CP-C (CP-94251)细胞
生长状态： 贴壁生长
数量： 大量
组织来源： epithelium
运输方式： 冻存运输
年限： *****
ATCC Number： CRL-4029™
相关**： Barrett食管
细胞类型： 其他细胞类型
器官来源： 食道
细胞形态： 上皮样
是否是肿瘤细胞： 0
CP-C (CP-94251)细胞物种来源： 人
Designations: CP-C (CP-94251)
Depositors: B. Reid
Biosafety Level: 2
Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: adherent
Organism: Homo sapiens
Morphology: epithelial-like
Source: Organ: esophagus
Tissue: epithelium
Cell Type: high-grade dysplasia
Disease: Barrett's esophagus
Immortalization method: hTERT expression
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Isolation: Isolation date: September 1995
Applications: In addition, it has been verified that no gross changes are observed in karyotype and morphology during the first 10 population doublings.
As part of our quality control, we have tested this cell line for its ability to grow for a minimum of 15 population doublings after recovery from cryopreservation.
The Barrett's esophagus cell line, CP-C (also identified as CP-94251) was derived from an endoscopic biopsy specimen obtained from a region of high-grade dysplasia.
Genetic instability studies using flow cytometry and FISH reveal the retention of elevated tetraploidy (G2/tetraploidy) in the hTERT-immortalized cells similar to the non-transduced parental cells.
Morphologically, the cell line is similar to early passage cultures exhibiting smaller cells with large nucleus to cytoplasm ratio.
Antigen Expression: positive for epithelial marker pan-cytokeratin (immunocytochemistry)(verified at ATCC )
negative for gastric mucin (CLH2) (immunocytochemistry)(verified at ATCC )
DNA Profile (STR): CP-C (CP-94251)细胞CSF1PO: 9, 13
D13S317: 8, 10
D16S539: 11, 12
D5S818: 12
D7S820: 8, 11
THO1: 8, 9.3
TPOX: 8
vWA: 17
Amelogenin: XY
Age: *****
Gender: male
Comments: The Barrett's esophagus cell line, CP-C (also identified as CP-94251) was derived from an endoscopic biopsy specimen obtained from a region of high-grade dysplasia. The cells were immortalized by transduction with a retroviral expression vector, pLXSN-hTERT, to create an immortalized cell line. [16173160]
Terminal restriction fragment lengths (TRF) analyses show the cells have increased telomerase activity and extended telomeres of about 12 kb. Morphologically, the cell line is similar to early passage cultures exhibiting smaller cells with large nucleus to cytoplasm ratio. Genetic instability studies using flow cytometry and FISH reveal the retention of elevated tetraploidy (G2/tetraploidy) in the hTERT-immortalized cells similar to the non-transduced parental cells. [16173161]
This well-characterized pre-malignant culture represents a unique tool for studying esophageal cancer progression.
As part of our quality control, we have tested this cell line for its ability to grow for a minimum of 15 population doublings after recovery from cryopreservation. CP-C (CP-94251)细胞In addition, it has been verified that no gross changes are observed in karyotype and morphology during the first 10 population doublings.
Propagation: ATCC complete growth medium: The base medium for this cell line is MCDB-153. To make the complete growth medium, add the following components to the base medium:
0.4 �g/ml hydrocortisone
20 ng/ml recombinant human EGF (Epidermal Growth Factor)
1 nM cholera toxin
20 mg/L adenine
140 �g/ml BPE (Bovine Pituitary Extract)
0.1% ITS [Insulin-Transferrin-Sodium Selenite Supplement(Sigma, I1884)]
4 mM glutamine
fetal bovine serum to a final concentration of 5%
Temperature: 37.0°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Subculturing: Protocol: Volumes used in this protocol are for 75 cm2 flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
Remove and discard culture medium.
Add 2.0 to 3.0 ml of 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37.0°C to facilitate dispersal.
Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
Transfer cell suspension to a centrifuge tube and spin at approximately 125 xg for 5 to 10 minutes. Discard supernatant.
Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to new culture vessels. An inoculum of 2 X 104 to 3 X 104 viable cells/cm2 is recommended.
Incubate cultures at 37.0°C. Subculture when cells reach a concentration between 7 X 104 and 1 X 105 cells/cm2.
Subcultivation ratio: A subcultivation ratio of 1:2 to 1:4 is recommended.
Medium renewal: every 3 to 4 days
Preservation: Freeze medium: RPMI-1640 Medium, 80%; fetal bovine serum, 10%; DMSO, 10%
Storage temperature: liquid nitrogen vapor phase
Doubling Time: approximately 58 hours
Related Products: Recommended serum: ATCC 30-2020
0.25% (w/v) Trypsin - 0.53mM EDTA in Hank's BSS (w/o Ca++, Mg ++): ATCC 30-2101
Cell culture tested DMSO: ATCC 4-X
Recommended base medium for freezing (without the additional serum described under Freeze Medium): ATCC 30-2001
References: 16173160: Palanca-Wessels MC, et al. Genetic Analysis of Long-term Barrett's Esophagus Epithelial Cultures Exhibiting Cytogenetic and Ploidy Abnormalities. Gastroentrology 114:114-295, 1998. PubMed: 9453489
16173161: Palanca-Wessels MC, et al. Extended lifespan of Barrett's esophagus epithelium transduced with the human telomerase catalytic subunit: a useful in vitro model. Carcinogenesis 24(7): 1183-1190, 2003. PubMed: 12807723
16173615: Barrett MT, et al. Molecular Phenotype of Spontaneously Arising 4N (G2-Tetraploid) Intermediates of Neoplastic Progression in Barrett's Esophagus. Cancer Res. 63: 4211-4217, 2003. PubMed: 12874028
16173616: Maley CC, et al. Genetic clonal diversity predicts progression to esophageal adenocarcinoma. Nat. Genet. 38(4): 468-473, 2006. PubMed: 16565718
