Phagocytotic removal of apoptotic endocrine cells by folliculostellate cells and its functional implications in clusterin accumulation in pituitary colloids in helmeted guinea fowl ( Numida meleagris)

• Published in: Acta histochemica 2006-01, Vol.108 (1), p.69-80
• Main Authors: Claudius, Luziga, Yoshimi, Yamamoto, Yoichiro, Horii, Gabriel, Mbassa, Koichi, Mamba
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Apoptosis - physiology; Clusterin - genetics; Clusterin - metabolism; Colloid; Colloids - chemistry; Folliculostellate cells; Galliformes - genetics; Galliformes - metabolism; Guinea fowl; Immunohistochemistry; In Situ Hybridization; Microscopy, Electron; Phagocytosis; Phagocytosis - physiology; Pituitary gland; Pituitary Gland, Anterior - cytology; Pituitary Gland, Anterior - metabolism; Pituitary Gland, Anterior - ultrastructure; RNA, Messenger - genetics; RNA, Messenger - metabolism; S100 Proteins - analysis
• ISSN: 0065-1281; 1618-0372
• DOI: 10.1016/j.acthis.2006.01.006

The different cell types in the anterior pituitary behave as dynamic populations. The gland maintains a continuous renewal of cells to ensure a dynamic balance between cell division, differentiation, growth arrest and apoptosis. Apoptosis is a frequent event in the anterior pituitary in which unwanted cells are eliminated without affecting neighboring cells. We examined the link between apoptosis and the occurrence of colloids in the guinea fowl ( Numida meleagris) pituitary gland and the relationship of clusterin accumulation in the colloids. S-100 positive folliculostellate (FS) cells were found surrounding colloids. Apoptotic cells detected by single stranded DNA (ssDNA) immunohistochemistry were observed in the whole anterior pituitary and preferentially near colloid masses. Clusterin protein was detected in endocrine cells, FS cells and in the colloids. In situ hybridization showed clusterin mRNA in endocrine cells and FS cells. Simultaneous localization was performed to determine whether clusterin mRNA and ssDNA within anterior pituitary was present within the same cell. Clusterin mRNA was not detected in apoptotic cells but was present in neighboring surviving cells. At the ultrastructural level, numerous endocrine cells at different stages of apoptosis were found phagocytosed by FS cells. Our results suggest that clusterin is produced by endocrine cells for cytoprotection before death. Apoptotic endocrine cells are phagocytosed by FS cells and digested by their lysosomal enzymes. In FS cells, clusterin interacts and aggregates with by-products of digestion that subsequently become stored in colloid as a residual body.