over more rapidly than that of bronchioles. While both methods are technically flawed, due to the inability to directly assess Clara cell turnover, these studies demonstrate that the frequency with which the airway epithelium turns over is similar to that described for the endocrine pancreas and other foregut-derived tissues 40 but differs significantly from the rapid rate of epithelial turnover observed in tissues derived from hindgut endoderm, such as the small intestine 28. These data suggest fundamental differences in the regulation of progenitor cells between slowly and rapidly replacing tissue 41, 42.
Recent work has called into question the existence of stem cells in slowly renewing tissues 43, 44. As indicated above, the lung epithelium is replaced far more slowly than specialized post-mitotic cell types of either the gut or the epidermis, a property that is reflected in the functional characteristics of airway progenitor cells in resting versus proliferative states. Therefore, it is not surprising that progenitor cell hierarchies of the lung and other slowly renewing tissues do not fit the classical stem cell hierarchies described in tissues of rapid turnover 41. In fact, Hu and colleagues, through use of in vivo injury models, have recently described the existence of a stem cell capable of renewing the endocrine pancreas, a tissue that until recently was thought to be maintained solely through self-duplication of differentiated β cells 45. This, and previous work in lung to be discussed in more detail below, illustrate a deviation from the classical stem cell hierarchy marked by lack of an obligate transit-amplifying progenitor cell in the steady state. Rather, slowly renewing tissues such as lung are maintained at steady state by an abundant facultative transit-amplifying progenitor that fulfils characteristics of a differentiated cell type in the quiescent state, yet retains proliferative capacity and the ability to generate daughter cells capable of generating other specialized lineages. Therefore, the endogenous stem cell at steady-state likely remains quiescent. However, studies utilizing in vivo injury models have revealed stem cells that can be functionally distinguished from facultative progenitors, based upon their resistance to environmental stimuli and spatial localization in the conducting airway (Figure 2). These studies are highlighted in detail below.
Progenitor cells in airway repair: tracheobronchial epithelium
Studies investigating progenitor cells of the tracheobronchial epithelium have benefited from a combination of in vivo, transplantation and in vitro models to reveal contributions made by distinct cell types of the normal epithelium towards maintenance and renewal. In vivo models have used a variety of agents to injure the epithelium, including detergents such as polydocanol 36, toxic gases such as ozone 46, nitrogen dioxide 46, 47 or sulphur dioxide 36, parenterally administered toxicants such as naphthalene 48 and mechanical wounding of the epithelium 49. Using these models, both basal and non-ciliated secretory cells have been shown to exhibit progenitor potential. In this context, the term ‘progenitor cell’ refers to any proliferative cell defined by stable incorporation of [H3]-thymidine into its nuclear DNA. Cell fractionation and retroviral lineage tracing coupled with functional analysis in reconstituted tracheal grafts has allowed detailed analysis of the differentiation potential and clonogenic capacity of these progenitor cells. These approaches have revealed subpopulations of tracheobronchial basal cells that can be distinguished according to their label retention, differentiation potential and clonogenic capacity 36, 50, 51. More recently, related experiments using in vivo lineage-tagging approaches have confirmed results from xenograft experiments and indicate that a subpopulation of cytokeratin 14-expressing cells exhibit both multipotent differentiation potential and significant clonogenic capacity 52, 53. Collectively these data reveal a number of progenitor cell types that contribute to maintenance and repair of the tracheobronchial epithelium, some of which exhibit significant clonogenic potential in vitro or in-tracheal grafts suggestive of the existence of local stem cells.
The observation of a less abundant population of infrequently cycling basal-like cells within intercartilagenous regions of the tracheal epithelium and the ducts of submucosal glands provided the first direct evidence suggesting the existence of stem-like cells within tracheobronchial airways. These cells were found to express high levels of cytokeratin 5 and, when isolated, were greatly enriched for in vitro clone-forming cells. Among the clone-forming cells, approximately 5% had the capacity to generate large clones analogous to highly clonogenic cells observed in vivo and in transplantation experiments 54. These findings reinforce the concept that basal cells are a heterogeneous population that includes abundant transit-amplifying populations in addition to a rare subset of cells with properties of resident tissue stem cells (Figure 2).
