The Immediate Early Response of Lens Epithelial Cells to Lens Injury

Cells. 2022 Nov 1;11(21):3456. doi: 10.3390/cells11213456.

Abstract

Cataracts are treated by lens fiber cell removal followed by intraocular lens (IOL) implantation into the lens capsule. While effective, this procedure leaves behind numerous lens epithelial cells (LECs) which undergo a wound healing response that frequently leads to posterior capsular opacification (PCO). In order to elucidate the acute response of LECs to lens fiber cell removal which models cataract surgery (post cataract surgery, PCS), RNA-seq was conducted on LECs derived from wild type mice at 0 and 6 h PCS. This analysis found that LECs upregulate the expression of numerous proinflammatory cytokines and profibrotic regulators by 6 h PCS suggesting rapid priming of pathways leading to inflammation and fibrosis PCS. LECs also highly upregulate the expression of numerous immediate early transcription factors (IETFs) by 6 h PCS and immunolocalization found elevated levels of these proteins by 3 h PCS, and this was preceded by the phosphorylation of ERK1/2 in injured LECs. Egr1 and FosB were among the highest expressed of these factors and qRT-PCR revealed that they also upregulate in explanted mouse lens epithelia suggesting potential roles in the LEC injury response. Analysis of lenses lacking either Egr1 or FosB revealed that both genes may regulate a portion of the acute LEC injury response, although neither gene was essential for expression of either proinflammatory or fibrotic markers at later times PCS suggesting that IETFs may work in concert to mediate the LEC injury response following cataract surgery.

Keywords: cataract surgery; immediate early genes; inflammation; lens; wound healing.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Capsule Opacification* / metabolism
  • Cataract Extraction*
  • Epithelial Cells / metabolism
  • Eye Injuries* / metabolism
  • Fibrosis
  • Lens Capsule, Crystalline* / metabolism
  • Lens Capsule, Crystalline* / pathology
  • Lens, Crystalline* / metabolism
  • Mice
  • Transcription Factors / metabolism

Substances

  • Transcription Factors