PMID- 22697426 OWN - NLM STAT- MEDLINE DCOM- 20130416 LR - 20211021 IS - 1937-335X (Electronic) IS - 1937-3341 (Print) IS - 1937-3341 (Linking) VI - 18 IP - 21-22 DP - 2012 Nov TI - Fast-degradable microbeads encapsulating human umbilical cord stem cells in alginate for muscle tissue engineering. PG - 2303-14 LID - 10.1089/ten.TEA.2011.0658 [doi] AB - Human umbilical cord mesenchymal stem cells (hUCMSCs) are inexhaustible and can be obtained without an invasive surgery. To date, there has been no report on seeding hUCMSCs in three-dimensional scaffolds for muscle tissue engineering. The objectives of this study were to (1) investigate hUCMSC seeding in a scaffold for muscle engineering and (2) develop a novel construct consisting of hUCMSC-encapsulating and fast-degradable microbeads inside a hydrogel matrix. The rationale was that the hydrogel matrix would maintain the defect volume, while the microbeads would degrade to release the cells and concomitantly create macropores in the matrix. hUCMSCs were encapsulated in alginate-fibrin microbeads, which were packed in an Arg-Gly-Asp (RGD)-modified alginate matrix (AM). This construct is referred to as hUCMSC-microbead-AM. The control consisted of the usual cell encapsulation in AM without microbeads (referred to as hUCMSC-AM). In the hUCMSC-AM construct, the hUCMSCs showed as round dots with no spreading at 1-14 days. In contrast, cells in the hUCMSC-microbead-AM construct had a healthy spreading and elongated morphology. The microbeads successfully degraded and released the cells at 8 days. Myogenic expressions for hUCMSC-microbead-AM were more than threefold those of hUCMSC-AM (p<0.05). Immunofluorescence for myogenic markers was much stronger for hUCMSC-microbead-AM than hUCMSC-AM. Muscle creatine kinase of hUCMSC-microbead-AM at 14 days was twofold that of hUCMSC-AM (p<0.05). In conclusion, hUCMSC encapsulation in novel fast-degradable microbeads inside a hydrogel matrix was investigated for muscle engineering. Compared to the usual method of seeding cells in a hydrogel matrix, hUCMSC-microbead-AM construct had greatly improved cell viability and myogenic differentiation, and hence, is promising to enhance muscle regeneration. FAU - Liu, Jun AU - Liu J AD - Biomaterials and Tissue Engineering Division, Department of Endodontics, Prosthodontics and Operative Dentistry, University of Maryland Dental School, Baltimore, Maryland 21201, USA. FAU - Zhou, Hongzhi AU - Zhou H FAU - Weir, Michael D AU - Weir MD FAU - Xu, Hockin H K AU - Xu HH FAU - Chen, Qianming AU - Chen Q FAU - Trotman, Carroll Ann AU - Trotman CA LA - eng GR - R21 DE022625/DE/NIDCR NIH HHS/United States GR - R01 DE14190/DE/NIDCR NIH HHS/United States GR - R01 DE013814/DE/NIDCR NIH HHS/United States GR - R41 DE01974/DE/NIDCR NIH HHS/United States GR - R01 DE014190/DE/NIDCR NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20120719 PL - United States TA - Tissue Eng Part A JT - Tissue engineering. Part A JID - 101466659 RN - 0 (Alginates) RN - 0 (Hexuronic Acids) RN - 0 (Oligopeptides) RN - 25852-47-5 (Hydrogel, Polyethylene Glycol Dimethacrylate) RN - 78VO7F77PN (arginyl-glycyl-aspartic acid) RN - 8A5D83Q4RW (Glucuronic Acid) SB - IM MH - Alginates/*pharmacology MH - Biodegradation, Environmental MH - Cell Survival/drug effects MH - Cells, Immobilized/cytology/drug effects/metabolism MH - Gene Expression Regulation/drug effects MH - Glucuronic Acid/pharmacology MH - Hexuronic Acids/pharmacology MH - Humans MH - Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry MH - Mesenchymal Stem Cells/cytology/drug effects/metabolism MH - Microscopy, Electron, Scanning MH - *Microspheres MH - Muscle Development/drug effects/genetics MH - Muscles/drug effects/*physiology MH - Oligopeptides/pharmacology MH - Staining and Labeling MH - Stem Cells/*cytology/drug effects/metabolism MH - Tissue Engineering/*methods MH - Umbilical Cord/*cytology PMC - PMC3482877 EDAT- 2012/06/16 06:00 MHDA- 2013/04/17 06:00 PMCR- 2013/11/01 CRDT- 2012/06/16 06:00 PHST- 2012/06/16 06:00 [entrez] PHST- 2012/06/16 06:00 [pubmed] PHST- 2013/04/17 06:00 [medline] PHST- 2013/11/01 00:00 [pmc-release] AID - 10.1089/ten.tea.2011.0658 [pii] AID - 10.1089/ten.TEA.2011.0658 [doi] PST - ppublish SO - Tissue Eng Part A. 2012 Nov;18(21-22):2303-14. doi: 10.1089/ten.TEA.2011.0658. Epub 2012 Jul 19.