Progenitor cells in airway repair: bronchiolar epithelium
Cell type-selective toxicants have been used extensively to reveal progenitor cell types contributing to epithelial repair. Seminal work by Evans and colleagues used oxidant gases allowing selective injury of ciliated cells to demonstrate that the airway epithelium is repaired through a non-ciliated progenitor 46. They went on to demonstrate that proliferating Clara cells lose ultrastructural features typical of the quiescent state, giving rise to a cell type that was termed the type A Clara cell. Based upon this analysis, type A Clara cells were distinguished from their mature quiescent counterparts based upon lack of secretory granules and smooth endoplasmic reticulum, and their ability to incorporate labelled DNA precursors. Type A cells contribute to repair by actively proliferating and differentiating into mature Clara cells and terminally differentiated ciliated cells. These studies identified Clara cells as an abundant facultative transit-amplifying progenitor cell with the capacity for bipotential differentiation and suggested that the normally slow rate of epithelial renewal in the steady state could be dramatically increased in the setting of airway injury 47. Clara cells are analogous to transit-amplifying cells of the gut and epidermis, yet have the important distinction of quiescence and other specialized functions in the steady state, including immunoregulation and xenobiotic metabolism.
The experimental demonstration in airways of an epithelial pool of putative tissue stem cells was made through use of injury models in which the abundant facultative progenitor cell, the Clara cell, was specifically ablated. Clara cells represent one of the principal sites in the lung at which endogenous and xenobiotic lipophilic compounds are metabolized through phase I oxidation reactions, such as those catalysed by cytochrome P450 (CyP450) mono-oxygenases. This function of Clara cells renders them particularly susceptible to chemical injury by xenobiotic chemicals that serve as substrates for members of this class of enzymes, and represents the basis for selective ablation of Clara cells in mice following exposure to naphthalene 55, 56. Use of this injury model in mice allowed identification of two putative stem cell niches in bronchioles based upon the resistance to naphthalene-induced injury and distribution of regenerating epithelial foci containing nascent Clara cells (Figure 2). The first was located predominantly at airway branchpoints found in close proximity to neuro-epithelial bodies (NEBs) 48. NEB-associated regenerative foci harboured two proliferative populations of non-ciliated cells, one expressing Clara cell secretory protein (CCSP) and one expressing the pulmonary neuroendocrine cell (PNEC)-specific marker calcitonin gene-related peptide (CGRP) 37, 57, 58. A second microenvironment contributing to replacement of depleted Clara cells was located in the terminal bronchiolar epithelium adjacent to the bronchioalveolar duct junction (BADJ) 48. Chemically resistant proliferative cells located at the BADJ express the secretory cell marker CCSP and, unlike regenerative foci in more proximal airways, lack a restricted association with PNECs 59.
The critical role played by NEB- and BADJ-associated CCSP-expressing cells in repair of Clara cell-depleted airways was demonstrated using a transgenic mouse model allowing conditional ablation of naphthalene-sensitive and -resistant CCSP-expressing cells. In this model, airway repair was completely abrogated, suggesting that CGRP+ PNECs are not the progenitors of the airway epithelium 38. These studies clearly identified up to three distinct populations of CCSP-expressing cells that are stably maintained within the bronchiole of normal adult mice. Of these populations, rare NEB- and BADJ-associated CCSP-expressing cells share the property of infrequent proliferation relative to their more differentiated Clara cell counterparts 38, 59. Similarities between rare naphthalene-resistant CCSP-expressing cells and tissue stem cells of other organs form the basis for their designation as a putative bronchiolar stem cell that is sometimes referred to as either the variant Clara cell or variant CCSP-expressing cell 38. Further distinctions were made between bronchiolar stem and Clara cells, based upon the observation of rare CCSP-expressing cells that co-express the alveolar type 2 cell marker surfactant protein C (SP-C), that these cells were localized to the BADJ, and that they were resistant to naphthalene. Cells with this molecular phenotype were observed in preparations of distal airway/alveolar epithelial cells and could be enriched from this crude cell preparation based upon their unique expression of stem cell antigen-1 (Sca-1) and CD34. The observation that in vitro culture of these cells resulted in the expression of aquaporin 5, a gene commonly associated with type 1 alveolar epithleial cells, led to the conclusion that they harboured the capacity for both bronchiolar and alveolar differentiation and formed the basis for their designation as bronchioalveolar stem cells (BASCs) 60.
At the time of this review, no in vivo data directly demonstrate that a BADJ-associated CCSP-expressing population has the capacity for bronchiolar and alveolar differentiation. As such, the similarity between variant Clara cells and BASCs has not been established. Moreover, recent studies investigating the cell surface phenotype of epithelial cells from mouse conducting airways indicate that, although cell surface Sca-1 allows for discrimination of conducting airway and alveolar epithelial cells, it does not distinguish the local stem cell population residing within distal bronchioles from the more abundant population of Clara cells 61.
