IGFBP5 knockdown is associated with improved early neurovascular regeneration after sciatic nerve injury
Abstract
Peripheral nerve injury (PNI) disrupts neurovascular integrity and leads to persistent sensory and motor dysfunction. Insulin-like growth factor binding protein 5 (IGFBP5) regulates insulin-like growth factor bioavailability and has also been implicated in apoptosis, fibrosis, and extracellular matrix remodeling; however, its role in peripheral nerve regeneration remains unclear. This study investigated the temporal expression pattern of IGFBP5 following sciatic nerve injury (SNI) and examined whether its suppression is associated with early neurovascular regenerative responses. A murine SNI model was established, and IGFBP5 was silenced using perineural delivery of lentiviral short hairpin RNA. Neurovascular remodeling, cellular responses, and stress-related changes were evaluated at 5 days post-injury, and functional recovery was assessed longitudinally up to 12 weeks. We observed that IGFBP5 expression was markedly increased in both proximal and distal nerve segments after injury. IGFBP5 knockdown was associated with increased endothelial and axonal marker signals, accompanied by enhanced Schwann cell– and macrophage-associated responses and reduced myelin-associated signals. In parallel, reduced oxidative and nitrosative stress and decreased apoptotic markers were detected, together with increased proliferative activity during the early phase of regeneration. In addition, IGFBP5 suppression was associated with increased phosphorylation of PI3K–AKT and ERK signaling pathways. Functional assessments indicated improved motor recovery and higher sciatic functional index scores compared with controls. Together, these findings suggest that IGFBP5 knockdown is associated with a more favorable early neurovascular microenvironment following peripheral nerve injury. Targeting IGFBP5 may represent a potential strategy to modulate early regenerative processes, although further studies are required to define its mechanistic role and long-term effects.
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BibTeX
@article{ock2026igfbp5,
title = {{IGFBP5 knockdown is associated with improved early neurovascular regeneration after sciatic nerve injury}},
author = {Jiyeon Ock and Woo Jean Kim and Yan Huang and Fitri Rahma Fridayana and Seongju Lee and Guo Nan Yin and Ji-Kan Ryu},
journal = {Scientific Reports},
year = {2026},
month = oct,
doi = {10.1038/s41598-026-76434-8},
url = {https://www.nature.com/articles/s41598-026-76434-8},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - IGFBP5 knockdown is associated with improved early neurovascular regeneration after sciatic nerve injury
AU - Jiyeon Ock
AU - Woo Jean Kim
AU - Yan Huang
AU - Fitri Rahma Fridayana
AU - Seongju Lee
AU - Guo Nan Yin
AU - Ji-Kan Ryu
PY - 2026
DA - 2026/10/20
JO - Scientific Reports
DO - 10.1038/s41598-026-76434-8
UR - https://www.nature.com/articles/s41598-026-76434-8
AB - Peripheral nerve injury (PNI) disrupts neurovascular integrity and leads to persistent sensory and motor dysfunction. Insulin-like growth factor binding protein 5 (IGFBP5) regulates insulin-like growth factor bioavailability and has also been implicated in apoptosis, fibrosis, and extracellular matrix remodeling; however, its role in peripheral nerve regeneration remains unclear. This study investigated the temporal expression pattern of IGFBP5 following sciatic nerve injury (SNI) and examined whether its suppression is associated with early neurovascular regenerative responses. A murine SNI model was established, and IGFBP5 was silenced using perineural delivery of lentiviral short hairpin RNA. Neurovascular remodeling, cellular responses, and stress-related changes were evaluated at 5 days post-injury, and functional recovery was assessed longitudinally up to 12 weeks. We observed that IGFBP5 expression was markedly increased in both proximal and distal nerve segments after injury. IGFBP5 knockdown was associated with increased endothelial and axonal marker signals, accompanied by enhanced Schwann cell– and macrophage-associated responses and reduced myelin-associated signals. In parallel, reduced oxidative and nitrosative stress and decreased apoptotic markers were detected, together with increased proliferative activity during the early phase of regeneration. In addition, IGFBP5 suppression was associated with increased phosphorylation of PI3K–AKT and ERK signaling pathways. Functional assessments indicated improved motor recovery and higher sciatic functional index scores compared with controls. Together, these findings suggest that IGFBP5 knockdown is associated with a more favorable early neurovascular microenvironment following peripheral nerve injury. Targeting IGFBP5 may represent a potential strategy to modulate early regenerative processes, although further studies are required to define its mechanistic role and long-term effects.
SN - 2045-2322
ER -