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Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)

It has been reported that β‐1,3‐d‐glucan isolated from Alcaligenes faecalis (TAK) promoted tumor cytolysis by mouse polymorphonuclear leukocytes (PMN). We investigated the effect of serum on mouse PMN tumor cytolysis induced by TAK and other PMN stimulators. Addition of fetal calf serum (FCS) to the...

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Detalles Bibliográficos
Autores principales: Araki, Akemi, Inoue, Tomio, Kimura, Seishi, Fukase, Shigeru, Sendo, Fujiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917947/
https://www.ncbi.nlm.nih.gov/pubmed/2108949
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02509.x
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author Araki, Akemi
Inoue, Tomio
Kimura, Seishi
Fukase, Shigeru
Sendo, Fujiro
author_facet Araki, Akemi
Inoue, Tomio
Kimura, Seishi
Fukase, Shigeru
Sendo, Fujiro
author_sort Araki, Akemi
collection PubMed
description It has been reported that β‐1,3‐d‐glucan isolated from Alcaligenes faecalis (TAK) promoted tumor cytolysis by mouse polymorphonuclear leukocytes (PMN). We investigated the effect of serum on mouse PMN tumor cytolysis induced by TAK and other PMN stimulators. Addition of fetal calf serum (FCS) to the cytolysis assay enhanced tumor cytolysis by PMN in a dose‐dependent manner. Sera obtained from horses, mice, and rats were also effective enhancers of PMN tumor cytolysis. When FCS was added after the assay was under way, the enhancing effect decreased proportionally to the time elapsed. The enhancing activity was detected over a broad range of fractions with a peak at 170 kD by fractionation on a Superose 6 column. The responsible factor(s) in serum was stable after treatment at 60°C, 30 min or after lowering the pH to 2. Mouse PMN stimulated with TAK increased production of hydrogen peroxide in the presence of FCS.
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spelling pubmed-59179472018-05-11 Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s) Araki, Akemi Inoue, Tomio Kimura, Seishi Fukase, Shigeru Sendo, Fujiro Jpn J Cancer Res Article It has been reported that β‐1,3‐d‐glucan isolated from Alcaligenes faecalis (TAK) promoted tumor cytolysis by mouse polymorphonuclear leukocytes (PMN). We investigated the effect of serum on mouse PMN tumor cytolysis induced by TAK and other PMN stimulators. Addition of fetal calf serum (FCS) to the cytolysis assay enhanced tumor cytolysis by PMN in a dose‐dependent manner. Sera obtained from horses, mice, and rats were also effective enhancers of PMN tumor cytolysis. When FCS was added after the assay was under way, the enhancing effect decreased proportionally to the time elapsed. The enhancing activity was detected over a broad range of fractions with a peak at 170 kD by fractionation on a Superose 6 column. The responsible factor(s) in serum was stable after treatment at 60°C, 30 min or after lowering the pH to 2. Mouse PMN stimulated with TAK increased production of hydrogen peroxide in the presence of FCS. Blackwell Publishing Ltd 1990-01 /pmc/articles/PMC5917947/ /pubmed/2108949 http://dx.doi.org/10.1111/j.1349-7006.1990.tb02509.x Text en
spellingShingle Article
Araki, Akemi
Inoue, Tomio
Kimura, Seishi
Fukase, Shigeru
Sendo, Fujiro
Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)
title Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)
title_full Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)
title_fullStr Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)
title_full_unstemmed Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)
title_short Enhancement of Polymorphonuclear Leukocyte‐mediated Tumor Cytotoxicity by Serum Factor(s)
title_sort enhancement of polymorphonuclear leukocyte‐mediated tumor cytotoxicity by serum factor(s)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917947/
https://www.ncbi.nlm.nih.gov/pubmed/2108949
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02509.x
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