4.7 Article

Diabetic cataract in the Nile grass rat: A longitudinal phenotypic study of pathology formation

Journal

FASEB JOURNAL
Volume 35, Issue 6, Pages -

Publisher

WILEY
DOI: 10.1096/fj.202100353R

Keywords

animal model; anterior; posterior subcapsular cataract (ASC; PSC); lens epithelial cells (LEC); metabolic syndrome (MetS); type 2 diabetes (T2D)

Funding

  1. NIH Impact Award [DK108238-01]
  2. JDRF Innovation award
  3. Malaysian Palm Oil Board (MPOB)

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This study conducted a longitudinal investigation into diabetic cataract in Nile grass rats, identifying various types of cataracts and elucidating the mechanisms underlying their development. The research offers insights into early stages of diabetic cataract and highlights the suitability of Nile grass rats as a model for mechanistic studies in the context of metabolism, diabetes, and aging.
Diabetes is a major risk factor for cataract, the leading cause of blindness worldwide. There is an unmet need for a realistic model of diabetic cataract for mechanistic and longitudinal studies, as existing models do not reflect key aspects of the complex human disease. Here, we introduce and characterize diabetic cataract in the Nile grass rat (NGR, Arvicanthis niloticus), an established model of metabolic syndrome and type 2 diabetes (T2D). We conducted a longitudinal study of cataract in over 88 NGRs in their non-diabetic, pre-diabetic, and diabetic stages of metabolism. Oral glucose tolerance test (OGTT) results distinguished the metabolic stages. Diverse cataract types were observed in the course of diabetes, including cortical, posterior subcapsular (PSC), and anterior subcapsular (ASC), all of which succeeded a characteristic dotted ring stage in all animals. The onset ages of diabetes and cataract were 44 +/- 3 vs 29 +/- 1 (P < .001) and 66 +/- 5 vs 58 +/- 6 (not significant) weeks in females and males, respectively. Histological analysis revealed fiber disorganization, vacuolar structures, and cellular proliferation and migration in cataractous lenses. The lens epithelial cells (LECs) in non-diabetic young NGRs expressed the stress marker GRP78, as did LECs and migrated cells in the lenses of diabetic animals. Elucidating mechanisms underlying LEC proliferation and migration will be clinically valuable in prevention and treatment of posterior capsule opacification, a dreaded complication of cataract surgery. Marked changes in N-cadherin expression emphasized a role for LEC integrity in cataractogenesis. Apoptotic cells were dispersed in the equatorial areas in early cataractogenesis. Our study reveals diverse cataract types that spontaneously develop in the diabetic NGR, and which uniquely mirror the cataract and its chronic course of development in individuals with diabetes. We provide mechanistic insights into early stages of diabetic cataract. These unique characteristics make NGR highly suited for mechanistic studies, especially in the context of metabolism, diabetes, and aging.

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