Immunoreactive Pit-1 Protein in Hyperplastic Pars Intermedia Induced by Calcitonin of the Rat Pituitary Gland

Endocrine Journal

R. YOSHIYUKI OSAMURA¹  REIKO KUROTANI¹  MASANORI MURAKOSHI²  TAKAHARU NAKAYAMA²  RIE IKEDA²  TOSHI HORIUCHI² 

[1] Department of Pathology, Tokai University School of Medicine;Safety Research Department, Teikoku Hormone Mfg. Co., Ltd

关键词: Calcitonin;    Pituitary gland;    Alpha-subunit;    Pit-1;    Rat;   

DOI  :  10.1507/endocrj.47.13

学科分类：内分泌与代谢学

来源: Japan Endocrine Society

【 摘 要 】

References(27)Cited-By(1)To elucidate the effects of synthetic salmon calcitonin (sCT) on the cells in the rat pituitary gland, we histopathologically and immunohistochemically examined the early changes after 4 or 13 weeks treatment with sCT 120IU/kg. Focal proliferative lesions of the anterior pituitary glands were consistently found after treatment with sCT for 13 weeks. Histologically, the cells with the focal proliferative lesions were classified into the following three groups: 1) enlarged basophilic cell focus, 2) vacuolated cell focus and 3) chromophobe cell focus. These focal proliferative lesions had positive staining only for the alpha-subunit and failed to show Pit-1 protein immunoreactivity. The sCT treatment also increased the thickness of the pars intermedia. Hypertrophy of the pars intermediate cells was characteristically seen. Furthermore, Pit-1 protein immunoreactivity was clearly detected in the nuclei of the hyperplastic pars intermediate cells. All pars intermediate cells were equally stained by alpha- or beta-MSH and beta-endorphin in both vehicle- and sCT-treatment. No difference was seen. These findings strongly suggest a very close relationship between Pit-1 protein immunoreactivity and cellular proliferation induced by sCT.

【 授权许可】

Unknown