The Inhibition of Lymphocyte Blastogenesis By L-Asparaginase

Author:

OHNO R.12,HERSH E. M.13

Affiliation:

1. Department of Developmental Therapeutics, The University of Texas M. D. Anderson Hospital and Tumor Institute at Houston, Houston, Texas.

2. The University of Texas M. D. Anderson Hospital and Tumor Research Institute at Houston, Houston, Texas. Present Address: First Department of Internal Medicine, Nagoya University School of Medicine, 65 Tsurunsaicho, Showa-Ku, Nagoya, Japan.

3. The University of Texas M. D. Anderson Hospital and Tumor Research Institute at Houston, Houston, Texas.

Abstract

Abstract The effect of the enzyme L-asparaginase on in vitro lymphocyte blastogenesis was studied. E.coli L-asparaginase has a reversible inhibitory effect on phytohemagglutinin (PHA) or specific antigen-induced lymphocyte blastogenesis. Five and one international units (I.U.) L-asparaginase per milliliter of culture media, suppressed lymphocyte blastogenesis almost completely. 0.5 I.U./ml. L-asparaginase showed a significant suppression and 0.1 I.U./ml. showed mild suppression. The effect was not due to direct toxicity of the enzyme, asparagine breakdown products, nor impure products of the enzyme preparation. The lymphocytes freed of L-asparaginase by washing after culture with the enzyme for up to 72 hours had normal responsiveness to PHA. The inhibitory effects of 0.1 I.U./ml. and 0.5 I.U./ml. of L-asparaginase were completely or partially counteracted by simultaneous administration of 2µmole/ml. L-asparagine, respectively. L-glutamine also counteracted the effect of L-asparaginase partially, but to a lesser degree than L-asparagine. Cell-density studies showed that 1 I.U./ml. of L-asparaginase, sufficient to inhibit the lymphocyte blastogenesis almost completely at the cell density of 0.5 x 106 and 1 x 106 lymphocytes, had less effect at higher cell population of 2.5 x 106 and 5 x 106. Lymphocytes once stimulated by PHA were partially resistant to L-asparaginase added during a later phase of the incubation period. The possible mechanism of this inhibition of L-asparaginase on lymphocyte blastogenesis was discussed. It is suggested that depletion of L-asparagine (both exogenous and endogenous) from the culture media would be the probable cause of this inhibitory effect.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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