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Effects of Fibroin Microcarriers on Inflammation and Regeneration of Deep Skin Wounds in Mice

A. Y. Arkhipova1#, M. A. Nosenko1,2#, N. V. Malyuchenko1, R. V. Zvartsev2, A. M. Moisenovich2, A. S. Zhdanova1,2, T. V. Vasil’eva1, E. A. Gorshkova1,2, I. I. Agapov3, M. S. Drutskaya1,2*, S. A. Nedospasov1,2,4, and M. M. Moisenovich1

1Lomonosov Moscow State University, Biological Faculty, 119991 Moscow, Russia; E-mail: marinadru@gmail.com

2Engelhardt Institute of Molecular Biology, 119991 Moscow, Russia

3Shumakov Research Institute of Transplantation and Artificial Organs, Russian Ministry of Health, 113182 Moscow, Russia

4Lomonosov Moscow State University, Belozersky Institute of Physico-Chemical Biology, 119991 Moscow, Russia

# These authors contributed equally to this work.

* To whom correspondence should be addressed.

Received June 21, 2016; Revision received July 20, 2016
The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative potential of biological material is related to its ability to modulate the inflammatory response. At the same time, all foreign materials, once implanted into a living tissue, to varying degree cause an immune reaction. The modern approach to the development of bioengineered structures for applications in regenerative medicine should be directed toward using the properties of the inflammatory response that improve healing, but do not lead to negative chronic manifestations. In this work, we studied the effect of microcarriers comprised of either fibroin or fibroin supplemented with gelatin on the dynamics of the healing, as well as inflammation, during regeneration of deep skin wounds in mice. We found that subcutaneous administration of microcarriers to the wound area resulted in uniform contraction of the wounds in mice in our experimental model, and microcarrier particles induced the infiltration of immune cells. This was associated with increased expression of proinflammatory cytokines TNF, IL-6, IL-1β, and chemokines CXCL1 and CXCL2, which contributed to full functional recovery of the injured area and the absence of fibrosis as compared to the control group.
KEY WORDS: proinflammatory cytokines, microparticles, fibroin, IL-6, TNF

DOI: 10.1134/S0006297916110031