Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Analysis of Sclera Macrophages in a Mouse Glaucoma Model
Author Affiliations & Notes
  • Maru Ando
    Johns Hopkins University, Baltimore, Maryland, United States
    Johns Hopkins University Center for Nanomedicine, Baltimore, Maryland, United States
  • Shiraj Crowdhury
    Johns Hopkins University, Baltimore, Maryland, United States
    Johns Hopkins University Center for Nanomedicine, Baltimore, Maryland, United States
  • Annie Mozzer
    Johns Hopkins University Center for Nanomedicine, Baltimore, Maryland, United States
  • Joe Gerald Jesu Raj
    Johns Hopkins University Center for Nanomedicine, Baltimore, Maryland, United States
  • Ian Pitha
    Johns Hopkins University Center for Nanomedicine, Baltimore, Maryland, United States
    Department of Ophthalmology, Johns Hopkins Medicine, Baltimore, Maryland, United States
  • Footnotes
    Commercial Relationships   Maru Ando None; Shiraj Crowdhury None; Annie Mozzer None; Joe Gerald Jesu Raj None; Ian Pitha None
  • Footnotes
    Support  Masason Foundation Research Grant
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 577. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Maru Ando, Shiraj Crowdhury, Annie Mozzer, Joe Gerald Jesu Raj, Ian Pitha; Analysis of Sclera Macrophages in a Mouse Glaucoma Model. Invest. Ophthalmol. Vis. Sci. 2024;65(7):577.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : Macrophages play an important role in wound healing and can influence fibroblast behavior. Previous studies have shown that mouse and human sclera contain macrophage populations. Here we investigate scleral macrophage markers in a mouse glaucoma model.

Methods : OHT was induced in C57BL/6J mice (3 months) by anterior chamber bead-injection (BI) and intraocular pressure (IOP) was monitored serially in OHT and control eyes by rebound tonometry (TonoLab, TioLat, Inc., Helsinki, Finland) at 1, 3, 7, 14, and 21 days after injection. Glaucomatous eyes were only included if IOP elevation was >7 mmHg compared to fellow eye control at 1, 3, or 7 days after BI. Mice were euthanized, eyes enucleated and cryopreserved at 3 days and 6 weeks after BI. Scleral eye cups were dissected and cross-sections from the posterior to segments of the eye were processed for immunolabelling with macrophage markers (CD68, CD11b, CD38, F4/80, and CD163) were used to characterize macrophage populations within the peripapillary sclera (PPS) and scleral cross-sections of the mouse eye.

Results : F4/80, CD68, CD11b, CD163, and CD38 positive cells were detected in the PPS and peripheral sclera of non-glaucomatous mice. CD11b positive cells were seen in the optic nerve, peripapillary sclera, and concentrated in the anterior and posterior sclera in the outer sclera layers and episcleral in non-glaucomatous mice. Following BI OHT for 6 weeks, there was an observable increase in strongly positive CD68 and CD11b cells in PPS and peripheral sclera. Three-day BI OHT eyes also had an increase in CD11b positive cells in the PPS.

Conclusions : This study shows multiple macrophage markers are present in peripheral and peripapillary region of sclera with an increase in CD11b for 3 days and 6 weeks, and an increase in CD68 for 6 weeks after IOP elevation. These results provide basis for future studies to understand the role of scleral macrophages in glaucoma.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

×
×

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.

×