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Crinophagy in Thyroid Follicular and Parafollicular Cells of Male Obese Zucker Rat

机译:肥胖男性祖克大鼠甲状腺滤泡和滤泡旁细胞的吞噬

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Comparison between lean (Fa/?) and obese (fa/fa) young adult male Zucker rat thyroids reveals that obese rats display larger clusters of parafollicular cells than the lean ones with a lesser blood supply. Fa/? thyroid typically shows single or "twin'' C cells in follicles; fa/fa parafollicular cells appear with three functional aspects. Crinophagy is found in the fa/fa C cells amassing numerous aberrant calcitonin-containing vesicles among which lysosomes build these autophagic bodies by capturing vesicle contents, other organelles and, fusing with each other, increase their size. Other C cells contain many secretory vesicles but show few or no crinophagic structures. Another parafollicular cell type is revealed with scant organelles and highly contrasted secretory vesicles, different from calcitonin. Hypercalcemia of fa/fa rats corresponds to increased C cells population with accrued calcitonin production but a low calcitonin plasma level - verified by others - is likely caused by crinophagy of the altered vesicles. In addition, the T thyrocytes of fa/fa rats exhibit crinophagy bodies; this can confirm their hypothyroidism. Possibly, the known leptin mutation along with other unknown paracrine secretions alter both T and C thyrocytes' functions of the fa/fa rats, allowing high intracellular calcium and lower pH favoring autophagocytosis. Other longitudinal, interdisciplinary studies should further clarify the complex paracrine interactions existing between these endocrine structures because this animal model could be useful to understand human defects, such as the metabolic syndrome that involves obesity, cardiovascular, renal, hepatic, non-insulin dependent diabetes mellitus (NIDDM), hypothyroidism defects, as well as the etiology of thyroid medullary tumors.
机译:瘦鼠(Fa /?)与肥胖(fa / fa)的成年雄性Zucker大鼠甲状腺之间的比较表明,肥胖大鼠的卵泡旁细胞簇比贫血的大鼠少。 F A/?甲状腺通常在卵泡中显示单个或“双胞胎” C细胞; fa / fa滤泡旁细胞的出现具有三个功能方面;在fa / fa C细胞中发现吞噬,聚集了大量含有降钙素的异常囊泡,其中溶酶体通过这些溶酶体来构建这些自噬体。捕获小泡内容物,其他细胞器并相互融合,增加其大小;其他C细胞含有许多分泌性小泡,但几乎没有或没有眼相结构;另一种滤泡旁细胞类型的细胞器少且分泌对比强烈,不同于降钙素fa / fa大鼠的高钙血症与降钙素产生的C细胞数量增加相对应,但降钙素血浆水平较低(已被其他研究证实),可能是由于改变了囊泡的吞噬作用所致。可能是已知的瘦素突变以及其他未知蛋白ine的分泌会改变fa / fa大鼠的T和C甲状腺细胞功能,从而允许较高的细胞内钙和较低的pH值,有利于自噬。其他纵向,跨学科研究应进一步阐明这些内分泌结构之间存在的复杂旁分泌相互作用,因为这种动物模型可能有助于理解人类的缺陷,例如涉及肥胖,心血管,肾脏,肝脏,非胰岛素依赖型糖尿病的代谢综合征(NIDDM),甲状腺功能低下的缺陷以及甲状腺髓样肿瘤的病因。

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