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Open AccessJournal ArticleDOI

Cytochemical localization of endogenous peroxidase in thyroid follicular cells.

Judy M. Strum, +1 more
- 01 Mar 1970 - 
- Vol. 44, Iss: 3, pp 655-666
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TLDR
It is suggested that the microvillous apical cell border is the major site where iodination occurs and that apical vesicles also play a role in iodination, and the in vitro effect of cyanide, aminotriazole, and thiourea is also discussed.
Abstract
Endogenous peroxidase activity in rat thyroid follicular cells is demonstrated cytochemically. Following perfusion fixation of the thyroid gland, small blocks of tissue are incubated in a medium containing substrate for peroxidase, before being postfixed in osmium tetroxide, and processed for electron microscopy. Peroxidase activity is found in thyroid follicular cells in the following sites: (a) the perinuclear cisternae, (b) the cisternae of the endoplasmic reticulum, (c) the inner few lamellae of the Golgi complex, (d) within vesicles, particularly those found apically, and (e) associated with the external surfaces of the microvilli that project apically from the cell into the colloid. In keeping with the radioautographic evidence of others and the postulated role of thyroid peroxidase in iodination, it is suggested that the microvillous apical cell border is the major site where iodination occurs. However, that apical vesicles also play a role in iodination cannot be excluded. The in vitro effect of cyanide, aminotriazole, and thiourea is also discussed.

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Citations
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Journal ArticleDOI

The fine structural localization of endogenous and exogenous peroxidase activity in kupffer cells of rat liver

TL;DR: In 25–40% of sinusoidal cells, an electron-opaque reaction product is localized in segments of the endoplasmic reticulum, including the perinuclear cisternae, a few Golgi vesicles and saccules and in some large membrane-bounded granules.
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Mononuclear phagocytes (Kupffer cells) and endothelial cells. Identification of two functional cell types in rat liver sinusoids by endogenous peroxidase activity.

TL;DR: The peroxidase reaction distinguishes the typical mononuclear phagocytes or Kupffer cells of rat liver from the endothelial-lining cells, and the so-called fat-storing cells are per oxidase negative and totally nonphagocytic.
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Roles of hydrogen peroxide in thyroid physiology and disease

TL;DR: It is proposed that various pathologies can be explained, at least in part, by overproduction and lack of degradation of H2O2 (tumorigenesis, myxedematous cretinism, and thyroiditis) and by failure of the H 2O2 generation or its positive control system (congenital hypothyroidism).
Journal ArticleDOI

Cytochemical discrimination between catalases and peroxidases using diaminobenzidine

TL;DR: It is concluded that when cells are incubated without prior fixation, in a DAB medium at room temperature and pH 7.3 with 0.003% H2O2, peroxidases produce a visible cytochemical stain, while catalases do not; and Ultrastructural preservation is satisfactory in tissues incubated prior toxation.
Journal ArticleDOI

Biosynthesis of thyroid hormone: Basic and clinical aspects☆

TL;DR: Thyroid hormone formation requires the coincident presence of peroxidase, H2O2, iodide, and acceptor protein at one anatomic locus in the cell, and clinical problems involving defective per oxidase function are among the most frequent hereditary defects of thyroid hormone formation.
References
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Journal ArticleDOI

Improvements in epoxy resin embedding methods.

TL;DR: Epoxy embedding methods of Glauert and Kushida have been modified so as to yield rapid, reproducible, and convenientembedding methods for electron microscopy.
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A simplified lead citrate stain for use in electron microscopy.

TL;DR: This communication reports the use of a commercially available lead citratO to eliminate the lead citrate stain in electron microscopy.
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