RN33B细胞
年限： 12.5 days gestation embryo
ATCC Number： CRL-2825™
细胞形态： 其他
细胞类型： 其他细胞类型
是否是肿瘤细胞： 0
物种来源： 褐鼠
生长状态： 贴壁生长
器官来源： 大脑
数量： 大量
品系： Sprague-Dawley
组织来源： medullary raphe nucleus
运输方式： 冻存运输
Designations: RN33B
Depositors: SR Whittemore
RN33B细胞Biosafety Level: 2 [cells containing SV40 viral DNA sequences ]
Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: adherent
Organism: Rattus norvegicus
Morphology: spindle-shaped at 33C; neurite-like at 37C
Source: Strain: Sprague-Dawley
Organ: brain
Tissue: medullary raphe nucleus
Cell Type: neuronalSV40 large T antigen transfected
Cellular Products: enolase
nestin
neurofilament
vimentin
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. RN33B细胞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.
Isolation: Isolation date: February, 1988
Receptors: nerve growth factor (NGF), expressed
Temperature Effects: Restrictive temperature: 37 to 39°C cells differentiate into neurons
Permissive temperature: 33°C cells proliferate
Y
Age: 12.5 days gestation embryo
Comments: RN33B is an neuronal cell line derived from medullary raphe cells by infection with a retrovirus encoding the temperature-sensitive mutant of SV40 large T antigen. The cells were cloned by serial dilution.At the permissive temperature of 33C, RN33B cells divide and express SV40 T antigen, vimentin, nestin, diffuse neuron-specific enolase, and low and medium molecular weight neurofilament immunoreactivities.At the non-permissive temperature of 37C to 39C SV40 T antigen expression is markedly decreased and RN33B cells cease mitotic activity and differentiate with phase bright cell bodies and 'neuritic-like' processes.RN33B细胞Differentiated RN33B cells express enhanced neuronal-specific protein expression but do not synthesize astrocytic or oligodendrocytic-specific proteins. Moreover, differentiated RN33B cells returned to 33C re-express T antigen, but do not de-differentiate or begin dividing. Immunohistochemical and Northern blot analysis revealed high levels of low affinity NGF receptor protein and mRNA in differentiated RN33B cells. PCR analysis demonstrated the presence of trkB, but not trkA or trkC, mRNA in both undifferentiated and differentiated RN33B cells. The cells can be used as a model of neuronal differentiation in vitro.
Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated DMEM:F12 Medium Catalog No. 30-2006. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 33.0°C
Subculturing: Protocol:
Remove and discard culture medium.
Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.
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 33C to facilitate dispersal.
Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
Add appropriate aliquots of the cell suspension to new culture vessels.
An inoculum of 5 X 10(3) to 8 X 10(3) viable cells/sq. cm is recommended.
RN33B细胞Incubate cultures at 33C.
Interval: Maintain cultures at a cell concentration between 3 X 10(4) and 1 X 10(5) cells/sq. cm
Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:6 is recommended
Medium Renewal: Two to three times weekly
Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Doubling Time: 20 hours
Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2006
recommended serum:ATCC 30-2020
References: 89616: Whittemore SR, White LA. Target regulation of neuronal differentiation in a temperature-sensitive cell line derived from medullary raphe. Brain Res. 615: 27-40, 1993. PubMed: 8364724
89617: Shihabuddin LS, et al. The ***** CNS retains the potential to direct region-specific differentiation of a transplanted neuronal precursor cell line. J. Neurosci. 15: 6666-6678, 1995. PubMed: 7472427
89618: Wojciechowski AB, et al. Long-term survival and glial differentiation of the brain-derived precursor cell line RN33B after subretinal transplantation to ***** normal rats. Stem Cells 20: 163-173, 2002. PubMed: 11897873
89619: Warfvinge K, et al. Retinal integration of grafts of brain-derived precursor cell lines implanted subretinally into *****, normal rats. Exp. Neurol. 169: 1-12, 2001. PubMed: 11312552
