Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (28)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Freed, K. A.
Right arrow Articles by Rice, G. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Freed, K. A.
Right arrow Articles by Rice, G. E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Human Reproduction, Vol 3, 493-499, Copyright © 1997 by Oxford University Press


JOURNAL ARTICLE

Differential expression of type II, IV and cytosolic PLA2 messenger RNA in human intrauterine tissues at term

KA Freed, EK Moses, SP Brennecke and GE Rice
Department of Perinatal Medicine, Royal Women's Hospital, Carlton, Victoria, Australia.

The involvement of phospholipase A2 (PLA2) enzymes in the formation of biologically-active phospholipid metabolites by human gestational tissues has principally been characterized by the use of enzyme activity assays. While such assays have established the presence of functional PLA2 activity, there is a paucity of information concerning the tissue distribution and relative contribution to net activity made by specific PLA2 isozymes. In particular, both secretory and cytosolic isozymes may be involved in gestational tissue phospholipid metabolism. Thus, the aim of this study was to test the hypothesis that phospholipase A2 mRNA transcripts encoding Type II, Type IV and cytosolic PLA2 are tissue-specifically expressed in human amnion, choriodecidua and placenta obtained at term. The relative expression of polyA+ mRNA encoding these PLA2 isozymes was determined by Northern blot analysis and laser densitometry. The data obtained confirm the tissue-specific expression of PLA2 mRNA in human intrauterine tissues. Cytosolic PLA2 mRNA was most abundantly expressed in amnion when compared to either choriodecidua (which was 5-fold less than amnion; P < 0.001) or placenta (72-fold less than amnion; P < 0.001). In contrast, the secretory PLA2 mRNA transcripts (i.e. Type II and Type IV) were most abundantly expressed in placenta. Type II PLA2 mRNA expression in choriodecidua and amnion was 30-fold less than that observed in placenta (both P < 0.001). Type IV PLA2 mRNA expression was 37-fold (P < 0.001) and 73-fold (P < 0.001) less in choriodecidua and amnion respectively. These data support the conclusion that cytosolic PLA2 is the principal PLA2 isozyme mediating phospholipid metabolism and the liberation of fatty acid substrate (i.e. arachidonic acid) in term amnion, while secretory PLA2 isozymes, and in particular, Type II PLA2 play a major role in phospholipid metabolism in term placenta.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
EndocrinologyHome page
L. Gao, C. Lu, C. Xu, Y. Tao, B. Cong, and X. Ni
Differential Regulation of Prostaglandin Production Mediated by Corticotropin-Releasing Hormone Receptor Type 1 and Type 2 in Cultured Human Placental Trophoblasts
Endocrinology, June 1, 2008; 149(6): 2866 - 2876.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
M. G. Farina, S. Billi, G. Leguizamon, C. Weissmann, T. Guadagnoli, M. L. Ribeiro, and A. M. Franchi
Secretory and cytosolic phospholipase A2 activities and expression are regulated by oxytocin and estradiol during labor
Reproduction, August 1, 2007; 134(2): 355 - 364.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
K. Brant, W. Guan, P. Tithof, and R. L. Caruso
Gestation Age-Related Increase in 50-kDa Rat Uterine Calcium-Independent Phospholipase A2 Expression Influences Uterine Sensitivity to Polychlorinated Biphenyl Stimulation
Biol Reprod, May 1, 2006; 74(5): 874 - 880.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
A. Varastehpour, T. Radaelli, J. Minium, H. Ortega, E. Herrera, P. Catalano, and S. Hauguel-de Mouzon
Activation of Phospholipase A2 Is Associated with Generation of Placental Lipid Signals and Fetal Obesity
J. Clin. Endocrinol. Metab., January 1, 2006; 91(1): 248 - 255.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
D. M. Slater, S. Astle, P. R. Bennett, and S. Thornton
Labour is associated with increased expression of type-IIA secretory phospholipase A2 but not type-IV cytosolic phospholipase A2 in human myometrium
Mol. Hum. Reprod., November 1, 2004; 10(11): 799 - 805.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
D. M. Slater, S. Zervou, and S. Thornton
Prostaglandins and Prostanoid Receptors in Human Pregnancy and Parturition
Reproductive Sciences, May 1, 2002; 9(3): 118 - 124.
[Abstract] [PDF]


Home page
Mol Hum ReprodHome page
B. Kleine, S. Wolfahrt, M. Lotsch, T. Gantner, and W. G. Rossmanith
Expression of galanin in human placenta
Mol. Hum. Reprod., April 1, 2001; 7(4): 379 - 385.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
M. D. Rosenthal, E. D. Albrecht, and G. J. Pepe
Developmental Maturation of Baboon Placental Trophoblast: Expression of Messenger Ribonucleic Acid and Protein Levels of Cytosolic and Secretory Phospholipases A2
J. Clin. Endocrinol. Metab., August 1, 1998; 83(8): 2861 - 2867.
[Abstract] [Full Text]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.