The Neuronal Growth-Associated Protein (GAP)-43 Is Expressed by Corticotrophs in the Rat Anterior Pituitary After Adrenalectomy
Autor: | Charles M. Paden, John A. Watt, Harwood J. Cranston, Courtney L. Paterson, Tiffany H. Selong |
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Rok vydání: | 2006 |
Předmět: |
Male
medicine.medical_specialty Immunoelectron microscopy Immunocytochemistry Pituitary-Adrenal System Rats Sprague-Dawley GAP-43 Protein Endocrinology Adrenocorticotropic Hormone Anterior pituitary Pituitary Gland Anterior Internal medicine medicine Animals Tissue Distribution RNA Messenger Gap-43 protein Cellular localization Neurons biology Adrenalectomy Immunogold labelling Rats medicine.anatomical_structure biology.protein Corticotropic cell hormones hormone substitutes and hormone antagonists Endocrine gland |
Zdroj: | Endocrinology. 147:952-958 |
ISSN: | 1945-7170 0013-7227 |
DOI: | 10.1210/en.2005-0715 |
Popis: | The neuronal growth-associated protein (GAP)-43 has been localized in both long fibers and punctate clusters by immunocytochemistry within the rat anterior pituitary (AP). After adrenalectomy (ADX), GAP-43 immunoreactivity (GAP-43-ir) is greatly increased and is associated with corticotrophs at the light microscopic level. We have undertaken an electron microscopic study to determine the cellular localization of GAP-43 in the post-ADX AP. Using preembedding immunocytochemistry, we found GAP-43-ir localized exclusively to the cytoplasmic surface of the plasmalemma within a subset of endocrine cells with ultrastructure typical of degranulated corticotrophs at 4 d after ADX. We combined preembedding immunoelectron microscopy for GAP-43 with immunogold labeling for ACTH and found that GAP-43-ir was invariably present only in cells containing ACTH-positive granules. The density of GAP-43-ir was highest within extensive processes emanating from the soma, suggesting that these processes are the basis for the punctate clusters of GAP-43 staining seen surrounding corticotrophs in the light microscope. We also observed rare synaptic-like contacts between GAP-43-ir processes and distant cell bodies. GAP-43 mRNA was detected in extracts of the AP 4 d after ADX using RT-PCR, and quantitative PCR confirmed that GAP-43 mRNA was significantly up-regulated in the AP in response to ADX. We postulate that increased expression of GAP-43 may stimulate process outgrowth and intercellular communication by activated corticotrophs. |
Databáze: | OpenAIRE |
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