June 2020
Volume 61, Issue 7
ARVO Annual Meeting Abstract  |   June 2020
Hyaluronan derived from the limbus is a key Regulator of Corneal Lymphangiogenesis
Author Affiliations & Notes
  • Mingxia Sun
    University of Houston, Houston, Texas, United States
  • Sudan Puri
    University of Houston, Houston, Texas, United States
  • Kazadi Nadine Mutoji
    University of Houston, Houston, Texas, United States
  • Yvette May Coulson-Thomas
    Universidade Federal de São Paulo, São Paulo, Brazil
  • Vincent Hascall
    Cleveland Clinic, Ohio, United States
  • David G Jackson
    University of Oxford, United Kingdom
  • Tarsis F Gesteira
    University of Houston, Houston, Texas, United States
  • Vivien Jane Coulson-Thomas
    University of Houston, Houston, Texas, United States
  • Footnotes
    Commercial Relationships   Mingxia Sun, None; Sudan Puri, None; Kazadi Mutoji, None; Yvette Coulson-Thomas, None; Vincent Hascall, None; David Jackson, None; Tarsis Gesteira, None; Vivien Coulson-Thomas, None
  • Footnotes
    Support  NIH grant EY029289
Investigative Ophthalmology & Visual Science June 2020, Vol.61, 3550. doi:
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      Mingxia Sun, Sudan Puri, Kazadi Nadine Mutoji, Yvette May Coulson-Thomas, Vincent Hascall, David G Jackson, Tarsis F Gesteira, Vivien Jane Coulson-Thomas; Hyaluronan derived from the limbus is a key Regulator of Corneal Lymphangiogenesis. Invest. Ophthalmol. Vis. Sci. 2020;61(7):3550.

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      © ARVO (1962-2015); The Authors (2016-present)

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Purpose :
Corneal lymphangiogenesis and angiogenesis leads to the loss of corneal transparency. We have recently shown that in the cornea hyaluronan (HA) is present primarily in the limbal region and plays a key role regulating the limbal stem cell phenotype. Given the HA receptor LYVE-1 is highly expressed in corneal lymphatic vessels we investigated whether HA could play a role in regulating corneal lymphangiogenesis.

Methods : Wild-type (wt) and hyaluronan synthase (HAS) knockout mice - specifically combined Has1-/- and Has3 -/- null mice (HAS1-/-;HAS3-/-) and conditional Has2 knock-out mice (HAS2D/DCorEpi), were used. The mice were subjected to injury, alkali burn or suture placement, to investigate the role of HA on corneal lymphangiogenesis. Corneal buttons were also obtained from different developmental time-points to study the role of HA in lymphatic vessel development. The corneas were analyzed by whole mount immunohistochemistry and entire corneas were imaged under an LSM 800 confocal microscope using the both the z-stack and tiling mode. Primary lymphatic vessel endothelial cells from human dermis (hDLECs) and lymph node (hLLECs) were used for tube formation assay and cell proliferation assay in vitro.

Results : After injury both wild-type and HAS1-/-;HAS3-/- mice presented both an increase in HA expression and lymphangiogenesis. Interestingly, lymphatic vessels extended exclusively into HA rich areas. In stark contrast, HAS2D/DCorEpi mice did not upregulate HA synthesis after injury and, in turn, did not present lymphangiogenesis. Our developmental studies revealed first HA is expressed in the corneal limbus and thereafter lymphatic vessels invade this region. Our in vitro studies corroborated our in vivo data, with both HA increasing the proliferation and tube formation ability of hDLECs and hLLECs.

Conclusions :
HA regulates corneal lymphangiogenesis, both during development and after injury. These findings raise the possibility that therapeutic blockade of HA-mediated lymphangiogenesis could be used to reduce corneal scarring and also prevent rejection after corneal transplantation.

This is a 2020 ARVO Annual Meeting abstract.


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