help button home button Am J Pathol International Conference on Pathology of Chest Diseases
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Order Full text via Infotrieve
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gerrard, J. M.
Right arrow Articles by White, J. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gerrard, J. M.
Right arrow Articles by White, J. G.

American Journal of Pathology, Vol 100, 609-618, Copyright © 1980 by American Society for Investigative Pathology


REGULAR ARTICLES

Lysophosphatidic acids: III. Enhancement of neutrophil chemotaxis

JM Gerrard, CC Clawson and JG White

1-Palmitoyl-lysophosphatidic acid (LPA) was studied for its influence on the chemotaxis and ultrastructure of human neutrophils. By itself, LPA had no effect on the indices of chemotaxis or random migration of neutrophils. However, LPA on either the cellular or attractant side of Boyden chambers significantly enhanced the chemotactic responses of neutrophils to suboptimal concentrations of formyl-methionyl- phenylalanine. The enhancement of chemotaxis was achieved with concentrations of LPA (120-240 microM) that had no effect alone on neutrophil ultrastructure. The results, taken together with recent advances in knowledge of the role of the phosphatidylinositol turnover response in mediating effects of stimulating agents on cells, may provide a novel concept for understanding neutrophil chemotaxis.


This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
M. Murph, T. Tanaka, S. Liu, and G. B. Mills
Of Spiders and Crabs: The Emergence of Lysophospholipids and Their Metabolic Pathways as Targets for Therapy in Cancer.
Clin. Cancer Res., November 15, 2006; 12(22): 6598 - 6602.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
D. L. Hunton, W. G. Barnes, J. Kim, X.-R. Ren, J. D. Violin, E. Reiter, G. Milligan, D. D. Patel, and R. J. Lefkowitz
{beta}-Arrestin 2-Dependent Angiotensin II Type 1A Receptor-Mediated Pathway of Chemotaxis
Mol. Pharmacol., April 1, 2005; 67(4): 1229 - 1236.
[Abstract] [Full Text] [PDF]


Home page
J BiochemHome page
K. Arai, S. Yoshida, M. Nakatani, S. Fujiwara, T. Yubisui, and K. Kawamura
Phospholipids and Their Derivatives as Mitogen and Motogen of Budding Tunicates
J. Biochem., January 1, 2004; 135(1): 71 - 78.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
K. A. Carnevale and M. K. Cathcart
Calcium-Independent Phospholipase A2 Is Required for Human Monocyte Chemotaxis to Monocyte Chemoattractant Protein 1
J. Immunol., September 15, 2001; 167(6): 3414 - 3421.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
L. G. Fischer, M. Bremer, E. J. Coleman, B. Conrad, B. Krumm, A. Gross, M. W. Hollmann, G. Mandell, and M. E. Durieux
Local Anesthetics Attenuate Lysophosphatidic Acid-Induced Priming in Human Neutrophils
Anesth. Analg., April 1, 2001; 92(4): 1041 - 1047.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1980 by the American Society for Investigative Pathology.