Impact of injectable chitosan cryogel microspherescaffolds on differentiation and proliferation of adiposederived mesenchymal stem cells into fat cells

• DOI: 10.1177/08853282211048284
• Publication Date: 2021-12-30T09:34:46Z
• Authors: Duran Çekiç; Şakir Necat Yılmaz; Nimet Bölgen; Selma Ünal; Meltem Nass Duce; Gülsen Bayrak; Didem Demir; Merve Türkegün; Alper Sarı; Yavuz Demir; Şakir Ünal
• Keywords: Chitosan; 0303 health sciences; 03 medical and health sciences; Tissue Engineering; Tissue Scaffolds; Adipocytes; Animals; Cell Differentiation; Mesenchymal Stem Cells; Rabbits; Cryogels; Cell Proliferation

Difficulty in the clinical practice of stem cell therapy is often experienced in achieving desired target tissue cell differentiation and migration of stem cells to other tissue compartments where they are destroyed or die. This study was performed to evaluate if mesenchymal stem cells (MSCs) may differentiate into desired cell types when injected after combined with an injectable cryogel scaffold and to investigate if this scaffold may help in preventing cells from passing into different tissue compartments. MSCs were obtained from fat tissue of the rabbits as autografts and nuclei and cytoplasms of these cells were labeled with BrdU and PKH26. In Group 1, only-scaffold; in Group 2, only-MSCs; and in Group 3, combined stem cell/scaffold were injected to the right malar area of the rabbits. At postoperative 3 weeks, volumes of the injected areas were calculated by computer-tomography scans and histopathological evaluation was performed. The increase in the volume of the right malar areas was more in Group 3. In histopathological evaluation, chitosan cryogel microspheres were observed microscopically within the tissue and the scaffold was only partially degraded. Normal tissue form was seen in Group 2. Cells differentiated morphologically into fat cells were detected in Groups 2 and 3. Injectable chitosan cryogel microspheres were used in vivo for the first time in this study. As it was demonstrated to be useful in carrying MSCs to the reconstructed area, help cell differentiation to desired cells and prevent migration to other tissue compartments, it may be used for reconstructive purposes in the future.