Immortalized Human Cord Blood Mesenchymal Stromal Cells (cbMSC-hTERT)

Cat.No.: CSC-I9207L

Species: Homo sapiens

Source: Umbilical cord blood

Morphology: Fibroblast-like

Culture Properties: Adherent

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Cat.No.
CSC-I9207L
Description
Owing to its multiple differentiation abilities, the Mesenchymal stromal cells (MSCs) holds the promise in tissue engineering and regenerative medicine, and displays important clinical potential for cell therapy. The Immortalized Human Cord Blood Mesenchymal Stromal Cells (cbMSC-hTERT) retains MSC specific surface markers (CD29, CD73, CD105, CD44 and HLA-ABC) as well as its differentiation capacities into cells of the mesodermal lineage, such as osteoblasts and adipocytes. In addition, karyotype analysis and CGH analysis show no chromosomal abnormality nor genomic deletion or amplifications, making this cell line suitable for stem cell research and translational study.Similarly, the Immortalized Human Cord Blood Mesenchymal Stromal Cells with RFP (cbMSC-hTERT-RFP) exhibits comparable characteristics as cbMSC-hTERT with the addition of red fluorescent protein labelling. Transplantation of cbMSC-hTERT-RFP into the rat model with TBI demonstrates that these cells are readily attracted to the injury area and thus provides a valuable cell-based tool for stem cell transplantation andin vivodetection.
Species
Homo sapiens
Source
Umbilical cord blood
Culture Properties
Adherent
Morphology
Fibroblast-like
Immortalization Method
Serial passaging and transfection with Human Telomerase Reverse Transcriptase (hTERT) expression vector pGRN145
Markers
CD29, CD73, CD105, CD44 and HLA-ABC
Application
For Research Use Only
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until cell culture needed for experiments.

Note: Never can cells be kept at -20 °C.
Shipping
Dry Ice.
Recommended Products
CIK-HT003 HT® Lenti-SV40T Immortalization Kit
CIK-HT013 HT® Lenti-hTERT Immortalization Kit
Quality Control
1) RT-PCR was used to confirm the expression of the hTERT transgene in the immortalized cells;
2) TRAP assay was performed to determine the telomerase activity;
3) Flow cytometry was used to detect surface markers such as CD29, CD73, CD105, CD44 and HLA-ABC;
4) G-banding was used for karyotype analysis;
5) Tumuorigenicity assay was performed to evaluate the cells’ tumorigenic potential.
BioSafety Level
II
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Immortalized human cord‑blood mesenchymal stromal cells (cbMSC‑hTERT) are an extensively characterized, hTERT‑transduced MSC line with an origin in neonatal umbilical cord blood. Parental cells are extracted from the blood component of the umbilical cord, a fetal tissue that naturally harbors large quantities of primitive mesenchymal progenitors. Subsequent retroviral transduction with human telomerase reverse transcriptase (hTERT) confers the cells with unlimited proliferative capacity. The classic MSC phenotype is retained, including plastic adherence, fibroblast‑like morphology, and immunophenotype characterized by expression of CD29, CD44, CD73, CD90, CD105 and HLA‑ABC with lack of hematopoietic markers CD14, CD34 and CD45.

The line features a doubling time of ~24 h and can be passaged to >20 generations without evidence of senescence. Karyotype analysis and comparative genomic hybridization analysis have demonstrated stability of the genome. In vivo tumorigenicity assays in immunodeficient mice have not demonstrated evidence of malignant transformation and the line is considered a non‑tumorigenic, BSL‑2 research tool. Functionally, cbMSC‑hTERT demonstrates vigorous trilineage differentiation capacity to form mineralized matrix in osteogenic differentiation, lipid droplets in adipogenic differentiation, and proteoglycan rich matrix in chondrogenic differentiation culture conditions.

Due to its capacity for infinite expansion, stable phenotype, and non‑tumorigenic safety profile, cbMSC‑hTERT is a broadly useful tool for studies in basic MSC biology, tissue‑engineering scaffold seeding, high‑throughput drug screens, disease model construction, and in vivo cell tracking studies (e.g., RFP‑labelled derivatives in traumatic brain injury or multiple sclerosis models).

Cell Viability of Stromal Cell-Derived Factor-1 Contained in Gelatin/Hyaluronate Copolymer Mixed with Hydroxyapatite

Bone defects from orthopedic trauma are difficult to manage. Here, Chang's team fabricated a Gel/HA copolymer with HAP and SDF-1 to enhance bone regeneration. Cell viability and proliferation were assessed using WST-1 assays. Target cbMSC-hTERT cells were treated with different media extracts. In the positive control group, 0.2 g/mL zinc diethyldithiocarbamate was added; in the negative control group, 0.2 g/mL aluminum oxide was used. The composite group received 0.2 g/mL Gel/HA-HAP. Untreated controls were set at 100% viability. Figure 1 shows that cbMSC-hTERT cell growth was unaffected in the Gel/HA-HAP and negative control groups, while the positive control group showed significant viability reduction. ANOVA revealed significant differences only in the positive control group compared to the other three groups.

Viability of cells.

Fig. 1. Viability of cells (Chang Y-L, Hsieh C-Y, et al., 2021).

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