Osteogenic potential of human umbilical cord-derived mesenchymal stromal cells cultured with umbilical cord blood-derived fibrin: A preliminary study

• Published in: Journal of cranio-maxillo-facial surgery 2013-12, Vol.41 (8), p.775-782
• Main Authors: Baba, Kyoko, Yamazaki, Yasuharu, Ishiguro, Masashi, Kumazawa, Kenichi, Aoyagi, Kazuya, Ikemoto, Shigehiro, Takeda, Akira, Uchinuma, Eiju
• Format: Article
• Language: English
• Subjects: Alkaline Phosphatase - analysis; Animals; Autologous tissue; Calcification, Physiologic - physiology; Cell Culture Techniques; Cell Differentiation - physiology; Core Binding Factor Alpha 1 Subunit - analysis; Culture Media; Dentistry; Fetal Blood - cytology; Fibrin; Fibrin - physiology; Humans; Male; Mesenchymal stromal cell; Mesenchymal Stromal Cells - physiology; Mice; Mice, Inbred BALB C; Mice, Nude; Microscopy, Electron, Scanning; Osteoblasts - physiology; Osteocalcin - analysis; Osteogenesis; Osteogenesis - physiology; Platelet-Rich Plasma - physiology; Regenerative medicine; Spectrometry, X-Ray Emission; Subcutaneous Tissue - surgery; Surgery; Tissue Scaffolds; Umbilical Cord - cytology; Umbilical cord blood; Wharton Jelly - cytology; X-Ray Microtomography
• ISSN: 1010-5182; 1878-4119
• DOI: 10.1016/j.jcms.2013.01.025

Abstract This study examined the potential for osteogenesis via regenerative medicine using autologous tissues (umbilical cord (UC) and umbilical cord blood (UCB)) in nude mice. The study was designed to provide the three elements required for regenerative medicine (cell, scaffold, and growth factor) and autoserum for culture by means of autologous tissues. Mesenchymal stromal cells were obtained from UC (UC-MSCs). Fibrin, platelet-rich-plasma, and autoserum were obtained from UCB as scaffold, growth factor and serum for culture respectively. UC-MSCs were obtained from Wharton jelly and cultured with UCB-derived fibrin (UCB-fibrin) for 3–4 weeks to induce their differentiation into osteoblasts. They were implanted subcutaneously into the dorsum of male nude mice for 6 weeks prior to undergoing assessment. The assessments performed were haematoxylin and eosin, and alizarin red staining, immunohistochemical staining of human mitochondria, scanning electron microscopy, scanning electron microscopy with energy dispersive X-ray spectrometry and real-time reverse transcriptase-polymerase chain reaction to assess the expressions of osteoblast markers. Consequently, the differentiation of UC-MSCs into osteoblasts and the production of hydroxyapatite were verified. This study suggested the possible formation of bone tissue using biomedical materials obtained from UC and UCB.