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This study describes a method to construct aggregates based on the self-assembly of human mesenchymal stem cells and identifies the morphological and histological characteristics for the regenerative treatment of cranial bone defects.
Mesenchymal stem cells (MSCs), characterized by their self-renewal ability and multilineage differentiation potential, can be derived from various sources and are emerging as promising candidates for regenerative medicine, especially for regeneration of the tooth, bone, cartilage, and skin. The self-assembled approach of MSC aggregation, which notably constructs cell clusters mimicking the developing mesenchymal condensation, allows high-density stem cell delivery along with preserved cell-cell interactions and extracellular matrix (ECM) as the microenvironment niche. This method has been shown to enable efficient cell engraftment and survival, thus promoting the optimized application of exogenous MSCs in tissue engineering and safeguarding clinical organ regeneration. This paper provides a detailed protocol for the construction and characterization of self-assembled aggregates based on umbilical cord mesenchymal stem cells (UCMSCs), as well as an example of the cranial bone regenerative application. The implementation of this procedure will help guide the establishment of an efficient MSC transplantation strategy for tissue engineering and regenerative medicine.
Mesenchymal stem cell (MSC) condensation is an essential stage to ensure the normal growth and development of the body in early organogenesis1,2, especially in the formation of bone, cartilage, teeth, and skin1,3,4. In the last few decades, tissue engineering therapies using cultured postnatal MSCs combined with biodegradable scaffolds have made important advances in osteogenic5 and cartilaginous regeneration6. However, the use of scaffolds may have some disadvantages, s....
NOTE: All animal procedures were approved by the Animal Care and Use Committee of the Fourth Military Medical University and performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. Cryopreserved human UCMSCs that were obtained from a commercial source were used for the present study (see Table of Materials). The use of human cells was approved by the Ethics Committee of the Fourth Military Medical University. UCMSCs were taken as an example to desc.......
Aggregates can be successfully constructed from UCMSCs according to the experimental workflow (Figure 1). The quality of aggregates must be evaluated prior to use, via morphological observation and histological analysis. The lamellar structure formed should be complete and dense, with the cells interlaced to form a woven pattern by microscopic observation (Figure 2A). Edge curling can be discovered during aggregation; overcurling edges indicate unsucces.......
With the advances of tissue engineering biotechnology, strategies to construct an implantable structure with high plasticity and containing long-term-surviving cells that can achieve optimal regeneration have been the focus of many scientists. There are a variety of current implantation methods of MSCs, such as cell-only methods, scaffolds complemented with cytokines6,24, or the combination of stem cells and scaffolds5. This paper presents.......
This work was supported by grants from the National Natural Science Foundation of China (81930025, 82100969, and 82071075) and the National Key Research and Development Program of China (2022YFA1104400 and 2021YFA1100600). We are grateful for the assistance of the National Experimental Teaching Demonstration Center for Basic Medicine (AMFU).
....Name | Company | Catalog Number | Comments |
0.25% Trypsin-EDTA (1x) | Sigma | T4049 | Cell passage |
Automatic Dehydration Machine | LEICA | ASP200s | Dehydrate aggregate |
Centrifuge | Eppendorf | 5418R | Centrifugation |
Centrifuge tube | Thermo Nunc | 339650 | Centrifugation |
Culture dish | Thermo | 150466 | Culture of UCMSCs |
Ethanol | SCR | 10009218 | Dehydrate aggregate |
Fatal bovine serum | Sijiqing | 11011-8611 | Culture of UCMSCs |
Forcep | JZ | JD1080 | Harvest aggregate |
Glutaraldehyde | Proandy | 10217-1 | Fixation of aggregate |
Hematoxylin and Eosin Staining Kit | beyotime | C0105S | HE staining |
Hexamethyldisilazane | SCR | 80068416 | Dry aggregate surface |
Hoechst33342 | Sigma | 14533 | Cell nuclei stain |
L-glutamine | Sigma | G5792 | Culture of UCMSCs |
Live/dead Viability/Cytotoxicity Kit | Invitrogen | L3224 | Live/dead cell stain |
Masson's Staining Kit | ZHC | CD069 | Masson Staining |
Minimum Essential Medium Alpha basic (1x) | Gibco | C12571500BT | Culture of UCMSCs |
Paraffin | Leica | 39601006 | Tissue embedding |
Paraformaldehyde | Saint-Bio | D16013 | Fixation of aggregate |
PBS (1x) | Meilunbio | MA0015 | Resuspend and purify UCMSCs |
Penicillin/Streptomycin | Procell Life Science | PB180120 | Culture of UCMSCs |
Pentobarbital sodium | Sigma | P3761 | Animal anesthesia |
Polysporin | Pfizer | Prevent eye dry | |
Scanning Electron Microscope | Hitachi | s-4800 | SEM observation |
Scissor | JZ | Y00030 | Animal surgical incision |
Six-well plate | Thermo | 140675 | Culture of UCMSCs |
Stitch | Jinhuan | F603 | Close wounds |
Suture | Xy | 4-0 | Close wounds |
Thermostatic equipment | Grant | v-0001-0005 | Water bath |
UCMSCs | Bai'ao | UKK220201 | Commercially UCMSCs |
Vitamin C | Diyibio | DY40138-25g | Aggregate inducing |
Xylene | SCR | 10023418 | Dehydrate aggregate |
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