Insulin-like growth factor binding protein 4 loaded electrospun membrane ameliorating tendon injury by promoting retention of IGF-1

J Control Release. 2023 Apr:356:162-174. doi: 10.1016/j.jconrel.2023.02.039. Epub 2023 Mar 3.

Abstract

Tendon injury is one of the most common musculoskeletal disorders that impair joint mobility and lower quality of life. The limited regenerative capacity of tendon remains a clinical challenge. Local delivery of bioactive protein is a viable therapeutic approach for tendon healing. Insulin-like growth factor binding protein 4 (IGFBP-4) is a secreted protein capable of binding and stabilizing insulin-like growth factor 1 (IGF-1). Here, we applied an aqueous-aqueous freezing-induced phase separation technology to obtain the IGFBP4-encapsulated dextran particles. Then, we added the particles into poly (L-lactic acid) (PLLA) solution to fabricate IGFBP4-PLLA electrospun membrane for efficient IGFBP-4 delivery. The scaffold showed excellent cytocompatibility and a sustained release of IGFBP-4 for nearly 30 days. In cellular experiments, IGFBP-4 promoted tendon-related and proliferative markers expression. In a rat Achilles tendon injury model, immunohistochemistry and quantitative real-time polymerase chain reaction confirmed better outcomes by using the IGFBP4-PLLA electrospun membrane at the molecular level. Furthermore, the scaffold effectively promoted tendon healing in functional performance, ultrastructure and biomechanical properties. We found addition of IGFBP-4 promoted IGF-1 retention in tendon postoperatively and then facilitated protein synthesis via IGF-1/AKT signaling pathway. Overall, our IGFBP4-PLLA electrospun membrane provides a promising therapeutic strategy for tendon injury.

Keywords: Dextran particle; Electrospun membrane; IGF-1; IGFBP-4; Tendon injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Insulin-Like Growth Factor Binding Protein 4* / metabolism
  • Insulin-Like Growth Factor I
  • Quality of Life
  • RNA, Messenger / metabolism
  • Rats
  • Tendon Injuries* / drug therapy

Substances

  • Insulin-Like Growth Factor Binding Protein 4
  • Insulin-Like Growth Factor I
  • RNA, Messenger