NuLi-1細胞

生長狀態(tài)： 貼壁生長

ATCC Number： CRL-4011?

運輸方式： 凍存運輸

器官來源： 肺（及支氣管）

細胞形態(tài)： 上皮樣

年限： 36

數(shù)量： 大量

是否是腫瘤細胞： 0

物種來源： 人

Designations: NuLi-1

Depositors: AJ Klingelhutz

NuLi-1細胞Biosafety Level: 2 [cells containing SV40 and HPV viral DNA sequences ]

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens deposited as Homo sapiens

Morphology: epithelial

Source: Organ: lung; bronchus

Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.

Restrictions: This material requires that the Addendum for Commercial and For-Profit Organizations or the Addendum for Noncommercial and Academic Organizations be signed and returned to ATCC before shipment. The price listed above is for noncommercial and academic organizations only. Commercial and for-profit organizations should call for pricing.

Isolation: Isolation date: 2000

Applications: NuLi-1細胞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.

DNA Profile (STR): Amelogenin: X,Y

Cytogenetic Analysis: This is a near-diploid human cell line of male origin with a polyploidy rate of 24%. There were copies of karyotypically normal X and Y-chromosomes present in most of the cells analyzed. Overall, some of the cells contained chromosomal abnormalities, with the most consistent being trisomy 5 and 20.

Age: 36

Gender: male

Comments: Human airway epithelial (HAE) cell line, NuLi-1, was derived from normal lung of a 36-year-old patient by dual retroviral infection with HPV-16E6/E7-LXSN [Pubmed: 1845902] and hTERT-LXSN [Pubmed: 9817205]. Consequently, the cells do not undergo growth arrest in cell culture due to exogenous expression of the telomerase and E6/E7 genes. NuLi-1 cells (wild type) do not express the delta F508 cystic fibrosis-causing mutation. Another hTERT-immortalized cell line, derived from HAE of a cystic fibrosis patient is also available as ATCC CRL-4013 (CuFi-1). Both cell lines, when seeded on semipermeable filters and grown at the air-liquid interface, are capable of forming polarized differentiated epithelia that exhibit transepithelial resistance and maintain the ion channel physiology expected of each genotype. These cell lines may be useful models for studying ion physiology, therapeutic interventions for cystic fibrosis and innate immunity [Pubmed: 12676769].

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. We have also compared its karyotype, telomerase expression level, growth rate, morphology and tissue-specific markers when first recovered from cryopreservation with that of cells at 10+ population doublings to ensure that there is no change in these parameters and that the cells are capable of extended proliferation.

Propagation: NuLi-1細胞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.

Atmosphere: 5% CO2 in air recommended

Temperature: 37.0°C

Subculturing: Protocol:

Note: The culture flasks should be pre-coated with 60ug/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 sq.cm. 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 x g 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 9 X 10(3) to 1.5 X 10(4) viable cells/sq. cm is recommended.

Incubate cultures at 37C.

Subculture when cell concentration is between 4 X 10(4) and 5 X 10(4) cells/sq. cm.

Subcultivation Ratio: 1:5

Medium Renewal: Every 2-3 days (do not wait longer)

Preservation: Freeze medium: BEGM with 30% FBS and 10% DMSO

Storage temperature: liquid nitrogen vapor phase

Doubling Time: about 43 hours

Related Products: recommended serum:ATCC 30-2020

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. NuLi-1細胞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