4.6 Article

Characterization of Tg(Etv4-GFP) and Etv5RFP Reporter Lines in the Context of Fibroblast Growth Factor 10 Signaling During Mouse Embryonic Lung Development

Journal

FRONTIERS IN GENETICS
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2019.00178

Keywords

ETV4; ETV5; FGF10; lung development; branching morphogenesis

Funding

  1. Deutsche Forschungsgemeinschaft [DFG] [BE4443/1-1, BE4443/4-1, BE4443/6-1, KFO309 P7, SFB1213, EXC2026, 390649896]
  2. Landes-Offensive zur Entwicklung Wissenschaftlich-Okonomischer Exzellenz (LOEWE)
  3. UKGM
  4. Universities of Giessen and Marburg Lung Center (UGMLC)
  5. DZL
  6. COST [BM1201]
  7. University Hospital Giessen and Marburg (UKGM)
  8. German Center for Lung Research (DZL)
  9. National Nature Science Foundation of China [81570075, 81770074, 31471269, 81600062]
  10. Zhejiang Provincial Natural Science Foundation [LZ15H010001, LY18H010006]
  11. Zhejiang Provincial Science Technology Department Foundation [2015103253, 2018264229]
  12. National Key Research and Development Program of China [2016YFC1304000]
  13. Wenzhou public welfare science and technology project [Y20180125]
  14. Scientific research incubation project of the First Affiliated Hospital of Wenzhou Medical University [FHY2015037]

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Members of the PEA3 transcription factors are emerging as bone fide targets for fibroblast growth factor (FGF) signaling. Among them, ETV4 and ETV5 appear to mediate FGF10 signaling during early embryonic lung development. In this paper, recently obtained Tg(Etv4-GFP) and Etv5CreERT2-RFP fluorescent reporter lines were generally characterized during early embryonic development and in the context of FGF10 signaling, in particular. We found that both Tg(Etv4-GFP) and Etv5CreERT2-RFP were primarily expressed in the epithelium of the lung during embryonic development. However, the expression of Etv5CreERT2-RFP was much higher than that of Tg(Etv4-GFP), and continued to increase during development, whereas Tg(Etv4-GFP) decreased. The expression patterns of the surrogate fluorescent protein GFP and RFP for ETV4 and ETV5, respectively, agreed with known regions of FGF10 signaling in various developing organs, including the lung, where ETV4-GFP was seen primarily in the distal epithelium and to a lesser extent in the surrounding mesenchyme. As expected, ETV5-RFP was restricted to the lung epithelium, showing a decreasing expression pattern from distal buds to proximal conducting airways. FGF10 inhibition experiments confirmed that both Etv4 and Etv5 are downstream of FGF10 signaling. Finally, we also validated that both fluorescent reporters responded to FGF10 inhibition in vitro. In conclusion, these two reporter lines appear to be promising tools to monitor FGF10/FGFR2b signaling in early lung development. These tools will have to be further validated at later stages and in other organs of interest.

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