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Updated: May 29, 2026

Generation of Single-Cell Suspensions from Mouse Neural Tissue
Published on: July 7, 2009
Thyroid hormone and the neuroglia: both source and target.
Petra Mohácsik1, Anikó Zeöld, Antonio C Bianco
1Laboratory of Endocrine Neurobiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1083, Hungary.
Thyroid hormone activation in the brain relies on type 2 iodothyronine deiodinase (D2) in glial cells. This enzyme converts thyroxine to T3, impacting neuronal gene expression and brain function in health and disease.
Area of Science:
- Neuroscience
- Endocrinology
- Cell Biology
Background:
- Thyroid hormone is essential for nervous system development and function.
- Thyroxine requires brain conversion to the active form, triiodothyronine (T3), for nuclear receptor binding and gene regulation.
Purpose of the Study:
- To discuss the impact of thyroid hormone on glial cell function.
- To review the regulation of T3 generation by type 2 iodothyronine deiodinase (D2) in glial cells.
- To highlight the role of glial-neuronal interactions in thyroid hormone regulation.
Main Methods:
- Literature review on thyroid hormone action in the brain.
- Discussion of type 2 iodothyronine deiodinase (D2) activity in glial subtypes (astrocytes, tanycytes).
- Analysis of recent evidence on paracrine signaling from glial D2 to neurons.
Main Results:
- Type 2 iodothyronine deiodinase (D2) in glial cells (astrocytes, tanycytes) activates thyroxine to T3 in the brain.
- D2 activity is finely tuned in different glial subtypes, regulating local T3 generation.
- Glial D2 exerts paracrine effects on neuronal gene expression, emphasizing glial-neuronal communication.
Conclusions:
- Glial cells, particularly astrocytes and tanycytes, are critical for thyroid hormone activation in the brain via D2.
- The regulation of T3 generation by D2 in glial cells is a key mechanism controlling neuronal function.
- Glial-neuronal interactions mediated by D2 are fundamental to thyroid hormone signaling pathways in the brain, relevant to both normal function and disease states.
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