Molecular regulation of the lung stem cell hierarchy
Investigation into mechanisms regulating the airway stem cell hierarchy have focused predominantly on genetic manipulation of candidate signalling pathways and molecules with established roles as regulators of lung development or carcinogenesis. These include canonical Wnt signalling through stabilization of β-catenin, signalling through either the MAP kinase or Ras pathways, PTEN, GATA-6 and Bmi1. These studies have typically relied upon knock-out, ectopic expression strategies or the use of conditional gene manipulation approaches that led to altered expression of key regulatory molecules. Ectopic activation of β-catenin signalling, K-Ras signalling or developmental loss of either GATA-6, PTEN, PI3 kinase or p38α MAP kinase, have all been found to result in increases in the abundance of CCSP/Pro-SPC dual immunopositive cells that are believed to represent bronchiolar stem cells 60, 62–68.
Changes in the pool size of bronchiolar progenitor cells have been investigated in many of these models through analysis of the cell surface phenotype described by Kim and co-workers, including Sca-1+/CD34+ cells within the CD45−/CD31− viable fraction of dissociated lung cells 60. However, even though changes in these signalling pathways result in the expansion of putative stem cells based upon the use of these markers, the absence of a comprehensive molecular phenotype for bronchiolar stem cells that distinguishes them from other airway progenitor cell types suggests that the impact of altered signalling on stem cells per se can not easily be determined. In this context, functional changes in epithelial repair capacity involving use of injury models that are known to result in activation of putative stem cells has the potential to provide a more direct means to interrogate changes in progenitor function.
Roles for progenitor cells in carcinogenesis
Cancers in the lung can be pathologically divided into two categories, based upon the initiating cell type, tumour location and histopathology, and are termed ‘small cell lung cancers’ (SCLCs) and ‘non-small cell lung cancers’ (NSCLCs). NSCLCs can be further divided into squamous cell carcinoma (SCC), adenocarcinoma (AC), and large cell carcinoma (LCC) 69. As reviewed extensively by Giangreco and Janes, the varying tumour types present is a representation of the complex cellular compartmentalization in the lung 70. Using a similar strategy to that of Bonnet and Dick 71, Eramo and co-workers recently demonstrated that human lung tumours can be fractionated based upon cell surface expression of CD133+, and demonstrate that CD133+ tumour cells can self-renew and propagate tumours in SCID mice, while CD133− cells do not 72. These data have been used in support of the popular concept that tumours, much like normal tissues, are maintained by rare cancer stem cells and are the only studies currently to adequately demonstrate that a cancer stem cell may exist in lung.
Despite the lack of unequivocal data demonstrating the existence of lung cancer stem cell, a wide body of work exists studying the molecular mechanisms of lung carcinogenesis in bronchiolar progenitor cells. Many of these studies have stemmed from the finding that an important gene frequently mutated in human lung cancer is K-ras73. While there is a large body of evidence that establishes the cause–effect relationship between k-ras and lung cancer, very few data exist that suggest a direct link between k-ras mutations and the cancer-initiating cell or the cancer stem cell. Studies by Jacks and colleagues have demonstrated that Cre-induced activation of a K-rasLSL allele increases the abundance of CCSP/Pro-SPC dual positive bronchiolar cells (or BASCs) that are found at the bronchioalveolar duct junction. Activation of K-ras signalling in this manner also led to the development of adenocarcinomas, with the suggestion of a causal relationship between increased numbers of BASCs and the development of lung cancer 60. This study has subsequently been followed by several that have attempted to understand alternative molecular mechanisms of tumour initiation, the approach being to manipulate signalling pathways to define those that impact the behaviour of BASCs. Specifically, conditional deletion of PTEN, PI3 kinase or p38α MAP kinase results in increased numbers of BASCs and increased propensity to lung tumour development 64, 66, 68. In contrast, deletion of Bmi1 inhibits tumourigenesis through inhibition of BASC expansion 67. Collectively, these studies have been interpreted to suggest a role for bronchiolar stem cells in the initiation of tumourigenesis. However, these studies either fail to identify the initial target cell within which signalling is disrupted, leading to changes in the behaviour of putative stem cells or other epithelial progenitor cell types of the airway. Therefore, although the concept of a cancer stem cell remains an attractive hypothesis, the relationships between tumour-initiating cells, cancer stem cells and endogenous stem or progenitor cells have yet to be clearly determined in the lung.
