Mollá Belén, Riveiro Fátima, Bolinches-Amorós Arantxa, Muñoz-Lasso Diana C, Palau Francesc, González-Cabo Pilar
Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit at CIPF, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain CIBER de Enfermedades Raras (CIBERER), Valencia 28029, Spain.
Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit at CIPF, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain Cell Therapy Program, Centro de Investigación Príncipe Felipe (CIPF), Valencia 46012, Spain.
Dis Model Mech. 2016 Jun 1;9(6):647-57. doi: 10.1242/dmm.024273. Epub 2016 Apr 14.
Frataxin (FXN) deficiency causes Friedreich's ataxia (FRDA), a multisystem disorder with neurological and non-neurological symptoms. FRDA pathophysiology combines developmental and degenerative processes of dorsal root ganglia (DRG), sensory nerves, dorsal columns and other central nervous structures. A dying-back mechanism has been proposed to explain the peripheral neuropathy and neuropathology. In addition, affected individuals have non-neuronal symptoms such as diabetes mellitus or glucose intolerance. To go further in the understanding of the pathogenic mechanisms of neuropathy and diabetes associated with the disease, we have investigated the humanized mouse YG8R model of FRDA. By biochemical and histopathological studies, we observed abnormal changes involving muscle spindles, dorsal root axons and DRG neurons, but normal findings in the posterior columns and brain, which agree with the existence of a dying-back process similar to that described in individuals with FRDA. In YG8R mice, we observed a large number of degenerated axons surrounded by a sheath exhibiting enlarged adaxonal compartments or by a thin disrupted myelin sheath. Thus, both axonal damage and defects in Schwann cells might underlie the nerve pathology. In the pancreas, we found a high proportion of senescent islets of Langerhans in YG8R mice, which decreases the β-cell number and islet mass to pathological levels, being unable to maintain normoglycemia. As a whole, these results confirm that the lack of FXN induces different pathogenic mechanisms in the nervous system and pancreas in the mouse model of FRDA: dying back of the sensory nerves, and pancreatic senescence.
弗里德赖希共济失调(FRDA)由铁调素(FXN)缺乏引起,是一种具有神经和非神经症状的多系统疾病。FRDA的病理生理学结合了背根神经节(DRG)、感觉神经、后索和其他中枢神经结构的发育和退化过程。有人提出一种逆行性变性机制来解释周围神经病变和神经病理学。此外,受影响个体还有非神经元症状,如糖尿病或葡萄糖不耐受。为了进一步了解与该疾病相关的神经病变和糖尿病的致病机制,我们研究了FRDA的人源化小鼠YG8R模型。通过生化和组织病理学研究,我们观察到涉及肌梭、背根轴突和DRG神经元的异常变化,但后索和大脑未见异常,这与FRDA患者中描述的逆行性变性过程一致。在YG8R小鼠中,我们观察到大量退化的轴突被具有扩大的轴突旁间隙的鞘或薄的、破坏的髓鞘包围。因此,轴突损伤和施万细胞缺陷可能是神经病理学的基础。在胰腺中,我们发现YG8R小鼠中有高比例的衰老胰岛,这将β细胞数量和胰岛质量降低到病理水平,无法维持正常血糖水平。总体而言,这些结果证实,在FRDA小鼠模型中,FXN的缺乏在神经系统和胰腺中诱导了不同的致病机制:感觉神经的逆行性变性和胰腺衰老。