TY - JOUR
T1 - NRG1/ErbB signalling controls the dialogue between macrophages and neural crest-derived cells during zebrafish fin regeneration
AU - Laplace-Builhé, Béryl
AU - Barthelaix, Audrey
AU - Assou, Said
AU - Bohaud, Candice
AU - Pratlong, Marine
AU - Severac, Dany
AU - Tejedor, Gautier
AU - Luz-Crawford, Patricia
AU - Nguyen-Chi, Mai
AU - Mathieu, Marc
AU - Jorgensen, Christian
AU - Djouad, Farida
N1 - Funding Information:
This work was supported by Inserm and University of Montpellier. We thank the MRI facility for their assistance, T. Sauka-Spengler (University of Oxford, United Kingdom) for shipping the Tg(foxd3-mcherry)ct110 zebrafish line, M. Bagnat for shipping Tg(rcn3:gal4/UAS:mCherry) line. A. Kawakami (Tokyo Institute of Technology, Japan) for the junbl plasmid, K. Poss (Duke University Medical Center, USA) for the nrg1 plasmid, R. Kelsh (University of Bath, United Kingdom) for the Fkd6in situ hybridization plasmid. MP and DS acknowledge financial support from the France Génomique National infrastructure, funded as part of “Investissement d’avenir” programme managed by the Agence Nationale pour la Recherche (contract ANR-10-INBS-09). We also thank the Zebrafish facility of the University of Montpellier, the MRI facility for their assistance and the CARTIGEN platform.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/11/3
Y1 - 2021/11/3
N2 - Fish species, such as zebrafish (Danio rerio), can regenerate their appendages after amputation through the formation of a heterogeneous cellular structure named blastema. Here, by combining live imaging of triple transgenic zebrafish embryos and single-cell RNA sequencing we established a detailed cell atlas of the regenerating caudal fin in zebrafish larvae. We confirmed the presence of macrophage subsets that govern zebrafish fin regeneration, and identified a foxd3-positive cell population within the regenerating fin. Genetic depletion of these foxd3-positive neural crest-derived cells (NCdC) showed that they are involved in blastema formation and caudal fin regeneration. Finally, chemical inhibition and transcriptomic analysis demonstrated that these foxd3-positive cells regulate macrophage recruitment and polarization through the NRG1/ErbB pathway. Here, we show the diversity of the cells required for blastema formation, identify a discrete foxd3-positive NCdC population, and reveal the critical function of the NRG1/ErbB pathway in controlling the dialogue between macrophages and NCdC.
AB - Fish species, such as zebrafish (Danio rerio), can regenerate their appendages after amputation through the formation of a heterogeneous cellular structure named blastema. Here, by combining live imaging of triple transgenic zebrafish embryos and single-cell RNA sequencing we established a detailed cell atlas of the regenerating caudal fin in zebrafish larvae. We confirmed the presence of macrophage subsets that govern zebrafish fin regeneration, and identified a foxd3-positive cell population within the regenerating fin. Genetic depletion of these foxd3-positive neural crest-derived cells (NCdC) showed that they are involved in blastema formation and caudal fin regeneration. Finally, chemical inhibition and transcriptomic analysis demonstrated that these foxd3-positive cells regulate macrophage recruitment and polarization through the NRG1/ErbB pathway. Here, we show the diversity of the cells required for blastema formation, identify a discrete foxd3-positive NCdC population, and reveal the critical function of the NRG1/ErbB pathway in controlling the dialogue between macrophages and NCdC.
KW - Animal Fins
KW - Animals
KW - Cell Proliferation
KW - Forkhead Transcription Factors
KW - Gene Expression Regulation, Neoplastic
KW - Developmental; Genes
KW - erbB
KW - Larva
KW - Macrophages
KW - Neural Crest
KW - Neuregulin-1
KW - Regeneration
KW - Signal Transduction
KW - Stem Cells
KW - Zebrafish
KW - Zebrafish Proteins
UR - http://www.scopus.com/inward/record.url?scp=85118570447&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/60d50460-81c1-3752-b42e-3f91d25f77a2/
U2 - 10.1038/s41467-021-26422-5
DO - 10.1038/s41467-021-26422-5
M3 - Article
C2 - 34732706
AN - SCOPUS:85118570447
SN - 2041-1723
VL - 12
SP - 6336
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6336
ER -