CuFi-5细胞
年限： 32 years
生长状态： 贴壁生长
ATCC Number： CRL-4016™
相关**： 囊肿性纤维化
运输方式： 冻存运输
器官来源： 肺
细胞类型： 其他细胞类型
细胞形态： 上皮样
是否是肿瘤细胞： 0
物种来源： 人
数量： 大量
组织来源： bronchus
Designations: CuFi-5
Depositors: AJ Klingelhutz
CuFi-5细胞Biosafety Level: 2
Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: adherent
Organism: Homo sapiens
Morphology: epithelial-like
Source: Organ: lung
Tissue: bronchus
Disease: cystic fibrosis
Cell Type: epithelial immortalized with hTERT and HPV-16 E6/E7-LXSN
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Isolation: Isolation date: 2001
Applications: CuFi-5细胞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.
Human airway epithelial (HAE) cell line, CuFi-5, was derived from lung of a 32-year-old patient with cystic fibrosis by retroviral infection with hTERT and HPV-16E6/E7. Consequently, the cells do not undergo growth arrest in cell culture due to exogenous expression of the telomerase and E6/E7 genes.
Other hTERT-immortalized cell lines derived from cystic fibrosis HAE are also available from ATCC as ATCC CRL-4013 (CuFi-1), ATCC CRL-4015 (CuFi-4), and ATCC CRL-4017 (CuFi-6).
Antigen Expression: positive for epithelial marker pan-cytokeratin (immunocytochemistry)
DNA Profile (STR): Amelogenin: X,Y
CSF1PO: 10,14
D13S317: 11,13
D16S539: 11,13
D5S818: 11,12
D7S820:11,12
THO1: 7
TPOX: 8,10
vWA: 16,17
Cytogenetic Analysis: This is a near-diploid cell line of male origin in which the most consistent karyotypic aberrations are trisomy of chromosomes 5 and 20. Other non-clonal aberrations were found at early passage, but the karyology tended to stabilize within several passages.
Age: 32 years
Gender: male
Comments: CuFi-5细胞Human airway epithelial (HAE) cell line, CuFi-5, was derived from lung of a 32-year-old patient with cystic fibrosis by retroviral infection with hTERT and HPV-16E6/E7. Consequently, the cells do not undergo growth arrest in cell culture due to exogenous expression of the telomerase and E6/E7 genes. [22566]
CuFi-5 cells are homozygous for the delta F508 cystic fibrosis-causing mutation (delta F508/delta F508).
Other hTERT-immortalized cell lines derived from cystic fibrosis HAE are also available from ATCC as ATCC CRL-4013 (CuFi-1), ATCC CRL-4015 (CuFi-4), and ATCC CRL-4017 (CuFi-6).
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. 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: These cells are grown in a serum-free medium: BEGM (Bronchial Epithelial Growth Medium, Serum-free) from Lonza (BEGM Bullet Kit; CC-3170) made of BEBM basal medium and SingleQuot additives (ATCC does not use gentamycin-amphotericin B) supplemented with 50 �g/ml G-418.
Temperature: 37.0°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Subculturing: Protocol:
Note: CuFi-5细胞The culture flasks should be pre-coated with 60µg/ml solution of Human Placental Collagen Type IV. (Sigma, Cat. No. C-7521) at least 18 hours in advance then air-dried and rinsed 2-3 times with Dulbecco's Phosphate Buffered Saline.
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 Trypsin-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°C to facilitate dispersal.
To remove Trypsin-EDTA solution, add 2.0 to 3.0 ml of 1% FBS in Dulbecco's Phosphate buffered Saline 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 1 x 104 to 2 x 104 viable cells/cm2 is recommended.
Incubate cultures at 37°C.
Subculture when cell concentration is between 3 x 104 and 4 x 104 cells/cm2.
Subcultivation ratio: A subcultivation ratio of 1:2 to 1:3 is recommended.
Medium renewal: every 2 to 3 days
Preservation: Freeze medium: BEGM with 30% FBS and 10% DMSO
Storage temperature: liquid nitrogen vapor phase
Doubling Time: approximately 36 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: CuFi-5细胞ATCC 4-X
Phosphate-buffered saline: ATCC 30-2200
References: 22566: Halbert CL, et al. The E7 gene of human papillomavirus type 16 is sufficient for immortalization of human epithelial cells. J. Virol. 65: 473-478, 1991. PubMed: 1845902
47354: Bodnar AG, et al. Extension of life-span by introduction of telomerase into normal human cells. Science 279: 349-352, 1998. PubMed: 9454332
92666: Zabner J, et al. Development of cystic fibrosis and noncystic fibrosis airway cell lines . Am. J. Physiol. Lung Cell Mol Physiol. 284: L844-L854, 2003. PubMed: 12676769
92667: Kiyono T, et al. Both Rb/p161NK4a inactivation and telomerase activity are required to immortalize human epithelial cells. Nature 396: 84-88, 1998. PubMed: 9817205
