| Literature DB >> 35032910 |
Priya Katyal1, Aubryanna Hettinghouse2, Michael Meleties1, Sadaf Hasan2, Changhong Chen2, Min Cui2, Guodong Sun2, Rajiv Menon3, Bonnie Lin1, Ravinder Regatte3, Jin Kim Montclare4, Chuan-Ju Liu5.
Abstract
Protein-based biomaterials offer several advantages over synthetic materials, owing to their unique stimuli-responsive properties, biocompatibility and modular nature. Here, we demonstrate that E5C, a recombinant protein block polymer, consisting of five repeats of elastin like polypeptide (E) and a coiled-coil domain of cartilage oligomeric matrix protein (C), is capable of forming a porous networked gel at physiological temperature, making it an excellent candidate for injectable biomaterials. Combination of E5C with Atsttrin, a chondroprotective engineered derivative of anti-inflammatory growth factor progranulin, provides a unique biochemical and biomechanical environment to protect against post-traumatic osteoarthritis (PTOA) onset and progression. E5C gel was demonstrated to provide prolonged release of Atsttrin and inhibit chondrocyte catabolism while facilitating anabolic signaling in vitro. We also provide in vivo evidence that prophylactic and therapeutic application of Atsttrin-loaded E5C gels protected against PTOA onset and progression in a rabbit anterior cruciate ligament transection model. Collectively, we have developed a unique protein-based gel capable of minimally invasive, sustained delivery of prospective therapeutics, particularly the progranulin-derivative Atsttrin, for therapeutic application in OA.Entities:
Keywords: Atsttrin; Injectable protein engineered gels; Post traumatic osteoarthritis; Progranulin; Rabbit anterior cruciate ligament transection model; Recombinant block polymer gels; Sustained delivery
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Year: 2022 PMID: 35032910 PMCID: PMC9055922 DOI: 10.1016/j.biomaterials.2022.121370
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 15.304