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Last updated date: Jul 2, 2021 Views: 819 Forks: 0
Cell isolation from 3 Mice (SECs, KCs & HSCs)
Pronase E (Roche 10-165-921-001)
Collagenase D (Roche 11-088-874-103)
DNase I (Roche 10-104-159-001)
1) Preparation of 6 kinds of solution
A) SC-1 solution 200ml
B) SC-2 solution 150ml + pronase E 50mg
C) SC-2 solution 150ml + collagenase D 100mg
D) SC-2 100ml + pronase E 50mg+collagenase D 50mg + DNase 1ml (DNase I solution: Adjust 2mg/ml using GBSS/B. Store at -20ºC)
E) Nycodenz 1 (AXIS-SHIELD): 5.18g/total volime 15ml by GBSS/A Filtered through 0.2um.
F) Nycodenz 2 (AXIS-SHIELD): 3.63g/total volume 25ml by GBSS/A Filtered through 0.2um.
2) Filter those solutions (0.2m Bottle top filter)
3) Incubate A), B) and C) in the water bath (40ºC)
4) Insert 27G catheter into Portal vein and fasten by a vascular crump and cut IVC.
5) Perfuse (5ml/min) A) SC-1 solutionfor 5min.
6) Perfuse (5ml/min) B) pronase E/SC-2 solution for 5 min.
7) Perfuse (5ml/min) C) collagenase D/SC-2 solution for 5min.
8) Take the liver out. Keep on ice in 50ml SC-2 solution.
9) Tear membrane gently
10) Transfer the tissue into beaker. Add D) solution (collagenase 50mg + pronase 50mg + DNase 1ml/ total volume 150ml by SC-2 solution).
11) Incubate at 37ºC for 20 minutes with gently stirring.
12) Filter the digested liver though a cell strainer (70μm nylon).
13) Transfer to 3 Falcon tube (50ml). Centrifuge 500 rpm for 1min at 4ºC.
14) Transfer supernatant to 3 Falcon tube (50ml). Discard or keep the pellet (Hepatocyte).Centrifuge 2000 rpm for 8 min at 4ºC.
15) Resuspend each pellet in 10ml of GBSS/B containing 150μl of DNase I.
16) Collect each cell suspension into 2 Falcon tube (50ml).
17) Add GBSS/B up to 50ml. Centrifuge 2000 rpm (500g) for 8 min at 4ºC.
18) Discard supernatant.
19) Add 10ml of GBSS/B containing 150μl of DNase I andresuspend pellet.
20) Collect each cell suspension into 1 Falcon tube (50ml).
21) Add GBSS/B up to 34ml and add 14ml of E) Nycodenz 1 solution. Mix well. Total volume:50ml
22) Prepare 14.5% F) Nycodenz 2 solution (3.63g Nycodenz /GBSS-A 25ml). Transfer 4ml into 6 tubes (FALCON 15ml tube).
23) Lay 8.3ml of 21) onto the 14.5% Nycodenz solution.
24) Lay 1ml of GBSS/B onto the solution.
25) Centrifuge 3000rpm for 20min at 4ºC. Do not use Break!
26) Under the first layer of clear GBSS/B solution, you can see white layer. This layer contains stellate cell. Collect this layer and transfer to new 50ml tube. The second layer contains SEC & KC. Collect this layer and transfer to new 50ml tube.
27) Add GBSS/B solution to wash and centrifuge 1500rpm for 7min at 4ºC .
28) HSC; Count cells. Culture in DMEM+10% FBS on a plastic dish.
29) KC; Plate for 20min on a plastic dish and wash 3times by PBS. Culture in RPMI1640 +10%FBS.
SEC; Supernatant contains SEC. If you need the high purity, you should do MACS procedure for SEC. SEC should be culture on the collagen coated plate in special medium.)
CC-3156 EBM-2 Basal Medium 500ml
CC-4176 EBM-2 Single Quot Kit Suppl. & Growth Factors.
(Clonetics, LONZA)
SC-1 SC-2
NaCl 8000mg/L 8000mg/L
KCl 400mg/L 400mg/L
NaH2PO4. H2O 88.17mg/L 88.17mg/L
Na2HPO4 120.45mg/L 120.45mg/L
HEPES 2380mg/L 2380mg/L
NaHCO3 350mg/L 350mg/L
EGTA 190mg/L (-)
Glucose 900mg/L (-)
CaCl2. 2H2O (-) 560mg/L
pH: 7.20~7.30 by 1N NaOH
GBSS (Gey’s balanced salt solution)
GBSS-A GBSS-B
NaCl (-) 8000mg/L
KCl 370mg/L 370mg/L
MgCl2. 6H2O 210mg/L 210mg/L
MgSO4. 7H2O 70mg/L 70mg/L
Na2HPO4. 59.6mg/L 59.6mg/L
KH2PO4 30mg/L 30mg/L
Glucose 991mg/L 991mg/L
NaHCO3 227mg/L 227mg/L
CaCl2. 2H2O 225mg/L 225mg/L
pH: 7.20~7.30
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