Cell-to-cell communication in the anterior pituitary: evidence for gap junction-mediated exchanges between endocrine cells and folliculostellate cells

• Published in: Endocrinology (Philadelphia) 1996-08, Vol.137 (8), p.3356-3367
• Main Authors: Morand, I, Fonlupt, P, Guerrier, A, Trouillas, J, Calle, A, Remy, C, Rousset, B, Munari-Silem, Y
• Format: Article
• Language: English
• Subjects: Adrenocorticotropic hormone; Animal tissues; Animals; Cell Communication; Cell differentiation; Cell interactions; Cells, Cultured; Communication; Connexin 43 - metabolism; Coupling; Cytoplasm; Endocrine Glands - cytology; Endocrine Glands - physiology; Fluorescence; Fluorescent Antibody Technique, Indirect; Fluorescent Dyes; Functionals; Gap junctions; Gap Junctions - physiology; Growth hormones; Hormones; Immunofluorescence; Isoquinolines; Luteinizing hormone; Male; Microinjection; Pituitary (anterior); Pituitary Gland, Anterior - cytology; Pituitary Gland, Anterior - metabolism; Pituitary Gland, Anterior - physiology; Proteins; Rats; Rats, Sprague-Dawley; S100 protein; S100 Proteins - metabolism
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.137.8.3356

The ability of rat anterior pituitary cells to communicate through gap junctions (GJ) was studied using a fluorescent molecule, Lucifer Yellow (LY), which freely passes through GJ channels. The probe was introduced into the cell cytoplasm by using either the cut-end loading method on intact tissue, or cell microinjection on cultured cells. The identification of communicating cells was performed by immunofluorescence labeling of specific hormones in endocrine cells and of S100 protein in folliculostellate (FS) cells. Rat anterior pituitary cells in their physiological organization, i.e. in the intact tissue, exhibited a high level of coupling through GJ. LY-labeled cells were found up to 300-microns apart from its site of introduction. The communicating cells were primarily PRL cells, GH cells, and FS cells. Only a few LH, TSH, and ACTH cells were labeled with LY. Anterior pituitary cells, isolated from the rat tissue by mild protease treatment and cultured for 3 days, reestablished functional GJ as demonstrated by microinjection of LY into individual cells. By immunolabeling of specific hormones and/or S100 protein, we found a GJ coupling between FS cells, and between FS cells and endocrine cells, including PRL cells. The communication between FS cells was by far the most frequent. In conclusion, we demonstrate the presence of functional GJ between anterior pituitary cells of the same type and between anterior pituitary cells having distinct differentiated functions.