Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  Cancer Health Disparities Conference 2009
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 47, 47-50, January 1, 1987]
© 1987 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Okutomi, T.
Right arrow Articles by Yamazaki, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Okutomi, T.
Right arrow Articles by Yamazaki, M.

Induction of Release of Cytotoxin from Murine Bone Marrow Cells by an Animal Lectin

Takafumi Okutomi, Yuki Nakajima, Fusao Sakakibara, Hiroaki Kawauchi and Masatoshi Yamazaki1

Faculty of Pharmaceutical Sciences, Teikyo University, Sagamiko, Kanagawa 199-01 [T. O., Y. N., M. Y.], and Institute of Cancer Research, Tohoku College of Pharmaceutical Sciences, Sendai, Miyagi 983 [F. S., H. K.], Japan

An animal lectin purified from loach (Misgurnus anguillicaudatus) eggs induced release of cytotoxin from fresh bone marrow cells from mice, although the other lectins tested, wheat germ agglutinin, concanavalin A, and phytohemagglutinin did not. The cytotoxin released from bone marrow cells was a heat-labile protein with a molecular weight of 70,000. The main cells responsible for release of M, 70,000 cytotoxin seemed to be of macrophage lineage, since they adhered to plastic and were sensitive to certain antibodies for markers of macrophages. However, they did not express asialo GM1 antigen which is expressed by activated macrophages. Removal of cells that phagocytized iron did not diminish but rather enhanced the release of cytotoxin. Therefore, active bone marrow cells appeared to be immature, not mature macrophages. These data suggest that immature bone marrow cells that are not specifically activated have a cytolytic potency against tumor cells and that internal animal lectins may induce release of the cytotoxin from these cells.

1 To whom requests for reprints should be addressed.

Received 3/11/86. Revised 6/12/86. Revised 8/27/86. Accepted 9/10/86.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1987 by the American Association for Cancer Research.