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Lysophospholipids and lysophospholipase D in rabbit aqueous humor following corneal injury

  • Akira Tokumura(corresponding author)
    ,
  • Satoshi Taira
    ,
  • Masaki Kikuchi
    ,
  • Toshihiko Tsutsumi
    ,
  • Yoshibumi Shimizu
    ,
*Corresponding author for this work
  • Tokushima University
    ,
  • Kyushu University of Health and Welfare
    ,
  • University of Tennessee Health Science Center
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

We previously found that lysophosphatidic acid (LPA)-like activity eliciting Cl - currents in Xenopus oocytes is increased in rabbit aqueous humor (AH) following corneal freeze wounds. The purpose of this study was to examine whether actual levels of LPA in AH from wounded eyes are higher than those from control eyes, and to determine the sources and enzymatic pathways of AH LPA in control and wounded conditions. Lysophospholipase D (lysoPLD) activity was measured by the enzymatic determination of choline following incubation of AH samples with exogenous lysophosphatidylcholines (LPCs). The molecular species compositions of LPA and LPC in fresh and incubated AH were determined by liquid chromatography-tandem mass spectrometry. A high, but similar activity of lysoPLD in the samples from both control and freeze-wounded eyes was detected. Its enzymatic properties resemble those of plasma lysoPLD, identified as autotaxin. Levels of LPCs, predominant substrates of lysoPLD in AH, were several times higher in the AH samples from injured eyes than those from the control eyes. Our results suggest that lysoPLD is constitutively released from corneal tissues and/or ciliary body into the AH, with no injury-induced increase in release following freeze-wounding. They also suggest that wound-induced increases in LPA-like biological activity are due to linoleoyl species-rich molecular composition in AH from wounded eyes. A possible mechanism of the altered molecular composition is an increase in the AH concentrations of LPCs, linoleoyl species of which are preferentially converted to corresponding unsaturated LPA by the constitutively active lysoPLD.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 83-89 (7 pages)

Journal (Volume, Issue Number)

Prostaglandins and Other Lipid Mediators (Volume 97, Issue 3-4)

Publication milestones

  • Published - 03/2012

Publication status

Published - 03/2012

ISSN

1098-8823

Publication IDs

  • Scopus: 84858701049
  • PubMed: 22281604

Publication metrics

Metrics

Scopus
citations
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1
SciVal
FWCI
0.55
SciVal
Author count
6
SciVal
citations
7
SciVal
Paper percentile
59

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Captures
16
Citation count
8

Funding Details

The authors wish to thank Dr. Junken Aoki, Tohoku University for his kind providing rat monoclonal anti-ATX antibody and Dr. Miguel Coca-Prados for kindly providing us with ciliary body epithelial cells. The authors also thank technical assistance of Aya Fukuda and Wako Hatuyama, University of Tokushima. This work was supported by a Grant-in-Aid for Scientific Research from Ministry of Education, Science, Sports and Culture of Japan (AT), and a grant from the National Scleroderma Foundation (MAW) .