July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
The PEXpress lncRNA/hnRNPL complex regulates signaling and morphology of human Schlemm’s canal cells
Author Affiliations & Notes
  • Heather Schmitt
    Ophthalmology, Duke University, Durham, North Carolina, United States
  • William Johnson
    Ophthalmology, Duke University, Durham, North Carolina, United States
  • Shelby Strickland
    Ophthalmology, Duke University, Durham, North Carolina, United States
  • Michael A Hauser
    Ophthalmology, Duke University, Durham, North Carolina, United States
  • William D Stamer
    Ophthalmology, Duke University, Durham, North Carolina, United States
  • Footnotes
    Commercial Relationships   Heather Schmitt, None; William Johnson, None; Shelby Strickland, None; Michael Hauser, None; William D Stamer, None
  • Footnotes
    Support  Grant from LC Industries
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 3185. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Heather Schmitt, William Johnson, Shelby Strickland, Michael A Hauser, William D Stamer; The PEXpress lncRNA/hnRNPL complex regulates signaling and morphology of human Schlemm’s canal cells. Invest. Ophthalmol. Vis. Sci. 2019;60(9):3185.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : Pseudoexfoliation glaucoma (PEXG) is the most common secondary form of open angle glaucoma worldwide. PEXpress is a lncRNA located within the LOXL1 locus, which is associated with high risk of PEXG. We have previously shown that (i) the risk variants alter PEXpress promoter strength, (ii) mechanical stretch of Schlemm’s canal (SC) cells increases PEXpress expression, (iii) PEXpress specifically complexes with hnRNPL, a RNA regulation protein and (iv) knockdown of PEXpress changes expression levels of 300+ genes in B3 cells. The goal of the present study was to examine the role of PEXpress in modulating hnRNPL splicing activity and mechanotransduction signaling.

Methods : Adenoviruses encoding shRNA targeted to PEXpress or hnRNPL were used to alter their expression in SC cells. At 4 days post-transduction, cell lysates were collected for Western blot analyses. Mechanotransduction and adhesion hub proteins FAK, AKT, and MAPK were monitored for state of activation. We also examined hnRNPL splicing activity on glaucoma relevant substrates, eNOS and CD44 V10. Morphological changes were determined in monolayers of SC cells by immunofluorescence.

Results : Knockdown of PEXpress in SC cells significantly increased the proportion of phosphorylated AKT to total AKT (p=0.008), but no changes were observed with phosphorylation status of FAK or MAPK. Importantly, knockdown of PEXpress significantly shortened the major axis of SC cells (p=0.0006), while knockdown of hnRNPL did not. In parallel experiments, we observed that PEXpress did not affect hnRNPL-mediated eNOS splicing (p=0.956 in HEK293 cells. Experiments examining PEXpress-mediation of CD44 splicing are underway.

Conclusions : PEXpress/hnRNPL directly regulates and is responsive to critical pathways of cellular adhesion and morphology in SC cells. PEXpress/hnRNPL complex represents a viable therapeutic target for treating PEXG.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×