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Título

Thyroid Hormone Transporters MCT8 and OATP1C1 Are Expressed in Projection Neurons and Interneurons of Basal Ganglia and Motor Thalamus in the Adult Human and Macaque Brains

AutorWang, Tin; Wang, Yu; Montero-Pedrazuela, Ana CSIC ORCID ; Prensa, L.; Guadaño-Ferraz, Ana CSIC ORCID ; Rausell, Estrella
Palabras claveThyroid hormones
Thyroid hormone transporters
MCT8
OATP1C1
Human
Monkey
Basal ganglia
Motor thalamus
MSN cells
Nucleus basalis of Meynert
Fecha de publicación2023
EditorMultidisciplinary Digital Publishing Institute
CitaciónInternational Journal of Molecular Sciences 24(11): 9643 (2023)
ResumenMonocarboxylate transporter 8 (MCT8) and organic anion-transporting polypeptide 1C1 (OATP1C1) are thyroid hormone (TH) transmembrane transporters relevant for the availability of TH in neural cells, crucial for their proper development and function. Mutations in MCT8 or OATP1C1 result in severe disorders with dramatic movement disability related to alterations in basal ganglia motor circuits. Mapping the expression of MCT8/OATP1C1 in those circuits is necessary to explain their involvement in motor control. We studied the distribution of both transporters in the neuronal subpopulations that configure the direct and indirect basal ganglia motor circuits using immunohistochemistry and double/multiple labeling immunofluorescence for TH transporters and neuronal biomarkers. We found their expression in the medium-sized spiny neurons of the striatum (the receptor neurons of the corticostriatal pathway) and in various types of its local microcircuitry interneurons, including the cholinergic. We also demonstrate the presence of both transporters in projection neurons of intrinsic and output nuclei of the basal ganglia, motor thalamus and nucleus basalis of Meynert, suggesting an important role of MCT8/OATP1C1 for modulating the motor system. Our findings suggest that a lack of function of these transporters in the basal ganglia circuits would significantly impact motor system modulation, leading to clinically severe movement impairment.
Versión del editorhttp://dx.doi.org/10.3390/ijms24119643
URIhttp://hdl.handle.net/10261/341259
DOI10.3390/ijms24119643
ISSN1661-6596
E-ISSN1422-0067
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