1. 圣淘沙名胜世界(新加坡)

      CD34+ isolation from human bone marrow

      Mohsen Khosravi-Maharlooei, Markus Holzl, Austin Chen, Megan Sykes

      Published: 2021-09-24 DOI: 10.17504/protocols.io.bvswn6fe
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      Abstract

      This protocol details the steps for isolating CD34+ cells from human bone marrow. The CD34+ cells isolated from this protocol can be used for generating humanized mice through reconstitution of immune cells via IV injection after bone marrow ablation. These cells can also be used for mixed lymphocyte reaction experiments.

      Note
      Corresponding Authors Mohsen Khosravi-Maharlooei Email: mkm2182@cumc.columbia.eduAustin Chen Email: ac4274@cumc.columbia.eduTel: 425-283-6900

      Before start

      Human bone marrow is a rich source for CD34+ hematopoietic stem cells. CD34+ cells can be easily isolated and further processed.

      Steps

      1.

      Transfer the content of the collection bag into a sterile flask

      2.

      Add 250mLBM Medium to the bag and rinse it thoroughly

      3.

      Transfer the content of the collection bag into the sterile flask

      4.

      Layer 35mLof the suspension over 15mL of Histopaque

      5.

      Centrifuge the tubes for 30 minutes 500g without brake at RT

      6.

      Collect the leukocyte ring in 50mL Falcons and fill up with BM medium

      7.

      Wash once by centrifuging 6 minutes 500g

      8.

      Resuspend the cells in MACS buffer and count ( take for FACS confirmation = PRE 50µLfor FACS confirmation = PRE)

      9.

      Wash down again and resuspend the pellet according to the protocol (130-046-702 MACS Human CD34+ kit)

      10.

      Add 300µL of MACS buffer per 10^8 cells

      11.

      Add 100µL of FcR-B reagent per 10^8 cells, mix it and incubate in fridge for 15 minutes

      12.

      Add 100µLof CD34 beads per 10^8 cells to the suspension and mix and let it sit for 30 min (fridge)

      13.

      Fill up with 50mL MACS buffer and strain through a blue strainer (40 uM)

      14.

      Wash cells (500g6 min) and resuspend in MACS buffer 500 uL/200,000,000 cells. If you have more cells, increase volume accordingly. E.g 3 *10^9 cells = 7,5mL. Aliquot this volume to more than one (with 3mL prerinsed) MACS column.

      15.

      Wash with buffer 3mL 3 times and keep negative fraction ( Take 50µL for FCM = POST neg )

      16.

      Put the column out of the magnet and push out positive fraction with 5mL Buffer and the plunger

      17.

      Collect the positive fractions. (Take 50µL for FCM = Post pos)

      18.

      Process the cells as desired (injection in mouse or cryopreservation)

      19.

      Check the puritiy with FACS

      20.

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