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Related Concept Videos

T Cell Types and Functions01:24

T Cell Types and Functions

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When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
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Related Experiment Video

Updated: Aug 13, 2025

Assessment of Vascular Regeneration in the CNS Using the Mouse Retina
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IL-17A Enhances Retinal Neovascularization.

Brooklyn E Taylor1, Chieh A Lee1, Thomas E Zapadka1,2

  • 1Department of Ophthalmology and Visual Science, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

International Journal of Molecular Sciences
|January 21, 2023
PubMed
Summary
This summary is machine-generated.

Interleukin-17A (IL-17A) drives retinal neovascularization in ocular diseases like diabetic retinopathy. Targeting IL-17A may offer new therapies for vision loss caused by retinal angiogenesis.

Keywords:
IL-17Aneovascularizationretina

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Area of Science:

  • Ophthalmology
  • Immunology
  • Vascular Biology

Background:

  • Retinal neovascularization is a major cause of vision loss in diseases such as diabetic retinopathy.
  • Interleukin-17A (IL-17A) is implicated in non-proliferative diabetic retinopathy, but its role in proliferative stages was unclear.

Purpose of the Study:

  • To investigate the role of IL-17A in vascular angiogenesis and neovascularization in the retina.
  • To determine if IL-17A contributes to the development of proliferative diabetic retinopathy.

Main Methods:

  • Assessed IL-17A's effect on vascular endothelial growth factor (VEGF) production in retinal cells.
  • Examined IL-17A's impact on retinal endothelial cell proliferation and VEGF-dependent angiogenesis.
  • Utilized an oxygen-induced retinopathy model to study IL-17A's role in retinal neovascularization.

Main Results:

  • Diabetes-mediated IL-17A enhances VEGF production in retinal cells, Muller glia, and endothelial cells.
  • IL-17A promotes retinal endothelial cell proliferation and VEGF-driven vascular angiogenesis.
  • IL-17A significantly increases retinal neovascularization in an oxygen-induced retinopathy model.

Conclusions:

  • IL-17A plays a critical role in retinal vascular proliferation and neovascularization.
  • IL-17A represents a potential therapeutic target for treating blinding ocular neovascular diseases.