Regeneration in Mice of Injured Skin, Heart, and Spinal Cord by α-Gal Nanoparticles Recapitulates Regeneration in Amphibians

• Published in: Nanomaterials (Basel, Switzerland) Vol. 14; no. 8; p. 730
• Main Authors: Galili, Uri, Li, Jianming, Schaer, Gary L
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.04.2024; MDPI
• Subjects: Amphibians; Amputation; Analysis; Angiogenesis; anti-Gal; Antibodies; Antigens; Axon sprouting; Axons; Biodegradation; Cholesterol; Complement; Complement activation; Complement system; Epitopes; Fetuses; Fibrosis; Genes; Heart; Heart attacks; Hypotheses; Identification and classification; Injuries; Macrophages; Methods; Monkeys & apes; Myocardial infarction; myocardial regeneration; Myocardium; Nanoparticles; Neonates; Properties; Regeneration; Regeneration (Biology); Reptiles & amphibians; Review; scar-free regeneration; Skin; skin regeneration; Spinal cord; Spinal cord injuries; spinal cord regeneration; Wound healing; α-gal nanoparticles; United States; complement activation; α-gal nanoparticles; scar-free regeneration; anti-Gal; spinal cord regeneration; myocardial regeneration; skin regeneration
• ISSN: 2079-4991; 2079-4991
• DOI: 10.3390/nano14080730

The healing of skin wounds, myocardial, and spinal cord injuries in salamander, newt, and axolotl amphibians, and in mouse neonates, results in scar-free regeneration, whereas injuries in adult mice heal by fibrosis and scar formation. Although both types of healing are mediated by macrophages, regeneration in these amphibians and in mouse neonates also involves innate activation of the complement system. These differences suggest that localized complement activation in adult mouse injuries might induce regeneration instead of the default fibrosis and scar formation. Localized complement activation is feasible by antigen/antibody interaction between biodegradable nanoparticles presenting α-gal epitopes (α-gal nanoparticles) and the natural anti-Gal antibody which is abundant in humans. Administration of α-gal nanoparticles into injuries of anti-Gal-producing adult mice results in localized complement activation which induces rapid and extensive macrophage recruitment. These macrophages bind anti-Gal-coated α-gal nanoparticles and polarize into M2 pro-regenerative macrophages that orchestrate accelerated scar-free regeneration of skin wounds and regeneration of myocardium injured by myocardial infarction (MI). Furthermore, injection of α-gal nanoparticles into spinal cord injuries of anti-Gal-producing adult mice induces recruitment of M2 macrophages, that mediate extensive angiogenesis and axonal sprouting, which reconnects between proximal and distal severed axons. Thus, α-gal nanoparticle treatment in adult mice mimics physiologic regeneration in amphibians. These studies further suggest that α-gal nanoparticles may be of significance in the treatment of human injuries.