Knockdown of the thyroid hormone transporter MCT8 in chicken retinal precursor cells hampers early retinal development and results in a shift towards more UV/blue cones at the expense of green/red cones.

Thyroid hormones (THs) play a crucial role in coordinating brain development in vertebrates. They fine-tune processes like cell proliferation， migration， and differentiation mainly by regulating the transcriptional activity of many essential genes. Regulators of TH availability thereby define the cellular concentration of the bioactive 3，5，3'-triiodothyronine， which binds to nuclear TH receptors. One important regulator， the monocarboxylate transporter 8 (MCT8)， facilitates cellular TH uptake and is known to be necessary for correct brain development， but data on its potential role during retinal development is lacking. The retinal cyto-architecture has been conserved throughout vertebrate evolution， and we used the chicken embryo to study the need for MCT8 during retinal development. Its external development allows easy manipulation， and MCT8 is abundantly expressed in the retina from early stages onwards. We induced MCT8 knockdown by electroporating a pRFP-MCT8-RNAi vector into the retinal precursor cells (RPCs) at embryonic day 4 (E4)， and studied the consequences for early (E6) and late (E18) retinal development. The empty pRFP-RNAi vector was used as a control. RPC proliferation was reduced at E6. This resulted in cellular hypoplasia and a thinner retina at E18 where mainly photoreceptors and horizontal cells were lost， the two predominant cell types that are born around the stage of electroporation. At E6， differentiation into retinal ganglion cells and amacrine cells was delayed. However， since the proportion of a given cell type within the transfected cell population at E18 was similar in knockdown and controls， the partial loss of some cell types was most-likely due to reduced RPC proliferation and not impaired cell differentiation. Photoreceptors displayed delayed migration at first， but had successfully reached the outer nuclear layer at E18. However， they increasingly differentiated into short wavelength-sensitive cones at the expense of medium/long wavelength-sensitive cones， while the proportion of rods was unaltered. Improperly formed sublaminae in the inner plexiform layer additionally suggested defects in synaptogenesis. Altogether， our data echoes effects of hypothyroidism and the loss of some other regulators of TH availability in the developing zebrafish and rodent retina. Therefore， the expression of MCT8 in RPCs is crucial for adequate TH uptake during cell type-specific events in retinal development.