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


     
 


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
Right arrow Citation Map
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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ikehara, S.
Right arrow Articles by Modak, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ikehara, S.
Right arrow Articles by Modak, M. J.

The Journal of Immunology, Vol 127, Issue 5 1834-1838, Copyright © 1981 by American Association of Immunologists


ARTICLES

Adenosine-5'-triphosphate-(ATP) mediated stimulation and suppression of DNA synthesis in lymphoid cells. I. Characterization of ATP responsive cells in mouse lymphoid organs

S Ikehara, RN Pahwa, DG Lunzer, RA Good and MJ Modak

The effects of various nucleotides and nucleosides on DNA synthesis of mouse lymphocyte populations were studied. Significant stimulation of DNA synthesis was observed in the cells from bone marrow or the thymus in the presence of ATP. In contrast, the DNA synthesis of the cells from spleen, lymph nodes, and peripheral blood was markedly inhibited by ATP. Guanosine 5'-triphosphate had nonspecific stimulatory effects on the DNA synthesis of various lymphoid cells, whereas cytidine triphosphate had no effect. When thymocytes or bone marrow cells were separated by 1 x g velocity sedimentation, a distinct cell population was identified as being responsible for the ATP-mediated stimulation of DNA synthesis. Further characterization of ATP-responsive cells revealed that the highest concentration of terminal deoxynucleotidyl transferase, a marker enzyme for precursor T cells, was present in these cells. ATP-mediated stimulation of DNA synthesis may, therefore, serve as a specific marker restricted to a certain population of differentiating T cells.


This article has been cited by other articles:


Home page
J. Immunol.Home page
X. Duhant, L. Schandene, C. Bruyns, N. S. Gonzalez, M. Goldman, J.-M. Boeynaems, and D. Communi
Extracellular Adenine Nucleotides Inhibit the Activation of Human CD4+ T Lymphocytes
J. Immunol., July 1, 2002; 169(1): 15 - 21.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
F. Di Virgilio, P. Chiozzi, D. Ferrari, S. Falzoni, J. M. Sanz, A. Morelli, M. Torboli, G. Bolognesi, and O. R. Baricordi
Nucleotide receptors: an emerging family of regulatory molecules in blood cells
Blood, February 1, 2001; 97(3): 587 - 600.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
O. R. Baricordi, L. Melchiorri, E. Adinolfi, S. Falzoni, P. Chiozzi, G. Buell, and F. Di Virgilio
Increased Proliferation Rate of Lymphoid Cells Transfected with the P2X7 ATP Receptor
J. Biol. Chem., November 19, 1999; 274(47): 33206 - 33208.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. J. Gilbert, T. R. Pettitt, S. D. Seatter, S. D. Reid, M. J. O. Wakelam, and M. M. Harnett
Antagonistic Roles for Phospholipase D Activities in B Cell Signaling: While the Antigen Receptors Transduce Mitogenic Signals Via a Novel Phospholipase D Activity, Phosphatidylcholine-Phospholipase D Mediates Antiproliferative Signals
J. Immunol., December 15, 1998; 161(12): 6575 - 6584.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
P. E. Ross, G. R. Ehring, and M. D. Cahalan
Dynamics of ATP-induced Calcium Signaling in Single Mouse Thymocytes
J. Cell Biol., September 8, 1997; 138(5): 987 - 998.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1981 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1981 by The American Association of Immunologists, Inc. All rights reserved.