| Literature DB >> 35852615 |
Svein Achicallende1,2, Itziar Bonilla-Del Río1,2, Maitane Serrano1,2, Amaia Mimenza1,2, Leire Lekunberri1,2, Ilazki Anaut-Lusar1,2, Nagore Puente1,2, Inmaculada Gerrikagoitia3,4, Pedro Grandes5,6.
Abstract
The cannabinoid CB1 receptor-mediated functions in astrocytes are highly dependent on the CB1 receptor distribution in these glial cells relative to neuronal sites, particularly at the nearby synapses under normal or pathological conditions. However, the portrait of the CB1 receptor distribution in astroglial compartments remains uncompleted because of the scarce CB1 receptor expression in these cells and the limited identification of astrocytes. The glial fibrillary acidic protein (GFAP) is commonly used as astroglial marker. However, because GFAP is a cytoskeleton protein mostly restricted to the astroglial cell bodies and their main branches, it seems not ideal for the localization of CB1 receptor distribution in astrocytes. Therefore, alternative markers to decipher the actual astroglial CB1 receptors are required. In this work, we have compared the glutamate aspartate transporter (GLAST) versus GFAP for the CB1 receptor localization in astrocytes. We found by immunoelectron microscopy that GLAST reveals almost three-fold astroglial area and four-fold astroglial membranes compared to GFAP. In addition, this better visualization of astrocytes was associated with the detection of 12% of the total CB1 receptor labeling in GLAST-positive astrocytes.Entities:
Keywords: Electron microscopy; Endocannabinoid system; Glia; Glial markers; Hippocampus; Immunocytochemistry
Year: 2022 PMID: 35852615 DOI: 10.1007/s00418-022-02139-4
Source DB: PubMed Journal: Histochem Cell Biol ISSN: 0948-6143 Impact factor: 2.531