TY - JOUR
T1 - TNF signaling and macrophages govern fin regeneration in zebrafish larvae
AU - Nguyen-Chi, Mai
AU - Laplace-Builhé, Béryl
AU - Travnickova, Jana
AU - Luz-Crawford, Patricia
AU - Tejedor, Gautier
AU - Lutfalla, Georges
AU - Kissa, Karima
AU - Jorgensen, Christian
AU - Djouad, Farida
N1 - Publisher Copyright:
© The Author(s) 2017.
PY - 2017/8
Y1 - 2017/8
N2 - Macrophages are essential for appendage regeneration after amputation in regenerative species. The molecular mechanisms through which macrophages orchestrate blastema formation and regeneration are still unclear. Here, we use the genetically tractable and transparent zebrafish larvae to study the functions of polarized macrophage subsets during caudal fin regeneration. After caudal fin amputation, we show an early and transient accumulation of pro-inflammatory macrophages concomitant with the accumulation of non-inflammatory macrophages which, in contrast to pro-inflammatory macrophages, remain associated to the fin until the end of the regeneration. Chemical and genetic depletion of macrophages suggested that early recruited macrophages that express TNFα are critical for blastema formation. Combining parabiosis and morpholino knockdown strategies, we show that TNFα/TNFR1 signaling pathway is required for the fin regeneration. Our study reveals that TNFR1 has a necessary and direct role in blastema cell activation suggesting that macrophage subset balance provides the accurate TNFα signal to prime regeneration in zebrafish.
AB - Macrophages are essential for appendage regeneration after amputation in regenerative species. The molecular mechanisms through which macrophages orchestrate blastema formation and regeneration are still unclear. Here, we use the genetically tractable and transparent zebrafish larvae to study the functions of polarized macrophage subsets during caudal fin regeneration. After caudal fin amputation, we show an early and transient accumulation of pro-inflammatory macrophages concomitant with the accumulation of non-inflammatory macrophages which, in contrast to pro-inflammatory macrophages, remain associated to the fin until the end of the regeneration. Chemical and genetic depletion of macrophages suggested that early recruited macrophages that express TNFα are critical for blastema formation. Combining parabiosis and morpholino knockdown strategies, we show that TNFα/TNFR1 signaling pathway is required for the fin regeneration. Our study reveals that TNFR1 has a necessary and direct role in blastema cell activation suggesting that macrophage subset balance provides the accurate TNFα signal to prime regeneration in zebrafish.
UR - http://www.scopus.com/inward/record.url?scp=85029923779&partnerID=8YFLogxK
U2 - 10.1038/CDDIS.2017.374
DO - 10.1038/CDDIS.2017.374
M3 - Article
C2 - 28796253
AN - SCOPUS:85029923779
SN - 2041-4889
VL - 8
JO - Cell Death and Disease
JF - Cell Death and Disease
IS - 8
M1 - e2979
ER -