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Signaling pathways involved in vascular smooth muscle cell calcification during hyperphosphatemia

机译:高磷血症期间参与血管平滑肌细胞钙化的信号通路

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摘要

Medial vascular calcification has emerged as a putative key factor contributing to the excessive cardiovascular mortality of patients with chronic kidney disease (CKD). Hyperphosphatemia is considered a decisive determinant of vascular calcification in CKD. A critical role in initiation and progression of vascular calcification during elevated phosphate conditions is attributed to vascular smooth muscle cells (VSMCs), which are able to change their phenotype into osteo-/chondroblasts-like cells. These transdifferentiated VSMCs actively promote calcification in the medial layer of the arteries by producing a local pro-calcifying environment as well as nidus sites for precipitation of calcium and phosphate and growth of calcium phosphate crystals. Elevated extracellular phosphate induces osteo-/chondrogenic transdifferentiation of VSMCs through complex intracellular signaling pathways, which are still incompletely understood. The present review addresses critical intracellular pathways controlling osteo-/chondrogenic transdifferentiation of VSMCs and, thus, vascular calcification during hyperphosphatemia. Elucidating these pathways holds a significant promise to open novel therapeutic opportunities counteracting the progression of vascular calcification in CKD.
机译:内侧血管钙化已成为慢性肾脏病(CKD)患者过度心血管死亡的推定关键因素。高磷血症被认为是CKD中血管钙化的决定性决定因素。在磷酸盐升高的条件下,血管钙化的开始和进展中的关键作用归因于血管平滑肌细胞(VSMC),该细胞能够将其表型改变为成骨/成软骨细胞样细胞。这些转分化的VSMC通过产生局部前钙化环境以及钙盐和磷酸盐沉淀以及磷酸钙晶体生长的病菌部位,积极地促进动脉内侧钙化。升高的细胞外磷酸通过复杂的细胞内信号传导途径诱导VSMC的骨/软骨转分化,目前尚不完全清楚。本文综述了控制血管平滑肌细胞的骨/软骨转分化的关键细胞内途径,从而控制了高磷酸盐血症期间的血管钙化。阐明这些途径具有打开消除CKD中血管钙化进展的新治疗机会的重大希望。

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