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Updated: Mar 19, 2026

Using Microfluidics Chips for Live Imaging and Study of Injury Responses in Drosophila Larvae
Published on: February 7, 2014
An evolutionarily conserved mechanism for cAMP elicited axonal regeneration involves direct activation of the dual
Yan Hao1, Erin Frey2, Choya Yoon3
1Department of Molecular Cellular and Developmental Biology, University of Michigan, Ann Arbor, United States.
Abstract:
A broadly known method to stimulate the growth potential of axons is to elevate intracellular levels of cAMP, however the cellular pathway(s) that mediate this are not known. Here we identify the Dual Leucine-zipper Kinase (DLK, Wnd in Drosophila) as a critical target and effector of cAMP in injured axons. DLK/Wnd is thought to function as an injury 'sensor', as it becomes activated after axonal damage. Our findings in both Drosophila and mammalian neurons indicate that the cAMP effector kinase PKA is a conserved and direct upstream activator of Wnd/DLK. PKA is required for the induction of Wnd signaling in injured axons, and DLK is essential for the regenerative effects of cAMP in mammalian DRG neurons. These findings link two important mediators of responses to axonal injury, DLK/Wnd and cAMP/PKA, into a unified and evolutionarily conserved molecular pathway for stimulating the regenerative potential of injured axons.
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