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Pharmacological Microglial Inhibition Remodels the Scar Microenvironment to Support Reticulospinal Circuit Reconstruction After Spinal Cord Injury

Title: Pharmacological Microglial Inhibition Remodels the Scar Microenvironment to Support Reticulospinal Circuit Reconstruction After Spinal Cord Injury
Authors: Run Li; Hongyuan Xing; Yifan Shen; Meng Chen; Bowen Lyu; Xiaofeng Yang; Li Sun; Chao Jiang; Jianyu Lv; Xin Ding; Zhongyang Gao; Yue Wang
Source: Advanced Science, Vol 13, Iss 1, Pp n/a-n/a (2026)
Publisher Information: Wiley
Publication Year: 2026
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: Î22‐adrenergic receptor; microglial inhibition; motor function recovery; reticulospinal tract; spinal cord injury; Science
Description: Due to an inhibitory scar microenvironment that prevents neural circuit reconstruction, spinal cord injury (SCI) often leads to persistent neurological dysfunction. Although neonatal murine models demonstrate that microglial inhibition enables scar remodeling to support neuroregeneration and functional recovery, effective pharmacological suppression of microglial activation in adult SCI remain elusive. Here, this work demonstrates that early β2‐adrenergic receptor agonist treatment drives microglial transition to a homeostatic phenotype within the post‐SCI scar. This intervention reduces inhibitory extracellular matrix deposition and transforms the inhibitory microenvironments into permissive substrates for axonal regrowth. Anatomical analyses reveal regeneration of the reticulospinal tract, which establishes synaptic connectivity with thoracolumbar circuits to mediate motor recovery in a complete SCI. These findings elucidate the therapeutic potential and neural circuit mechanisms underlying pharmacological microglial modulation for SCI repair, establishing a glial‐neural circuit reparative paradigm.
Document Type: article in journal/newspaper
Language: English
Relation: https://doi.org/10.1002/advs.202503966; https://doaj.org/toc/2198-3844; https://doaj.org/article/0339b5fe0e704268b23297a29a1bcf5e
DOI: 10.1002/advs.202503966
Availability: https://doi.org/10.1002/advs.202503966; https://doaj.org/article/0339b5fe0e704268b23297a29a1bcf5e
Accession Number: edsbas.F1A9EECF
Database: BASE