The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


The Journal of Immunology, 1973, 110: 1630-1637.
Copyright © 1973 by The American Association of Immunologists, Inc.

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 Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Coyne, J. A.
Right arrow Articles by David, J. R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Coyne, J. A.
Right arrow Articles by David, J. R.

Guinea Pig Lymphotoxin (LT)

II. Physicochemical Properties of LT Produced by Lymphocytes Stimulated with Antigen or Concanavalin A: Its Differentiation from Migration-Inhibitory Factor (MIF)1

John A. Coyne2, Heinz G. Remold3, Steven A. Rosenberg4 and John R. David

From the Departments of Medicine, Harvard Medical School and the Robert B. Brigham Hospital, Boston, Massachusetts 02120

Abstract

Guinea pig lymphotoxin (LT) produced by stimulation of sensitized lymph node cells, specifically by antigen or non-specifically by concanavalin A, was studied by methods previously used to characterize guinea pig migration-inhibitory factor. The results showed that LT induced by either antigen or mitogen was heat labile, eluted from Sephadex columns with peak activity in fractions containing molecules of 35,000 to 55,000 m.w., had an electrophoretic mobility at pH 9.1 similar to albumin and a buoyant density on CsCl similar to protein. It was destroyed by chymotrypsin but not by neuraminidase. These studies show that guinea pig LT can be readily differentiated from guinea pig migration-inhibitory factor. On the other hand, the LT produced by antigen stimulation has many features in common with LT produced by stimulation with concanavalin A.

Footnotes

1 This work was supported in part by United States Public Health Service Grant AI07685, National Institutes of Health Contract 71-2172, and a grant from the John A. Hartford Foundation.

2 Supported by United States Public Health Service Immunology Training Grant AI0036603.

3 Recipient of Cancer Research Scholar Award from the American Cancer Society.

4 Supported by United States Public Health Service Training Grant, Department of Surgery, Peter B. Brigham Hospital.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1973 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1973 by The American Association of Immunologists, Inc. All rights reserved.