Journalartikel
Autorenliste: Taghizadeh, Sara; Heiner, Monika; Vazquez-Armendariz, Ana Ivonne; Wilhelm, Jochen; Herold, Susanne; Chen, Chengshui; Zhang, Jin San; Bellusci, Saverio
Jahr der Veröffentlichung: 2021
Seiten: 1382-1394
Zeitschrift: Stem Cells
Bandnummer: 39
Heftnummer: 10
ISSN: 1066-5099
eISSN: 1549-4918
Open Access Status: Hybrid
DOI Link: https://doi.org/10.1002/stem.3423
Verlag: Oxford University Press
Abstract:
Resident mesenchymal cells (rMCs defined as Cd31(Neg)Cd45(Neg)Epcam(Neg)) control the proliferation and differentiation of alveolar epithelial type 2 (AT2) stem cells in vitro. The identity of these rMCs is still elusive. Among them, Axin2(Pos) mesenchymal alveolar niche cells (MANCs), which are expressing Fgf7, have been previously described. We propose that an additional population of rMCs, expressing Fgf10 (called rMC-Sca1(Pos)Fgf10(Pos)) are equally important to maintain AT2 stem cell proliferation. The alveolosphere model, based on the AT2-rMC co-culture in growth factor-reduced Matrigel, was used to test the efficiency of different rMC subpopulations isolated by FACS from adult murine lung to sustain the proliferation and differentiation of AT2 stem cells. We demonstrate that rMC-Sca1(Pos)Fgf10(Pos) cells are efficient to promote the proliferation and differentiation of AT2 stem cells. Co-staining of adult lung for Fgf10 mRNA and Sftpc protein respectively, indicate that 28% of Fgf10(Pos) cells are located close to AT2 cells. Co-ISH for Fgf7 and Fgf10 indicate that these two populations do not significantly overlap. Gene arrays comparing rMC-Sca1(Pos)Axin2(Pos) and rMC-Sca1(Pos)Fgf10(Pos) support that these two cell subsets express differential markers. In addition, rMC function is decreased in obese ob/ob mutant compared to WT mice with a much stronger loss of function in males compared to females. In conclusion, rMC-Sca1(Pos)Fgf10(Pos) cells play important role in supporting AT2 stem cells proliferation and differentiation. This result sheds a new light on the subpopulations of rMCs contributing to the AT2 stem cell niche in homeostasis and in the context of pre-existing metabolic diseases.
Zitierstile
Harvard-Zitierstil: Taghizadeh, S., Heiner, M., Vazquez-Armendariz, A., Wilhelm, J., Herold, S., Chen, C., et al. (2021) Characterization in mice of the resident mesenchymal niche maintaining AT2 stem cell proliferation in homeostasis and disease, Stem Cells, 39(10), pp. 1382-1394. https://doi.org/10.1002/stem.3423
APA-Zitierstil: Taghizadeh, S., Heiner, M., Vazquez-Armendariz, A., Wilhelm, J., Herold, S., Chen, C., Zhang, J., & Bellusci, S. (2021). Characterization in mice of the resident mesenchymal niche maintaining AT2 stem cell proliferation in homeostasis and disease. Stem Cells. 39(10), 1382-1394. https://doi.org/10.1002/stem.3423
Schlagwörter
AT2; BRANCHING MORPHOGENESIS; FGF10; LIPOFIBROBLAST; resident mesenchymal niche