TY - JOUR
T1 - Subcellular second messenger networks drive distinct repellent-induced axon behaviors
AU - Baudet, Sarah
AU - Zagar, Yvrick
AU - Roche, Fiona
AU - Gomez-Bravo, Claudia
AU - Couvet, Sandrine
AU - Bécret, Johann
AU - Belle, Morgane
AU - Vougny, Juliette
AU - Uthayasuthan, Sinthuya
AU - Ros, Oriol
AU - Nicol, Xavier
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12/1
Y1 - 2023/12/1
N2 - Second messengers, including cAMP, cGMP and Ca2+ are often placed in an integrating position to combine the extracellular cues that orient growing axons in the developing brain. This view suggests that axon repellents share the same set of cellular messenger signals and that axon attractants evoke opposite cAMP, cGMP and Ca2+ changes. Investigating the confinement of these second messengers in cellular nanodomains, we instead demonstrate that two repellent cues, ephrin-A5 and Slit1, induce spatially segregated signals. These guidance molecules activate subcellular-specific second messenger crosstalk, each signaling network controlling distinct axonal morphology changes in vitro and pathfinding decisions in vivo.
AB - Second messengers, including cAMP, cGMP and Ca2+ are often placed in an integrating position to combine the extracellular cues that orient growing axons in the developing brain. This view suggests that axon repellents share the same set of cellular messenger signals and that axon attractants evoke opposite cAMP, cGMP and Ca2+ changes. Investigating the confinement of these second messengers in cellular nanodomains, we instead demonstrate that two repellent cues, ephrin-A5 and Slit1, induce spatially segregated signals. These guidance molecules activate subcellular-specific second messenger crosstalk, each signaling network controlling distinct axonal morphology changes in vitro and pathfinding decisions in vivo.
U2 - 10.1038/s41467-023-39516-z
DO - 10.1038/s41467-023-39516-z
M3 - Article
C2 - 37369692
AN - SCOPUS:85163736196
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3809
ER -