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Simultaneous ultrastructural identification of growth hormone and its messenger ribonucleic acid using combined immunohistochemistry and non-radioisotopicin situ hybridization: A technical note
Authors:Akira Matsuno   Hirotoshi Utsunomiya   Yoshitaka Ohsugi   Susumu Takekoshi   Naoko Sanno   R. Yoshiyuki Osamura   Koichi Nagao   Akira Tamura  Tadashi Nagashima
Affiliation:(1) Department of Neurosurgery, Teikyo University Ichihara Hospital, 3426-3 Anegasaki, 299-01 Ichihara City, Chiba, Japan;(2) Department of Pathology, Tokai University School of Medicine, Boseidai, 259-11 Isehara City, Kanagawa, Japan;(3) Drug Safety, Laboratory, Taiho Pharmaceutical Co. Ltd., 224-2 Hiraishiebisuno, Kawauchi, 771-01 Tokushima City, Tokushima, Japan;(4) Department of Pathology, Teikyo University Ichihara Hospital, 3426-3 Anegasaki, 299-01 Ichihara City, Chiba, Japan;(5) Department of Neurosurgery, Teikyo University Hospital, 2-11-1 Kaga, Itabashi-ku, 173 Tokyo, Japan
Abstract:Summary The present electron microscopical study is concerned with the simultaneous visualization of messenger ribonucleic acid (mRNA) and its encoded protein in the same specimen. Pre-embedding electron microscopicalin situ hybridization (EM-ISH) on rat pituitary gland tissue localized growth hormone mRNA in the polysomes of the rough endoplasmic reticulum, and subsequent postembedding immunolabelling using protein A-colloidal gold particles identified growth hormone mainly in the secretory granules. We believe that our report provides the first simultaneous ultrastructural identification of mRNA and its encoded protein using combined pre-embedding EM-ISH and immunohistochemistry. In this method, the signals for mRNA were localized specifically as highly electron dense products on the polysomes of the endoplasmic reticulum, and those for its encoded protein were recognized as gold particles both in the cisternae of the reticulum and in the secretory granules. Our ultrastructural double labelling method for mRNA and protein may provide a tool to find important clues for elucidating the intracellular correlation of mRNA translation and secretion of translated protein, because of its high resolution, good morphological preservation, and the specific localization of the reaction products.
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