Roles for progenitor cells in chronic lung disease
Chronic lung diseases (CLD), such as obliterative bronchiolitis (OB), chronic obstructive pulmonary disease (COPD) and asthma, are characterized by remarkable epithelial and mesenchymal remodelling that includes, but is not limited to, chronic injury to the airway epithelium, decreased abundance of Clara cells, goblet cell hyperplasia, mucus cell metaplasia, subepithelial basement membrane thickening, fibrotic nodules causing stenosis of small airways, airway smooth muscle hypertrophy, and uncontrolled lymphocytic, neutrophilic and monocytic inflammation 74–77. Accordingly, understanding the aetiology and progression of CLD has been complicated, due to the complex network of cellular crosstalk present in the lung. Defective airway epithelial repair has been proposed as an early event in the initiation of CLD, and chronic defects in reparative capacity and cellular composition may further contribute to disease progression and susceptibility to exacerbation 78. This implies that normal functions for facultative progenitor and stem cells are compromised. Evidence suggesting that this may be the case comes from analysis of biomarkers of epithelial remodelling that have been used to follow the severity and progression of lung disease. Levels of CCSP/CC16 in airway lining fluid or serum are uniformly reduced in the setting of chronic lung disease, as discussed above, suggesting that epithelial remodelling involves altered differentiation or cell death of this critical bronchiolar progenitor. Increasing evidence from studies in humans and animal models suggests that chronic injury and inflammation inhibits normal epithelial repair and differentiation, leading to remodelling of the entire epithelial mesenchymal trophic unit (EMTU) 77.
Chronic exposure to xenobiotic and biological flora has been postulated to play a causative role in the development and exacerbation of chronic lung disease. As an example, cigarette smoke causes extensive airway epithelial injury, a robust inflammatory response in the lung, and is the principal epigenetic factor contributing to the development of chronic obstructive pulmonary disease 79. In vitro studies have demonstrated that cigarette smoke can severely blunt epithelial wound repair by decreasing the rate of cell proliferation and migration and altering extracellular matrix remodelling 80. This observation has been extended to in vivo models in which chronic cigarette smoke exposure in mice was shown to attenuate epithelial repair following naphthalene-induced airway injury 81. Epithelial cell injury and persistent inflammation that are both associated with cigarette smoking have also been demonstrated to blunt tissue repair in models of epidermal wound healing 82. These studies indicate that proper epithelial repair can be severely attenuated by environmental challenge.
Mechanisms contributing to tissue remodelling involve changes in the abundance and activity of key matrix remodelling enzymes, leading to excessive depletion of elastin and other structural matrix components critical for maintenance of tissue architecture. Paradoxically, tissue remodelling also includes fibroproliferative responses that lead to inappropriate deposition of matrix molecules. Currently, little is known regarding the cellular crosstalk between injured and repairing epithelium and the underlying mesenchyme. It has been postulated that the EMTU signalling network is essential for proper epithelial repair and that in the context of defective repair this may lead to aberrant and chronic mesenchymal remodelling that includes extensive fibroproliferation, extracellular matrix (EMC) deposition and development of fibrosis. Recent work has identified that ECM production is transiently up-regulated in an in vivo model of productive airway epithelial repair. Specifically, the ECM protein Tenascin C (Tnc) is deposited in the subepithethial mesenchyme, reorganized to the basement membrane subtending regenerating and injured epithelium as repair initiates, and degraded to restore steady-state levels at the return of tissue homeostasis. In contrast, this process is severely deregulated in an in vivo model of defective airway epithelial repair. Irreversible ablation of CCSP-expressing cells using a transgenic suicide gene resulted in chronic ECM deposition subtending the airway epithelium. Surprisingly, defective airway epithelial repair also resulted in over-production of ECM in the alveolar compartment 83. This study further supports work demonstrating that defective airway epithelial repair can also lead to secondary effects in the alveolar compartment, including type 2 cell injury 84. Collectively, these data support an EMTU model in which epithelial repair results in mesenchymal remodelling. This may play a direct role in regulating epithelial proliferation, differentiation and/or migration. After repair is completed, the underlying mesenchyme returns to the steady state. However, in the context of defective epithelial repair or persistent injury, as identified in obliterative bronchiolitis, COPD and cystic fibrosis, the mesenchyme is chronically remodelled, resulting in uncontrolled fibroproliferation, ECM deposition, fibrosis and impaired gas transport/exchange in the airway and alveolar epithelium, respectively (Figure 2C). Further studies are warranted to elucidate the molecular mechanisms regulating this process.
