Centro de Genética y Genómica, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago 7590943, Chile.
Departamento de Gastroenterología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Int J Mol Sci. 2018 Nov 14;19(11):3599. doi: 10.3390/ijms19113599.
Niemann⁻Pick type C (NPC) disease is a rare neurovisceral cholesterol storage disorder that arises from loss of function mutations in the or genes. Soon after birth, some patients present with an aggressive hepatosplenomegaly and cholestatic signs. Histopathologically, the liver presents with large numbers of foam cells; however, their role in disease pathogenesis has not been explored in depth. Here, we studied the consequences of gadolinium chloride (GdCl₃) treatment, a well-known Kupffer/foam cell inhibitor, at late stages of NPC liver disease and compared it with NPC1 genetic rescue in hepatocytes in vivo. GdCl₃ treatment successfully blocked the endocytic capacity of hepatic Kupffer/foam measured by India ink endocytosis, decreased the levels CD68-A marker of Kupffer cells in the liver-and normalized the transaminase levels in serum of NPC mice to a similar extent to those obtained by genetic rescue of liver cells. Gadolinium salts are widely used as magnetic resonance imaging (MRI) contrasts. This study opens the possibility of targeting foam cells with gadolinium or by other means for improving NPC liver disease. Synopsis: Gadolinium chloride can effectively rescue some parameters of liver dysfunction in NPC mice and its potential use in patients should be carefully evaluated.
尼曼-皮克 C 型(NPC)病是一种罕见的神经内脏胆固醇贮积症,由 或 基因功能丧失突变引起。一些患者在出生后不久就表现出侵袭性肝脾肿大和胆汁淤积的迹象。组织病理学上,肝脏有大量泡沫细胞;然而,其在疾病发病机制中的作用尚未深入探讨。在这里,我们研究了氯化钆(GdCl₃)治疗的后果,氯化钆是一种众所周知的枯否细胞/泡沫细胞抑制剂,在 NPC 肝病的晚期,并将其与体内肝细胞中 NPC1 基因挽救进行了比较。GdCl₃ 治疗成功地阻断了印度墨汁内吞作用测量的肝枯否/泡沫细胞的内吞能力,降低了肝中 CD68-A 标记物枯否细胞的水平,并使 NPC 小鼠血清中转氨酶水平正常化到与通过肝细胞遗传挽救获得的相似程度。钆盐被广泛用作磁共振成像(MRI)造影剂。这项研究为用钆或其他方法靶向泡沫细胞以改善 NPC 肝病开辟了可能性。概要:氯化钆可有效挽救 NPC 小鼠一些肝功能障碍的参数,其在患者中的潜在应用应仔细评估。