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Association of Centrioles with Clusters of Apical Vesicles in Mitotic Thyroid Epithelial Cells. Are Centrioles Involved in Directing Secretion?

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Journal Cell Tissue Res
Date 1979 Sep 2
PMID 527009
Citations 4
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Abstract

The ultrastructure of thyroid epithelial cells in mitosis has been investigated. A spatial association is described between clusters of apical vesicles (believed to contain thyroglobulin destined for secretion into the follicular lumen) and centrioles, in late prophase and late telophase cells. Quantitative techniques demonstrate the statistical significance of this association and suggest that it is not related to proximity of the Golgi apparatus or to the location of the centriole in the cell, which changes considerably during these phases of mitosis. The physical basis for this association remains uncertain, but microtubules emanating from the pericentriolar area may be involved. In interphase cells, centrioles are located very close to the follicular lumen, where the majority of apical vesicles are also found. The association of centrioles with clusters of apical vesicles also in mitotic cells suggests that in interphase cells the apically located centrioles may serve as a focus for apical vesicles, helping to direct these secretory vesicles toward the follicular lumen and to maintain cellular polarization. Previous studies demonstrating that centrioles can act as microtubule organizing centers in interphase cells and studies linking microtubules and secretion also tend to support this hypothesis.

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References
1.
Tamarin A, SREEBNY L . The rat submaxillary salivary gland. A correlative study by light and electron microscopy. J Morphol. 1965; 117(3):295-352. DOI: 10.1002/jmor.1051170303. View

2.
Zeligs J, Wollman S . Mitosis in rat thyroid epithelial cells in vivo. II. Centrioles and pericentriolar material. J Ultrastruct Res. 1979; 66(2):97-108. DOI: 10.1016/s0022-5320(79)90127-8. View

3.
Moe H, Mikkelsen H . Light microscopical and ultrastructural observations on the effect of vinblastine on ameloblasts of rat incisors in vivo. I. Short-term effect on secretory ameloblasts. Acta Pathol Microbiol Scand A. 1977; 85A(1):73-88. DOI: 10.1111/j.1699-0463.1977.tb03870.x. View

4.
REAVEN E, Reaven G . Distribution and content of microtubules in relation to the transport of lipid. An ultrastructural quantitative study of the absorptive cell of the small intestine. J Cell Biol. 1977; 75(2 Pt 1):559-72. PMC: 2109932. DOI: 10.1083/jcb.75.2.559. View

5.
Muller P, Rossignol B . Microtubules and protein secretion in rat lacrimal glands. Relationship between colchicine binding and its inhibitory effect on the intracellular transport of proteins. J Biol Chem. 1978; 253(11):3870-6. View