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Open AccessJournal ArticleDOI

Proliferative behavior of differentiating cells in the developing rat parotid gland.

Robert S. Redman, +1 more
- 01 Jul 1970 - 
- Vol. 46, Iss: 1, pp 81-87
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TLDR
Data suggest that the acinar cells of the rat parotid gland comprise an expanding cell population, and support the view that the division of cells in advanced stages of differentiation may be important in the growth of certain organs and tissues.
Abstract
Parotid glands of litters of rats at age intervals from 20 days in utero to 100 days were assayed for DNA content and examined by light- and electron-microscopy. The age differences in total DNA and DNA concentration indicated that there was a rapid rate of proliferation of parenchymal cells until 25 postnatal days, after which the rate declined rapidly, and that there was a rapid increase in cell size between 18 and 25 days. These findings were substantiated by histologic observations, such as the presence of numerous mitotic figures until 25 days of age, and the rapid maturation of the acinar cells between 18 and 25 days. These data suggest that the acinar cells of the rat parotid gland comprise an expanding cell population. Light- and electron-microscopic observations consistently indicated that cells with mitotic figures were about as well differentiated as other parenchymal cells at all stages of gland development, including mature acinar cells observed at ages 23 and 25 days. These observations support the view that the division of cells in advanced stages of differentiation may be important in the growth of certain organs and tissues.

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Citations
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Journal ArticleDOI

An ultrastructural analysis of the developing embryonic pancreas

TL;DR: The morphological observations of this study are consistent with the previously proposed biphasic model of differentiation for the exocrine and endocrine B cells, and the development of specific organelles correlates with the pattern of accumulation of the specific exocrine proteins and insulin.
Book ChapterDOI

Interrelations of the proliferation and differentiation processes during cardiact myogenesis and regeneration.

TL;DR: The chapter describes the complicated proliferative behavior of cardiac-muscle cells both in normal myogenesis and regeneration and its dependence on the differentiative properties of these cells.
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Salivary glands: a paradigm for diversity of gland development.

TL;DR: The origins of the salivary glands are examined by reviewing the expression patterns of several genes with known morphogenetic potential that may be involved based on developmental timing and location and the possibility that factors leading to determination of the sites of mammalianSalivary gland development might be homologous to the regulatory cascade leading to salivARY gland formation in Drosophila is evaluated.
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Salivary Gland Homeostasis Is Maintained through Acinar Cell Self-Duplication

TL;DR: The results support a revised model for salivary gland homeostasis based predominantly on self-duplication of acinar cells, rather than on differentiation of stem cells.
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Mitosis in rat thyroid epithelial cells in vivo: I. Ultrastructural changes in cytoplasmic organelles during the mitotic cycle

TL;DR: The ultrastructure of mitosis was studied in polarized, well-differentiated thyroid epithelial cells in vivo following stimulation with the goitrogen, thiouracil, and attention was focused on changes occurring in cytoplasmic organelles.
References
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A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid

TL;DR: The present study arose from the observation that a more intense colour was sometimes produced if, instead of being heated at 1000 for 10 min., the reaction mixture was allowed to stand overnight at room temperature.
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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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Staining of Tissue Sections for Electron Microscopy with Heavy Metals

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Embedding in epoxy resins for ultrathin sectioning in electron microscopy.

TL;DR: More rapid than previous techniques, this method gives blocks which do not fracture unduly on trimming and provides sections of soft tissues at 1 μ for phase contrast microscopy, as well as ultrathin sections which cut as easily with glass knives as sections of methacrylate.
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