TSH enhances neurite outgrowth.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2024
Historique:
received: 12 07 2024
accepted: 24 09 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 1 11 2024
Statut: epublish

Résumé

Extra-thyroidal effects of TSH have been reported in various tissues expressing the TSH receptor (TSHR) including several areas of the brain. However, the influence of TSH on neuronal phenotypes has not been examined. Using a well-characterized human neuroblastoma cell line (SH-SY5Y), we have examined TSH signaling effects on the phenotype of these cells after their neuronal differentiation. Following an 18-day differentiation protocol, we successfully redifferentiated the SH-SY5Y cells into ~100% neuronal cells as indicated by the development of extensive neurofilaments with SMI-31 expression. Furthermore, using absolute digital PCR, we quantified TSHR mRNA, and also TSHR protein expression, in the redifferentiated cells and found that the neuronal cells expressed high quantities of both TSHR message and protein at baseline. Exposure to TSH induced primary, secondary, and tertiary neurite outgrowths, which are essential for cell-cell communication. Quantitative analysis of neurites using ImageJ showed a dose-dependent increase in neurites. The addition of TSH up to 1 mU/ml resulted in a ~2.5-fold increase in primary, and ~1.5-fold in secondary and tertiary neurites. The lengths of the neurites remained unaffected with the dosage of TSH treatment. Furthermore, TSHR signaling in the differentiated cells resulted in enhanced generation of cAMP, pPI3K, pAKT, and pNFkB pathways and suppression of pMAPK suggesting an influence of these signals in driving neurite outgrowth. These data showed that the TSH/TSHR axis in neurons may contribute to enhanced neurite outgrowth. The potential pathophysiological effects of TSH on the induction of neurite outgrowth and its relationship to neurodegenerative diseases remain to be explored.

Identifiants

pubmed: 39483982
doi: 10.3389/fendo.2024.1463964
pmc: PMC11524836
doi:

Substances chimiques

Thyrotropin 9002-71-5
Receptors, Thyrotropin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1463964

Informations de copyright

Copyright © 2024 Mansoori, Latif, Morshed, Zaidi and Davies.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Maryam Mansoori (M)

Thyroid Research Unit, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Rauf Latif (R)

Thyroid Research Unit, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Department of Medicine, James J. Peters VA Medical Center, New York, NY, United States.

Syed A Morshed (SA)

Thyroid Research Unit, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Department of Medicine, James J. Peters VA Medical Center, New York, NY, United States.

Mone Zaidi (M)

Center for Translational Medicine and Pharmacology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Terry F Davies (TF)

Thyroid Research Unit, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Department of Medicine, James J. Peters VA Medical Center, New York, NY, United States.

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Classifications MeSH