CRYOPRESERVATION OF HIGHLY PURIFIED HUMAN PERIPHERAL BLOOD MONOCYTES.
[In Japanese. / En japonais.]
Author(s) : TAKAHASHI T. A.
Type of article: Article
Summary
HUMAN PERIPHERAL BLOOD MONOCYTES WERE PURIFIED BY COUNTERFLOW CENTRIFUGAL ELUTRIATION OF BUFFY COATS OBTAINED FROM NORMAL VOLUNTEERS. THE PURITY OF MONOCYTES WAS ABOUT 95% AND CELLULAR VIABILITY WAS HIGHER THAN 98%. THOSE HIGHLY PURIFIED MONOCYTES WERE SUSPENDED IN A MEDIUM CONTAINING 7.5% DMSO AND 5% FETAL CALF SERUM (OR 2% HUMAN SERUM ALBUMIN), AND FROZEN IN A PROGRAMMING FREEZER AT 1.25 K/MIN TO 193 K (-80 DEG C), PLUNGED INTO LIQUID NITROGEN (LN2 ) AND STORED FOR VARIOUS PERIOD (7-180 DAYS). THE NUMERICAL RECOVERY OF CRYOPRESERVED MONOCYTES STORED FOR 180 DAYS IN LN2 WAS 89%. FURTHERMORE, CRYOPRESERVED MONOCYTES (7 DAYS IN LN2 ) COULD PRODUCE INTERLEUKIN-L AFTER THE STIMULATION WITH LIPOPOLYSACCHARIDE FOR 24 HOURS, AND THOSE CELLS BECAME CYTOTOXIC AGAINST TUMORIGENIC CELLS.
Details
- Original title: [In Japanese. / En japonais.]
- Record ID : 1989-2521
- Languages: Japanese
- Source: Low Temperature Medicine - vol. 14 - n. 4
- Publication date: 1988
- Document available for consultation in the library of the IIR headquarters only.
Links
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Indexing
- Themes: The influence of refrigeration on cells, tissues and organs
- Keywords: Cryoprotectant; DMSO; Survival; Blood; Monocyte; Cryopreservation
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