3D Cell Culture Models Demonstrate a Role for FGF and WNT Signaling in Regulation of Lung Epithelial Cell Fate and Morphogenesis

. 2020 ; 8 () : 574. [epub] 20200721

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid32850782

FGF signaling plays an essential role in lung development, homeostasis, and regeneration. We employed mouse 3D cell culture models and imaging to study ex vivo the role of FGF ligands and the interplay of FGF signaling with epithelial growth factor (EGF) and WNT signaling pathways in lung epithelial morphogenesis and differentiation. In non-adherent conditions, FGF signaling promoted formation of lungospheres from lung epithelial stem/progenitor cells (LSPCs). Ultrastructural and immunohistochemical analyses showed that LSPCs produced more differentiated lung cell progeny. In a 3D extracellular matrix, FGF2, FGF7, FGF9, and FGF10 promoted lung organoid formation. FGF9 showed reduced capacity to promote lung organoid formation, suggesting that FGF9 has a reduced ability to sustain LSPC survival and/or initial divisions. FGF7 and FGF10 produced bigger organoids and induced organoid branching with higher frequency than FGF2 or FGF9. Higher FGF concentration and/or the use of FGF2 with increased stability and affinity to FGF receptors both increased lung organoid and lungosphere formation efficiency, respectively, suggesting that the level of FGF signaling is a crucial driver of LSPC survival and differentiation, and also lung epithelial morphogenesis. EGF signaling played a supportive but non-essential role in FGF-induced lung organoid formation. Analysis of tissue architecture and cell type composition confirmed that the lung organoids contained alveolar-like regions with cells expressing alveolar type I and type II cell markers, as well as airway-like structures with club cells and ciliated cells. FGF ligands showed differences in promoting distinct lung epithelial cell types. FGF9 was a potent inducer of more proximal cell types, including ciliated and basal cells. FGF7 and FGF10 directed the differentiation toward distal lung lineages. WNT signaling enhanced the efficiency of lung organoid formation, but in the absence of FGF10 signaling, the organoids displayed limited branching and less differentiated phenotype. In summary, we present lung 3D cell culture models as useful tools to study the role and interplay of signaling pathways in postnatal lung development and homeostasis, and we reveal distinct roles for FGF ligands in regulation of mouse lung morphogenesis and differentiation ex vivo.

Zobrazit více v PubMed

Barkauskas C. E., Chung M.-I., Fioret B., Gao X., Katsura H., Hogan B. L. M. (2017). Lung organoids: current uses and future promise. PubMed DOI PMC

Barkauskas C. E., Cronce M. J., Rackley C. R., Bowie E. J., Keene D. R., Stripp B. R., et al. (2013). Type 2 alveolar cells are stem cells in adult lung. PubMed DOI PMC

Bhavanasi D., Klein P. S. (2016). Wnt signaling in normal and malignant stem cells. PubMed DOI PMC

Cardoso W. V., Itoh A., Nogawa H., Mason I., Brody J. S. (1997). FGF-1 and FGF-7 induce distinct patterns of growth and differentiation in embryonic lung epithelium. PubMed DOI

Cardoso W. V., Lü J. (2006). Regulation of early lung morphogenesis: questions, facts and controversies. PubMed DOI

Chen H., Matsumoto K., Brockway B. L., Rackley C. R., Liang J., Lee J.-H., et al. (2012). Airway epithelial progenitors are region specific and show differential responses to bleomycin-induced lung injury. PubMed DOI PMC

Clevers H., Loh K. M., Nusse R. (2014). An integral program for tissue renewal and regeneration: Wnt signaling and stem cell control. PubMed DOI

Colvin J. S., White A. C., Pratt S. J., Ornitz D. M. (2001). Lung hypoplasia and neonatal death in Fgf9-null mice identify this gene as an essential regulator of lung mesenchyme. PubMed

De Arcangelis A., Georges-Labouesse E. (2000). Integrin and ECM functions: roles in vertebrate development. PubMed DOI

De Moerlooze L., Spencer-Dene B., Revest J. M., Hajihosseini M., Rosewell I., Dickson C. (2000). An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.

del Moral P.-M., De Langhe S. P., Sala F. G., Veltmaat J. M., Tefft D., Wang K., et al. (2006). Differential role of FGF9 on epithelium and mesenchyme in mouse embryonic lung. PubMed DOI

Dessimoz J., Opoka R., Kordich J. J., Grapin-Botton A., Wells J. M. (2006). FGF signaling is necessary for establishing gut tube domains along the anterior-posterior axis in vivo. PubMed DOI

