Abstract

Thyroid hormones (THs) are important metabolic, growth, and differentiation regulators. As amphipathic ligands, TH access to target cells is limited by specific transporters. MCT8 is a high-affinity, bidirectional transporter of thyroid hormone. However, the role of Mct8 during adrenal development is not well understood. The adrenal cortex is a hormone-sensitive organ that experiences dramatic postnatal remodeling in rodents, with the transient X-zone regressing in males and persisting in females. This study aimed to characterize the spatial and temporal expression of Mct8 in development and determine whether post-weaning exogenous T3 alters this expression. Male and female wild-type (WT) and Mct8 knockout (Mct8KO) adrenal glands were harvested at postnatal days (P) 7, 14, 21, and 35. Mct8 mRNA abundance was determined by qRT-PCR. Hematoxylin staining was used to visualize adrenal morphology. Spatial localization of Mct8 expression was confirmed using the LacZ reporter of the Mct8 locus. Additional male and female mice were treated with T3 from P21-P35 to determine the effect of excess thyroid hormone on adrenal structure and Mct8 levels. The adrenal expression of Mct8 followed a biphasic developmental trajectory, with an initial peak in expression at P7, a gradual decrease in expression through P21, and a second, less substantial increase by P35. LacZ analysis revealed Mct8 promoter activity was spatially restricted to the inner cortex and medulla, and this persisted in females but was lost in males after X-zone regression. The persistence of the X-zone in T3-treated mice, regardless of genotype, further supports the idea that thyroid hormone signaling can influence adrenal structure through both Mct8-dependent and independent pathways, potentially involving efflux mechanisms. However, additional functional studies are needed to confirm these mechanisms.

Advisor

David Sharlin

Committee Member

Allison Land

Committee Member

Keenan Hartert

Date of Degree

2025

Language

english

Document Type

Thesis

Degree

Master of Science (MS)

Program of Study

Biology

Department

Biological Sciences

College

Science, Engineering and Technology

Available for download on Wednesday, December 15, 2027

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Rights Statement

In Copyright