» Articles » PMID: 21846800

Melatonin Controls Photoperiodic Changes in Tanycyte Vimentin and Neural Cell Adhesion Molecule Expression in the Djungarian Hamster (Phodopus Sungorus)

Overview
Journal Endocrinology
Specialty Endocrinology
Date 2011 Aug 18
PMID 21846800
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

The Djungarian hamster displays photoperiodic variations in gonadal size synchronized to the seasons by the nightly secretion of the pineal hormone melatonin. In short photoperiod (SP), the gonads regress in size, and circulating sex steroids levels decline. Thus, the brain is subject to seasonal variations of both melatonin and sex steroids. Tanycytes are specialized glial cells located in the ependymal lining of the third ventricle. They send processes either to the meninges or to blood vessels of the medio-basal hypothalamus. Furthermore, they are known to locally modulate GnRH release in the median eminence and to display seasonal structural changes. Seasonal changes in tanycyte morphology might be mediated either through melatonin or sex steroids. Therefore, we analyzed the effects of photoperiod, melatonin, and sex steroids 1) on tanycyte vimentin expression by immunohistochemistry and 2) on the expression of the neural cell adhesion molecule (NCAM) and polysialic acid as markers of brain plasticity. Vimentin immunostaining was reduced in tanycyte cell bodies and processes in SP. Similarly, tanycytes and their processes contained lower amounts of NCAM in SP. These changes induced by SP exposure could not be restored to long photoperiod (LP) levels by testosterone supplementation. Likewise, castration in LP did not affect tanycyte vimentin or NCAM expression. By contrast, late afternoon melatonin injections mimicking a SP-like melatonin peak in LP hamsters reduced vimentin and NCAM expression. Thus, the seasonal changes in vimentin and NCAM expression in tanycytes are regulated by melatonin independently of seasonal sex steroid changes.

Citing Articles

Seasonal changes in activity of hypothalamic thyroid hormone system in different winter phenotypes of Djungarian hamster (Phodopus sungorus).

Przybylska-Piech A, Diedrich V, Herwig A PLoS One. 2024; 19(10):e0309591.

PMID: 39453953 PMC: 11508246. DOI: 10.1371/journal.pone.0309591.


Implications of Hypothalamic Neural Stem Cells on Aging and Obesity-Associated Cardiovascular Diseases.

Plakkot B, Di Agostino A, Subramanian M Cells. 2023; 12(5).

PMID: 36899905 PMC: 10000584. DOI: 10.3390/cells12050769.


Location of the Cell Adhesion Molecule "Coxsackievirus and Adenovirus Receptor" in the Adult Mouse Brain.

Wehbi A, Kremer E, Dopeso-Reyes I Front Neuroanat. 2020; 14:28.

PMID: 32581729 PMC: 7287018. DOI: 10.3389/fnana.2020.00028.


Photoperiodic and clock regulation of the vitamin A pathway in the brain mediates seasonal responsiveness in the monarch butterfly.

Iiams S, Lugena A, Zhang Y, Hayden A, Merlin C Proc Natl Acad Sci U S A. 2019; 116(50):25214-25221.

PMID: 31767753 PMC: 6911188. DOI: 10.1073/pnas.1913915116.


Nutrient Sensing by Hypothalamic Tanycytes.

Elizondo-Vega R, Recabal A, Oyarce K Front Endocrinol (Lausanne). 2019; 10:244.

PMID: 31040827 PMC: 6476911. DOI: 10.3389/fendo.2019.00244.