Dvorak P., Bednar D., Vanacek P., Balek L., Eiselleova L., Stepankova V., et al. (2018). Computer-assisted engineering of hyperstable fibroblast growth factor 2. PubMed DOI

Frank D. B., Peng T., Zepp J., Snitow M., Vincent T., Penkala I. J., et al. (2016). Emergence of a wave of Wnt signaling that regulates lung alveologenesis through controlling epithelial self-renewal and differentiation. PubMed DOI PMC

Fuchs E., Chen T. (2013). A matter of life and death: self-renewal in stem cells. PubMed DOI PMC

Goss A. M., Tian Y., Tsukiyama T., Cohen E. D., Zhou D., Lu M. M., et al. (2009). Wnt2/2b and beta-catenin signaling are necessary and sufficient to specify lung progenitors in the foregut. PubMed DOI PMC

Guo L., Degenstein L., Fuchs E. (1996). Keratinocyte growth factor is required for hair development but not for wound healing. PubMed DOI

Han R. N., Liu J., Tanswell A. K., Post M. (1992). Expression of basic fibroblast growth factor and receptor: immunolocalization studies in developing rat fetal lung. PubMed DOI

Hegab A. E., Arai D., Gao J., Kuroda A., Yasuda H., Ishii M., et al. (2015). Mimicking the niche of lung epithelial stem cells and characterization of several effectors of their in vitro behavior. PubMed DOI

Jones M. R., Dilai S., Lingampally A., Chao C.-M., Danopoulos S., Carraro G., et al. (2019). A comprehensive analysis of fibroblast growth factor receptor 2b signaling on epithelial tip progenitor cells during early mouse lung branching morphogenesis. PubMed DOI PMC

Kheradmand F., Rishi K., Werb Z. (2002). Signaling through the EGF receptor controls lung morphogenesis in part by regulating MT1-MMP-mediated activation of gelatinase A/MMP2. PubMed PMC

Koledova Z., Sumbal J., Rabata A., de La Bourdonnaye G., Chaloupkova R., Hrdlickova B., et al. (2019). Fibroblast growth factor 2 protein stability provides decreased dependence on heparin for induction of FGFR signaling and alters ERK signaling dynamics. PubMed DOI PMC

Lebeche D., Malpel S., Cardoso W. V. (1999). Fibroblast growth factor interactions in the developing lung. PubMed DOI

Lee J.-H., Bhang D. H., Beede A., Huang T. L., Stripp B. R., Bloch K. D., et al. (2014). Lung stem cell differentiation in mice directed by endothelial cells via a BMP4-NFATc1-Thrombospondin-1 axis. PubMed DOI PMC

Lee J.-H., Tammela T., Hofree M., Choi J., Marjanovic N. D., Han S., et al. (2017). Anatomically and functionally distinct lung mesenchymal populations marked by Lgr5 and Lgr6. PubMed DOI PMC

Lu M. M., Yang H., Zhang L., Shu W., Blair D. G., Morrisey E. E. (2001). The bone morphogenic protein antagonist gremlin regulates proximal-distal patterning of the lung. PubMed DOI

Malpel S., Mendelsohn C., Cardoso W. V. (2000). Regulation of retinoic acid signaling during lung morphogenesis. PubMed

Matsui R., Brody J. S., Yu Q. (1999). FGF-2 induces surfactant protein gene expression in foetal rat lung epithelial cells through a MAPK-independent pathway. PubMed DOI

McQualter J. L., Bertoncello I. (2015). “Clonal culture of adult mouse lung epithelial stem/progenitor cells,” in PubMed DOI

McQualter J. L., Yuen K., Williams B., Bertoncello I. (2010). Evidence of an epithelial stem/progenitor cell hierarchy in the adult mouse lung. PubMed DOI PMC

Miller L.-A. D., Wert S. E., Clark J. C., Xu Y., Perl A.-K. T., Whitsett J. A. (2004). Role of Sonic hedgehog in patterning of tracheal-bronchial cartilage and the peripheral lung. PubMed DOI

Min H., Danilenko D. M., Scully S. A., Bolon B., Ring B. D., Tarpley J. E., et al. (1998). Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to PubMed DOI PMC

Mucenski M. L., Wert S. E., Nation J. M., Loudy D. E., Huelsken J., Birchmeier W., et al. (2003). beta-Catenin is required for specification of proximal/distal cell fate during lung morphogenesis. PubMed DOI

Nyeng P., Norgaard G. A., Kobberup S., Jensen J. (2008). FGF10 maintains distal lung bud epithelium and excessive signaling leads to progenitor state arrest, distalization, and goblet cell metaplasia. PubMed DOI PMC

