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Expression of Brain-Derived Neurotrophic Factor and Its Receptors in the Median Eminence Cells with Sensitivity to Stress

Cerebral Plasticity Laboratory (L.G., S.A., L.T.-A.), Formation de Recherche en Evolution-2693 Centre National de la Recherche Scientifique, University of Montpellier II, 34095 Montpellier, France; and Biology of Endocrine Neurons Laboratory (G.A.), Unité Mixte de Recherche 5101 Centre National de la Recherche Scientifique, Center of Pharmacology and Endocrinology, 34094 Montpellier, France

Address all correspondence and requests for reprints to: Dr. Lucia Tapia-Arancibia, Cerebral Plasticity Laboratory, Formation de Recherche en Evolution-2693 Centre National de la Recherche Scientifique, University of Montpellier 2, Place Eugène Bataillon, 34095 Montpellier, France. E-mail: aranci{at}univ-montp2.fr.

The median eminence (ME) is considered as the final common pathway connecting the nervous and endocrine systems. In this neurohemal structure, dynamic interactions among nerve terminals, tanycytes, and astrocytes determine through plastic processes the neurohormones access to the portal blood. Because brain-derived neurotrophic factor (BDNF) is involved in plastic changes, we investigated its presence and that of its receptors (TrkB) in the different cellular types described in the ME. Using in situ hybridization and immunohistochemical techniques, we demonstrated that BDNF immunoreactivity was essentially located in the astrocytes and to a lesser extent in tanycytes. By contrast, BDNF was not detected in nerve terminals reaching the external layer of the ME. TrkB antibodies recognizing the extracellular receptor domain labeled all of these different cell types, suggesting an autocrine or paracrine action of BDNF at this level. More selective antibodies showed that TrkB.FL immunostaining was found in tanycytes and nerve endings, whereas TrkB.T1 immunostaining was localized in all cellular types. Immobilization stress increased BDNF mRNA and BDNF immunoreactivity patterns and induced biphasic BDNF release from the ME, as analyzed by push-pull perfusion. In addition, we observed that 60-min stress intensified BDNF immunoreactivity in the internal layer and also its colocalization with glial fibrillary acidic protein. Stress also accentuated BDNF immunostaining in the perivascular space in elements that were not labeled with antibodies recognizing fibroblast or endothelial cells. These data disclosed a novel location of BDNF and its receptors in the ME, which are presumably involved in dynamic processes such as hormone release.

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