An axon-intrinsic loop restricts nerve regeneration through axonal protein synthesis

ABSTRACT Injured axons synthesize the RNA Binding Protein KHSRP that promotes mRNA decay and slows nerve regeneration. Axotomy-induced increase in axoplasmic Ca 2+ activates axonal Khsrp translation, and while Ca 2+ returns to pre-injury levels within 16 hours post-axotomy, axonal KHSRP remains elevated. Alternating translation of Reg3a and Khsrp sustains axonal KHSRP levels in regenerating axons. Nerve injury activates Reg3a expression, resulting in increased REG3A synthesis and secretion from axons. REG3A stimulates ER Ca 2+ release to activate PERK, increase eIF2 α phosphorylation, and increase Khsrp translation. Axoplasmic Ca 2+ slowly oscillates in growth cones and Reg3A depletion attenuates growth cone Ca 2+ oscillations, decreases KHSRP synthesis, reduces the axon’s retractive events, and accelerates peripheral nerve regeneration. Thus, REG3A to KHSRP signaling provides an axon-intrinsic loop that decelerates axon growth through localized mRNA translation.

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Publication Details

Journal
Science Advances
Published
2026-08-26
DOI
https://doi.org/10.1126/sciadv.aed0049
Primary Topic
Nerve injury and regeneration
Type
article
Field-Weighted Citation Impact
0.00

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article

An axon-intrinsic loop restricts nerve regeneration through axonal protein synthesis

Ashley L. Kalinski, Courtney N. Buchanan, Elizabeth Thames, Kristy Welshhans et al.
Science Advances
Nerve injury and regeneration
article

An axon-intrinsic loop restricts nerve regeneration through axonal protein synthesis

Ashley L. Kalinski, Courtney N. Buchanan, Elizabeth Thames, Kristy Welshhans, Nora I. Perrone‐Bizzozero, Jordan A. Headen, Irene Dalla Costa, Terika P. Smith, Jeffery L. Twiss, Moira Lopez De Leon, Samaneh Matoo, Lauren S. Vaughn, Molly Conway, Jinyoung Lee, Marie-Claire Honoree, Ansley McKay, Cailyn Tosadori, Lillian F. Thompson
article en

Abstract

ABSTRACT Injured axons synthesize the RNA Binding Protein KHSRP that promotes mRNA decay and slows nerve regeneration. Axotomy-induced increase in axoplasmic Ca 2+ activates axonal Khsrp translation, and while Ca 2+ returns to pre-injury levels within 16 hours post-axotomy, axonal KHSRP remains elevated. Alternating translation of Reg3a and Khsrp sustains axonal KHSRP levels in regenerating axons. Nerve injury activates Reg3a expression, resulting in increased REG3A synthesis and secretion from axons. REG3A stimulates ER Ca 2+ release to activate PERK, increase eIF2 α phosphorylation, and increase Khsrp translation. Axoplasmic Ca 2+ slowly oscillates in growth cones and Reg3A depletion attenuates growth cone Ca 2+ oscillations, decreases KHSRP synthesis, reduces the axon’s retractive events, and accelerates peripheral nerve regeneration. Thus, REG3A to KHSRP signaling provides an axon-intrinsic loop that decelerates axon growth through localized mRNA translation.

Science AdvancesVol. 12(35)
University of South Carolina (US), University of New Mexico (US), NeuroDevelopment Center (US), University of Virginia (US), Center for Autism and Related Disorders (US)
Dr. Miriam and Sheldon G. Adelson Medical Research Foundation, University of South Carolina, National Institutes of Health
Openalex Percentile: Top 99%
Nerve injury and regeneration
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