The thyroid angiofollicular units, a biological model of functional and morphological integration.

I Colin, A-C Gérard
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Abstract

The fundamental role of the thyroid gland is to ensure the biosynthesis of thyroid hormones whose primary role during embryonic development and the maintenance of homeostasis after birth is well known. The challenge here is double, as the hormone synthesis depends on both potentially toxic biochemical processes, as long as they are not fully contained, and the availability of a trace element, iodine, whose uptake may be extremely variable depending on the geographical location and the physiological status of individuals. The squaring of the circle has been resolved by the thyroid gland during its phylogenetic maturation by setting up angiofollicular units, morphological entities whose the perfect functional coherence between the different compartments within them (epithelial, endothelial and interstitial) results from a high level three-dimensional assemblage. This morphological and functional integration warrants adequate supplies of thyroid hormones whose mobilization must be triggered at any time when necessary. This functional requirement finds its expression in the morphological heterogeneity that ultimately culminates in the formation of nodules. Each angiofollicular unit is an individualized entity with its own genotypic and phenotypic asset that runs on the extrinsic control of TSH and a host of autocrine and paracrine factors. But subtle intrinsic mechanisms of self-regulation, operating out of any outside influences, constantly adjust the availability of players involved in the hormonal synthesis (iodine, thyroglobulin) within a biochemical entity (the thyroxisome) that is perfectly suited for this synthesis taking place without prejudice to the thyrocyte. The hormonal synthesis generates oxygen-derived substances as oxidative load or stress, though perfectly controlled in healthy thyrocytes. Any injury related to the nature, the amount, or where in the cell oxygen-derived substances are produced, may lead to morphological and functional breakdowns responsible for various disease processes, including those of autoimmune or even neoplastic nature.

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甲状腺血管滤泡单位,功能和形态整合的生物学模型。
甲状腺的基本作用是确保甲状腺激素的生物合成,甲状腺激素在胚胎发育和出生后维持体内平衡的主要作用是众所周知的。这里的挑战是双重的,因为激素的合成既取决于潜在有毒的生化过程,只要它们不被完全控制,又取决于微量元素碘的可用性,碘的摄取可能因地理位置和个人的生理状况而变化很大。在其系统发育成熟过程中,甲状腺通过建立血管滤泡单位解决了圆的平方问题,血管滤泡单位是形态学实体,其内部不同腔室(上皮细胞、内皮细胞和间质细胞)之间的完美功能一致性来自于高水平的三维组合。这种形态和功能的整合保证了甲状腺激素的充足供应,甲状腺激素的动员必须在必要时随时触发。这种功能需求在形态异质性中得到表达,最终导致结节的形成。每个血管滤泡单位都是一个个性化的实体,具有自己的基因型和表型资产,运行在TSH和大量自分泌和旁分泌因素的外在控制下。但微妙的内在自我调节机制,不受任何外界影响,在生化实体(甲状腺酶体)内不断调整参与激素合成(碘,甲状腺球蛋白)的参与者的可用性,这些生化实体非常适合这种合成,而不会损害甲状腺细胞。激素合成产生氧源性物质作为氧化负荷或应激,尽管在健康的甲状腺细胞中完全控制。任何与细胞中产生氧源物质的性质、数量或位置有关的损伤,都可能导致导致各种疾病过程的形态和功能破坏,包括自身免疫甚至肿瘤性质的疾病过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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