人单核细胞和中性粒细胞

Purpose

Materials

• 10ml 6% dextran + 7ml citrate/citric acid

• Dextran: T500 --> 6g+100ml PBS

• Citrate solution: 25g Na Citrate + 8g citric acid + 500 ml PBS

• 43 ml blood

• 12 ml RT Histopaque 1077

• 18 ml cold H₂ O

• 2 ml 10x PBS

• M199 for HUVECs: 1L powder pocket M199 + 35g NaHCO₃ + 25mM Hepes + 5 mM glutamine + 50 ug/ml Gentamycin.

• 1M Hepes: 119.1 g Hepes + 500 ml dH₂ O.

• Media A: 1X HBSS (10X:50ml) + 10 mM Hepes (1M: 5 ml) + 5 mM EDTA (0.5M: 5ml) + 2.5 % FBS (12.5 ml) in 500 ml.

• Media B: RPMI1640 470 ml + Gent (1000X) 0.5 ml + Glutamine (100X) 5 ml + 5% FBS (25 ml)

Procedure

1. Draw venous blood into 60 ml syringe with 10ml 6% dextran + 7 ml citrate/citric acid. Fill to 60 ml total (blood 43 ml).

2. Mix and sediment 30 min at RT (white blood cells now with serum).

3. Transfer serum/white blood cells to 50 ml tube, underlay 12 ml RT Histopaque 1077.

4. Spin 2500 rpm/30min at RT.

To take mononuclear cells:

1. Take off serum above band. (See attached figure, in preparation)

2. Take mononuclear band + some Ficoll into two 15ml tubes.

3. Add cold media A up to 15ml.

4. Spin at 1800 rpm 4^o C for 5min.

5. Pool pellet into one 15ml tube and add cold media A.

6. Wash cells three times (1400 rpm, 4^o C, for 5 min) to remove platelets.

7. Add media B and count cells.

To take neutrophils:

1. Remove mononuclear band and serum with suction. (See attached figure, in preparation)

2. Wash in PBS (or media A) to remove Histopaque (spin 1800 rpm/5 min at 4^o C)

3. Remove PBS (or media A) , add 18 ml cold H₂ O to lyse RBC, and add 2 ml 10x PBS.

4. Spin 1400 rpm/5min at 4^o C.

5. Wash as needed, resuspend, and count cells.