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首页> 外文期刊>Journal of Neuropathology and Experimental Neurology >Leucine-Rich Repeat Kinase 2 Is Associated With the Endoplasmic Reticulum in Dopaminergic Neurons and Accumulates in the Core of Lewy Bodies in Parkinson Disease
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Leucine-Rich Repeat Kinase 2 Is Associated With the Endoplasmic Reticulum in Dopaminergic Neurons and Accumulates in the Core of Lewy Bodies in Parkinson Disease

机译:富含亮氨酸的重复激酶2与多巴胺能神经元的内质网相关,并在帕金森氏病的路易体的核心中积累。

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Mutation of the leucine-rich repeat kinase 2 (LRRK2) gene is the most frequent genetic cause of Parkinson disease (PD). To understand the role of LRRK2 in the neuropathology of PD, we investigated the protein expression in a healthy brain and brains from patients with PD and its subcellular localization in dopaminergic neurons. LRRK2 was found to be widely expressed in healthy adult brain, including areas involved in PD. By double fluorescent staining, we found that endogenous LRRK2 is colocalized with the endoplasmic reticulum (ER) markers Neurotrace and KDEL in human dopaminergic neurons. Labeling of brain sections with anti-LRRK2 and anti-α-synuclein antibodies revealed localization of LRRK2 in the core of 24% of Lewy bodies (LBs) in the substantia nigra and 11% of LBs in the locus coeruleus in idiopathic PD patients. The percentage was increased to 50% in both areas in a patient with the G2019S LRRK2 mutation. The finding of ER localization suggests the possibility that LRRK2 is involved in the ER stress response and could account for the susceptibility to neuronal degeneration of LRRK2 mutation carriers. The localization of LRRK2 protein in the core of a subset of LBs demonstrates the contribution of LRRK2 to LB formation and disease pathogenesis.
机译:富含亮氨酸的重复激酶2(LRRK2)基因的突变是帕金森病(PD)的最常见遗传原因。为了了解LRRK2在PD神经病理学中的作用,我们研究了PD患者在健康大脑和大脑中的蛋白表达及其在多巴胺能神经元中的亚细胞定位。 LRRK2被发现在健康的成人大脑中广泛表达,包括参与PD的区域。通过双荧光染色,我们发现内源性LRRK2与人多巴胺能神经元中的内质网(ER)标记Neurotrace和KDEL共定位。用抗LRRK2和抗α-突触核蛋白抗体标记脑切片显示,特发性PD患者中LRRK2定位于黑质中路易体(LB)的核心的24%,蓝斑中的LB的11%。患有G2019S LRRK2突变的患者的两个区域的百分比均增加到50%。内质网定位的发现提示LRRK2参与内质网应激反应的可能性,并可能解释了LRRK2突变携带者对神经元变性的易感性。 LRRK2蛋白在LB子集的核心中的定位表明LRRK2对LB形成和疾病发病机制的贡献。

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    Jérémic Vitte, PhD, Sabine Traver, PhD, André Maués De Paula, MD, Suzanne Lesage, PhD, Giorgio Rovelli, PhD, Olga Corti, PhD, Charles Duyckaerts, MD, PhD, and Alexis Brice, MDFrom the Laboratory of Molecular Basis, Physiopathology and Treatment of Neurodegenerative Diseases (JV, ST, SL, OC, CD, AB), Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Paris, France, INSERM U975 (JV, ST, SL, OC, CD, AB), Paris, France, CNRS UMR 7225 (JV, ST, SL, OC, CD, AB), Paris, France, Service d'Anatomie Pathologique et de Neuropathologie (AMDP), CHU Timone, Marseille, France, Novartis Institute for BioMedical Research (GR), Basel, Switzerland, Alzheimer Disease Prion disease Team (CD), Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Paris, France, Laboratoire de Neuropathologie Raymond Escourolle (CD), Pierre and Marie Curie-Paris 6 University, Paris, France, and AP-HP, Assistance Publique Hôpitaux de Paris (AB), Groupe Hospitalier Pitié-Salpêtrière, Paris, France.Send correspondence and reprint requests to: Alexis Brice, MD, INSERM UMR S975, Centre de Recherche Institut du Cerveau et de la Moelle, Groupe Hospitalier Pitié Salpêtrière, 47 Bd de l'Hôpital, 75 651 Paris Cedex 13, France, E-mail: alexis.brice@upmc.frThis research was supported by the Institut National de la Santé et de la Recherche Médicale and Agence Nationale de la Recherche (ANR-05-NEUR-019-01/A05169DS).Online-only figures are available at http://www.jneuropath.com.,;

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