Ohuchi H., Hori Y., Yamasaki M., Harada H., Sekine K., Kato S., et al. (2000). FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development. PubMed DOI

Pastrana E., Silva-Vargas V., Doetsch F. (2011). Eyes wide open: a critical review of sphere-formation as an assay for stem cells. PubMed DOI PMC

Powell P. P., Wang C. C., Horinouchi H., Shepherd K., Jacobson M., Lipson M., et al. (1998). Differential expression of fibroblast growth factor receptors 1 to 4 and ligand genes in late fetal and early postnatal rat lung. PubMed DOI

Rabata A., Hampl A., Koledova Z. (2017). “Lungosphere assay: 3D culture of lung epithelial stem/progenitor cells,” in PubMed DOI

Ramasamy S. K., Mailleux A. A., Gupte V. V., Mata F., Sala F. G., Veltmaat J. M., et al. (2007). Fgf10 dosage is critical for the amplification of epithelial cell progenitors and for the formation of multiple mesenchymal lineages during lung development. PubMed DOI PMC

Reynolds B. A., Weiss S. (1992). Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system. PubMed DOI

Sekine K., Ohuchi H., Fujiwara M., Yamasaki M., Yoshizawa T., Sato T., et al. (1999). Fgf10 is essential for limb and lung formation. PubMed DOI

Shaw F. L., Harrison H., Spence K., Ablett M. P., Simões B. M., Farnie G., et al. (2012). A detailed mammosphere assay protocol for the quantification of breast stem cell activity. PubMed DOI

Shu W., Guttentag S., Wang Z., Andl T., Ballard P., Lu M. M., et al. (2005). Wnt/β-catenin signaling acts upstream of N-myc, BMP4, and FGF signaling to regulate proximal–distal patterning in the lung. PubMed DOI

Sugimoto S., Sato T. (2017). “Establishment of 3D intestinal organoid cultures from intestinal stem cells,” in PubMed DOI

Tichelaar J. W., Lu W., Whitsett J. A. (2000). Conditional expression of fibroblast growth factor-7 in the developing and mature lung. PubMed DOI

Volckaert T., Campbell A., Dill E., Li C., Minoo P., De Langhe S. (2013). Localized Fgf10 expression is not required for lung branching morphogenesis but prevents differentiation of epithelial progenitors. PubMed DOI PMC

Volckaert T., De Langhe S. P. (2015). Wnt and FGF mediated epithelial mesenchymal crosstalk during lung development. PubMed DOI PMC

Volckaert T., Yuan T., Chao C.-M., Bell H., Sitaula A., Szimmtenings L., et al. (2017). Fgf10-hippo epithelial-mesenchymal crosstalk maintains and recruits lung basal stem cells. PubMed DOI PMC

Volckaert T., Yuan T., Yuan J., Boateng E., Hopkins S., Zhang J.-S., et al. (2019). Hippo signaling promotes lung epithelial lineage commitment by curbing Fgf10 and β-catenin signaling. PubMed DOI PMC

Weaver M., Yingling J. M., Dunn N. R., Bellusci S., Hogan B. L. (1999). Bmp signaling regulates proximal-distal differentiation of endoderm in mouse lung development. PubMed

Wells J. M., Melton D. A. (2000). Early mouse endoderm is patterned by soluble factors from adjacent germ layers. PubMed

White A. C., Xu J., Yin Y., Smith C., Schmid G., Ornitz D. M. (2006). FGF9 and SHH signaling coordinate lung growth and development through regulation of distinct mesenchymal domains. PubMed DOI

Whyte J. L., Smith A. A., Helms J. A. (2012). Wnt signaling and injury repair. PubMed DOI PMC

Yin Y., White A. C., Huh S.-H., Hilton M. J., Kanazawa H., Long F., et al. (2008). An FGF–WNT gene regulatory network controls lung mesenchyme development. PubMed DOI PMC

Yuan T., Volckaert T., Redente E. F., Hopkins S., Klinkhammer K., Wasnick R., et al. (2019). FGF10-FGFR2B signaling generates basal cells and drives alveolar epithelial regeneration by bronchial epithelial stem cells after lung injury. PubMed DOI PMC

Zhao C., Setrerrahmane S., Xu H. (2015). Enrichment and characterization of cancer stem cells from a human non-small cell lung cancer cell line. PubMed DOI

Zhou M., Sutliff R. L., Paul R. J., Lorenz J. N., Hoying J. B., Haudenschild C. C., et al. (1998). Fibroblast growth factor 2 control of vascular tone. PubMed DOI PMC

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Lung Organoids-The Ultimate Tool to Dissect Pulmonary Diseases?

. 2022 ; 10 () : 899368. [epub] 20220713

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...