4.5 Article

Segmental outflow dynamics in the trabecular meshwork of living mice

Journal

EXPERIMENTAL EYE RESEARCH
Volume 225, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exer.2022.109285

Keywords

Trabecular meshwork; Segmental outflow; Mouse models; Aqueous humour outflow

Categories

Funding

  1. NIH [EY022359, EY033142]
  2. National Glaucoma Research
  3. Bright-Focus Foundation [G2006-057, G2011-020, G2020-003, G2021004F]

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In this study, the researchers investigated the segmental outflow patterns in the trabecular meshwork of living mice and their changes over time and with age. They found that these patterns are not static but redistribute over time, with an age-related decline in the rate of redistribution.
Aqueous humour does not drain uniformly through the trabecular meshwork (TM), but rather follows non-uniform or segmental routes. In this study, we examined whether segmental outflow patterns in the TM change over time in living mice and whether such changes are affected by age. Segmental outflow patterns were labelled by constant-pressure infusion of fluorescent tracer microparticles into the anterior chamber of anes-thetised C57BL/6J mice at 3 or 8 months of age. Two different tracer colours were infused at separate time points with an interval of Delta t = 0, 2, 7 or 14 days. In a separate experiment, one tracer was infused in vivo while the second tracer was infused ex vivo after 2 days. The spatial relationship between the two tracer patterns was analysed using the Pearson's correlation coefficient, r. In 3-month-old mice, there was a time-dependent decay in r, which was near unity at Delta t = 0 and near zero at Delta t = 14 days. In 8-month-old mice, r remained elevated for 14 days. Segmental outflow patterns measured in young mice ex vivo were not significantly different from those measured in vivo after accounting for the expected changes over 2 days. Therefore, segmental outflow patterns are not static in the TM but redistribute over time, achieving near complete loss of correlation by 2 weeks in young healthy mice. There is an age-related decline in the rate at which segmental outflow patterns redistribute in the TM. Further research is needed to understand the dynamic factors controlling segmental outflow.

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