Maintenance of the airway epithelium through the action of multiple interdependent regenerative zones suggests that a more thorough understanding of progenitor cell types and their behaviour in normal and diseased states may yield important insights into disease pathophysiology. Examples of basic biological questions that have potential to shed light on mechanisms of normal maintenance, repair and aberrant tissue remodelling include:
1.Basic studies to define the behaviour of airway progenitor cells in normal and diseased states. Epithelial maintenance is dependent upon a balance between turnover and renewal. If the rate of epithelial turnover is held constant, maintenance is purely a function of progenitor cell self-renewal versus differentiation. There is currently no information in the existing literature that describes the probability with which different progenitor cell types are maintained through self-renewal, or whether this property is impacted by divergence from the steady state, such as might be the case with acute or chronic lung disease. The existence of multiple progenitor cell types that can be hierarchically organized, such as those of the bronchiolar epithelium, increase the complexity of this question. It is possible, for example, that bronchiolar stem cells are maintained through a highly regulated process involving extrinsic signals from the stem cell niche to ensure long-term maintenance of a stem cell pool of a defined size. The likelihood that stem cells are activated to participate in epithelial maintenance would inevitably be related to longevity of the transit-amplifying progenitor cell pool. For example, if TA cell maintenance occurs through a stochastic mechanism, as proposed by Jones and co-workers 32, 33, the probability of which is influenced by extrinsic factors such as injury and/or inflammation, the contribution of stem cells towards epithelial maintenance will be strongly influenced by disease. Understanding the basic behaviour of progenitor cells and how this is impacted by disease would provide novel insights into disease pathogenesis and reveal new therapeutic targets that may allow modification of disease outcome.
2.Improved molecular definition of progenitor cell types and their response to injury and repair. A key component of future studies will be to interrogate the molecular profile of stem cells. Previous studies have identified a broader repertoire of molecular markers for identification and analysis of bronchiolar progenitor cells 85. Furthermore, bronchioalveolar stem cells (BASCs) were recently isolated and sorted, based upon their Sca-1+CD45−CD31−CD34+ immunophenotype 60. However, recent cytometric analysis in combination with mouse models suggests these markers do not distinguish putative stem cells from the abundant pool of Clara cells (Teisanu et al, submitted). Previous attempts to isolate airway epithelial stem cells also included enrichment based upon the ability to efflux the DNA dye Hoechst 33 342 dye 86, but recent data indicate that this does not result in significant enrichment 87. Collectively, these data demonstrate that the use of stem cell properties from other tissues to fractionate airway epithelial stem cells is not a valid approach. Rather, new markers, preferably those that identify a novel cell surface phenotype, will need to be identified, using a combination of techniques including cellular fractionation and microarray analysis.
3.Development of in vitro culture models to investigate the behaviour and regulation of stem cells. A common functional assessment of stem cell character is determination of self-renewal and differentiation capacity in vitro. Isolated BASCs have been cultured and shown to demonstrate both of these qualities in vitro60. However, caveats associated with this assay result preclude appropriate assessment of stem cell behaviour. A more appropriate endpoint would be the coupling of in vitro methods for propagation of progenitor cell types with development of transplantation assays, analogous to those used for functional testing of cells of the haematopoietic lineage to assess the behaviour of these cells in vivo88, 89.
4.Comparative stem/progenitor cell biology between mammalian species. A major shortfall of current studies is the lack of correlative human data. In order to develop successful cell and molecular therapeutics that translates into the clinic, stem cells in human airway epithelium need to be identified. Comparative studies aimed at revealing similarities and differences in epithelial maintenance between species will provide valuable information relating to the predictive ability of animal models of human disease.
The existence of endogenous lung epithelial stem cells remains a controversial issue. To facilitate a more thorough understanding of progenitor cell behaviour and the putative stem cell hierarchy will require development of novel endpoints to answer the fundamental questions outlined above. These studies will bring the scientific community one step closer to the development of cellular and molecular strategies for the therapeutic treatment of lung disease.
Supported by NIH Grant Nos ES008964, HL064888 and HL090146.
Power Point slides of the figures from this Review may be found in the supporting information.