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ATCC Number：CRL-2927?
數(shù)量：大量
年限：fetus, 8 weeks gestation
是否是腫瘤細(xì)胞：0
物種來(lái)源：人
組織來(lái)源：mesencephalon
運(yùn)輸方式：凍存運(yùn)輸
生長(zhǎng)狀態(tài)：貼壁生長(zhǎng)
細(xì)胞形態(tài)：神經(jīng)元
規(guī)格：0.5mg Designations: LUHMES
Depositors: ?J Lotharius
Biosafety Level:2
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
Organism: Homo sapiens
Morphology:neuronal


Source: Tissue: mesencephalon
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.
Isolation: Isolation date: 1998
DNA Profile (STR):Amelogenin: X
CSF1PO: 13,14
D5S818: 11,13
D13S317: 9,11
D7S820: 11,13
D16S539: 11,12
vWA: 14,17
THO1: 7,9.3
TPOX: 8
Age: fetus, 8 weeks gestation
Comments:The Lund human mesencephalic (LUHMES) cell line is a subclone of the tetracycline-controlled, v-myc-overexpressing human mesencephalic-derived cell line MESC2.10. MESC2.10 was originally immortalized with a LINX v-myc retroviral vector. [16173252 ] [16173253 ]
LUHMES cells can be differentiated into morphologically and biochemically mature dopamine-like neurons following exposure to tetracycline, GDNF (glial cell line-derived neurotrophic factor), and db-cAMP. LUHMES cells exhibit the same dopaminergic and neuronal characteristics as MESC2.10 cells. [16173253 ]
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:

• 1% N2 supplement (Gibco-Invitrogen Cat No 17502-048)
• 40 ng/ml b-FGF ( basic recombinant human Fibroblast Growth Factor; Gibco-Invitrogen Cat No 13256-029) added fresh at the last moment

Temperature: 37.0°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Subculturing: Flask Coating Procedure:
Culture flasks should be sequentially pre-coated with 50μg/ml poly-L-ornithine (Sigma, Cat. No. P-3655 or equivalent) and then with 1μg/ml Human Fibronectin (Sigma, Cat. No. F-0895 or equivalent).
Note: Use flasks with vented caps for best results.

1. Add 7.0 ml freshly diluted 50μg/ml poly-L-ornithine to T-75 sq cm flask and allow flask to sit over night at room temperature.
2. Remove and discard poly-L-ornithine solution. Rinse flask 3 times with sterile double distilled water. Discard last rinse and allow flask to air-dry uncapped and standing upright in a biological cabinet.
3. Add 5.0 ml freshly diluted 1μg/ml fibronectin and incubate 3 hours at 37°C.
4. Remove and discard fibronectin solution. Rinse flask 3 times with sterile water. Discard last rinse and allow flask to air-dry uncapped and standing upright in a biological cabinet.
5. Flask is ready for use when dry.

Protocol:
Subculture before cells reach 80% confluency.
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.
Note: Warm aliquots of wash medium (growth medium without bFGF) used in Step 4, freshly made complete growth medium and freshly diluted tryspin solution to 37°C prior to use.

1. Remove and discard culture medium.
2. Briefly rinse the cell layer with 10.0 ml Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS).
3. Add 4.0 ml of freshly diluted, pre-warmed 0.025% Trypsin-0.1 g/l EDTA solution (see formula below) to flask and incubate for 3 minutes at 37°C. Knock the flask several times against the palm of your hand to dislodge cells. Observe flask under an inverted microscope to be sure cells have come off.
4. Add 6.0 ml of pre-warmed wash medium (see Note above) and aspirate cells by gently pipetting.
5. Transfer cell suspension to a centrifuge tube and spin at approximately 190 xg for 7 minutes. Discard supernatant and knock the tube against the palm of your hand to loosen the cell pellet. Using a 1 ml pipet, add 1.0 ml complete growth medium and pipet the pellet up and down to resuspend the cells (avoid creating foam or bubbles).
6. Add an additional 2.0 ml of complete growth medium and dissociate cells further by pipetting up and down.
7. Adjust cell concentration by adding the necessary volume of complete growth medium needed to seed new flasks. Pipet up and down to evenly resuspend cells.
8. Add appropriate aliquots of the cell suspension to new pre-coated vented culture flasks.
9. Incubate cultures in 5% CO₂ /95% air at 37°C.

2X Trypsin-EDTA Solution:
2X Trypsin-EDTA solution is 0.05% Trypsin-0.2g/l EDTA. Before use, this must be diluted 1:1 in Ca++/Mg++ free Dulbucco?s phosphate-buffered saline (D-PBS) to 0.025% Trypsin ? 0.1g/l EDTA

To make 1 liter of 2X Trypsin-EDTA solution:

1. Add the following to 500 ml ddH₂ O:
   • 8 g NaCl
   • 0.4 g KCL
   • 0.58 g NaHCO₃
   • 1 g Dextrose
   • 0.2 g EDTA
   • 0.5 g Trypsin (Sigma, Cat. No. T7409)
2. Bring volume up to 1 liter with ddH₂ O, and pH to 7.4 with HCL.
3. Incubate at 37°C for at least 1 hour to activate the trypsin.
4. Sterile filter (0.2 μm) and make aliquots.
5. Refrigerate at 4°C overnight and then store at -20°C.
6. Before use, dilute trypsin 1:1 with Ca++/Mg++ free Dulbucco?s phosphate-buffered saline (D-PBS) and warm to 37°C.

Subcultivation ratio: A subcultivation ratio of 1:3 to 1:4 is recommended. Subculture approximately every 3 to 4 days.
Medium renewal: Every 2 to 3 days
Preservation: Freeze medium: complete growth medium supplemented with 20% fetal bovine serum and 10% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Related Products:Recommended medium (without the additional serum described under ATCC Medium): ATCC 30-2006
Cell culture tested DMSO: ATCC 4-X
Recommended serum: ATCC 30-2020
Phosphate-buffered saline: ATCC 30-2200
References: 16173252: Lotharius J, et al. Progressive degeneration of human mesencephalic neuron-derived cells triggered by dopamine-dependent oxidative stress is dependent on the mixed-lineage kinase pathway. J. Neurosci. 25 (27) : 6329-6342, 2005. PubMed: 16000623
16173253: Lotharius J, et al. Effect of mutant alpha-synuclein on dopamine homeostasis in a new human mesencephalic cell line. J. Bio.Chem. 277(41): 38884-388894, 2002. PubMed: 12145295