An Elastin-Like Protein for Injectable Tissue-Like Network.
Yao Y., Kong Y., Long Y., Zhang X., Du L., Yang K.
Animal Study on Facial Rejuvenation, published in Biomacromolecules (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Animal Study
- Journal
- Biomacromolecules (2025)
- Country
- United States
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 40679103
- DOI
- 10.1021/acs.biomac.5c00536
Abstract (original English)
Protein-based tissue fillers are promising for adipose regeneration due to their biocompatibility and tunable properties. Inspired by elastin's structure, we designed a low-immunogenicity "multiple-domain-collective elastin-like" (MDCE) protein for injectable tissue-like networks. The MDCE protein was composed of thermal-responsive elastin-like peptides (disordered domains), polyalanine enrichment (functional ordered domains), and zwitterionic polypeptides (hydrophilic domains). This design endows the MDCE protein hydrogel with in situ injectability and antifouling properties, resulting in a tissue-like modulus-tunable filler formation in vivo without chemical cross-linkers and prevention of foreign body rejection. Adipose stem cells, encapsulated in the MDCE hydrogel, can maintain activity for at least ∼9 days (>80% survival rate). In a rat model of adipose tissue defect, a 3-month injection of MDCE hydrogel for efficiently filling adipose tissue presents superior stability and lower immunogenicity compared to the bovine-source elastin proteins. This work provides methods for tissue fillers and scaffolds, aiding medical regeneration, particularly facial rejuvenation.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
How we grade evidenceBrowse all related research
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