Modulation of factors affecting optic nerve head astrocyte migration

Haixi Miao, Andrea W. Crabb, M. Rosario Hernandez, Thomas J. Lukas

Research output: Contribution to journalArticlepeer-review

23 Scopus citations


PURPOSE. The authors investigated the role of myosin light chain kinase (MYLK) and transforming growth factor beta (TGFβ) receptor pathways in optic nerve head (ONH) astrocyte migration. They further investigated how the expression of these genes is altered by elevated hydrostatic pressure (HP). METHODS. PCR was used to determine the isoforms of MYLK expressed in ONH astrocytes. siRNAs against MYLK (all isoforms) and TGFβ receptor 2 (TGFBR2) were prepared and tested for effects on the migration of cultured ONH astrocytes. Finally, the effects of elevated HP (24-96 hours) on the expression of MYLK isoforms and selected TGFβ pathway components were measured. RESULTS. Multiple isoforms of MYLK are present in ONH astrocytes from Caucasian (CA) and African American (AA) donors. Both populations express the short form (MYLK-130) and the long form (MYLK-210) of MYLK and a splicing variant within MYLK-210. MYLK-directed siRNA decreased MYLK expression and cell migration compared with control siRNA. siRNA directed against TGFβ receptor 2 also decreased cell migration compared with control and decreased extracellular matrix genes regulated by TGFβ signaling. Elevated HP increased the expression of MYLK-130 and MYLK-210 in both populations of astrocytes. However, TGFβ2 was uniquely upregulated by exposure to elevated HP in CA compared with AA astrocytes. CONCLUSIONS. Differential expression of TGFβ pathway genes and MYLK isoforms observed in populations of glaucomatous astrocytes applies to the elevated HP model system. MYLK may be a new target for intervention in glaucoma to alter reactive astrocyte migration in the ONH.

Original languageEnglish (US)
Pages (from-to)4096-4103
Number of pages8
JournalInvestigative Ophthalmology and Visual Science
Issue number8
StatePublished - Aug 2010

ASJC Scopus subject areas

  • Sensory Systems
  • Cellular and Molecular Neuroscience
  • Ophthalmology


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