School of Medicine, Department of Normal and Pathological Cytology and Histology, University of Seville, Av. Sánchez Pizjuán S/N, 41009, Seville, Andalucía, Spain.
Histochem Cell Biol. 2024 Nov 18;163(1):4. doi: 10.1007/s00418-024-02328-3.
The primary cilium (PC) is a biosensor with diverse functions, depending on cellular type. In the thyroid, where it was first described, PCs are located at the apical pole of the follicular epithelium, sensing the lumen's environment. They probably contribute to follicular homeostasis, although their presence in other thyroid epithelial cells remains unclear. Thyroglobulin, stored in the lumen as colloid, is the primary regulator of thyroid-specific gene expression under constant TSH levels. The mechanism by which thyroglobulin signal is transduced remains unresolved. This study investigates the evolution of PCs in different types of thyroid follicles, based on their functional activity, using both normal human thyroids and functional thyroid pathologies as models. It also compares PC morphology between human and rat thyrocytes and explores their presence in other thyroid epithelial components such as C cells and ultimobranchial remnants. Human and Wistar rat thyroid tissues were analyzed using histological, immunohistochemical, immunofluorescence, and electron microscopy techniques. Morphometric analyses quantified PC changes (frequency and length) in various follicular patterns, and statistical analyses were performed. Four types of thyroid follicles were identified: active, hyperactive, hypoactive, and empty follicles. PCs were most abundant and longest in active and significantly reduced in empty follicles. PCs were more prominent in human than in rat thyrocytes, present in both normal and neoplastic C cells, but sporadic in ultimobranchial remnants. PCs vary according to follicular activity and likely act as mechanosensors in thyroid hormone regulation, detecting colloid density and contributing to the regulation of thyroid hormone biosynthesis.
初级纤毛(PC)是一种具有多种功能的生物传感器,具体功能取决于细胞类型。在甲状腺中,PC 位于滤泡上皮细胞的顶端,感知腔室环境。它们可能有助于滤泡的稳态,尽管它们在其他甲状腺上皮细胞中的存在尚不清楚。甲状腺球蛋白储存在腔室中作为胶体,是在 TSH 水平恒定的情况下调节甲状腺特异性基因表达的主要调节剂。甲状腺球蛋白信号转导的机制仍未解决。本研究使用正常人类甲状腺和功能性甲状腺病理学作为模型,根据其功能活性,研究不同类型甲状腺滤泡中 PC 的进化。它还比较了人类和大鼠甲状腺细胞中 PC 的形态,并探索了它们在 C 细胞和终末鳃裂残余物等其他甲状腺上皮成分中的存在。使用组织学、免疫组织化学、免疫荧光和电子显微镜技术分析人类和 Wistar 大鼠甲状腺组织。形态计量学分析定量了各种滤泡模式中 PC 的变化(频率和长度),并进行了统计分析。确定了四种类型的甲状腺滤泡:活跃滤泡、高活性滤泡、低活性滤泡和空滤泡。PC 在活跃滤泡中最为丰富和最长,在空滤泡中显著减少。PC 在人类甲状腺细胞中比在大鼠甲状腺细胞中更为突出,存在于正常和肿瘤 C 细胞中,但在终末鳃裂残余物中则较为罕见。PC 随滤泡活性而变化,可能作为甲状腺激素调节中的机械感受器,检测胶体密度并有助于甲状腺激素生物合成的调节。