Hall Małgorzata H, Magalska Adriana, Malinowska Monika, Ruszczycki Błażej, Czaban Iwona, Patel Satyam, Ambrożek-Latecka Magdalena, Zołocińska Ewa, Broszkiewicz Hanna, Parobczak Kamil, Nair Rajeevkumar R, Rylski Marcin, Pawlak Robert, Bramham Clive R, Wilczyński Grzegorz M
Laboratory of Molecular and Systemic Neuromorphology, Department of Neurophysiology, Nencki Institute of Experimental Biology, Pasteura 3, 02-093, Warsaw, Poland.
Department of Cell Physiology and Pharmacology, University of Leicester, University Road, Leicester, LE1 7RH, UK.
Brain Struct Funct. 2016 Jun;221(5):2511-25. doi: 10.1007/s00429-015-1053-4. Epub 2015 May 9.
PML is a tumor suppressor protein involved in the pathogenesis of promyelocytic leukemia. In non-neuronal cells, PML is a principal component of characteristic nuclear bodies. In the brain, PML has been implicated in the control of embryonic neurogenesis, and in certain physiological and pathological phenomena in the adult brain. Yet, the cellular and subcellular localization of the PML protein in the brain, including its presence in the nuclear bodies, has not been investigated comprehensively. Because the formation of PML bodies appears to be a key aspect in the function of the PML protein, we investigated the presence of these structures and their anatomical distribution, throughout the adult mouse brain. We found that PML is broadly expressed across the gray matter, with the highest levels in the cerebral and cerebellar cortices. In the cerebral cortex PML is present exclusively in neurons, in which it forms well-defined nuclear inclusions containing SUMO-1, SUMO 2/3, but not Daxx. At the ultrastructural level, the appearance of neuronal PML bodies differs from the classic one, i.e., the solitary structure with more or less distinctive capsule. Rather, neuronal PML bodies have the form of small PML protein aggregates located in the close vicinity of chromatin threads. The number, size, and signal intensity of neuronal PML bodies are dynamically influenced by immobilization stress and seizures. Our study indicates that PML bodies are broadly involved in activity-dependent nuclear phenomena in adult neurons.
早幼粒细胞白血病蛋白(PML)是一种参与早幼粒细胞白血病发病机制的肿瘤抑制蛋白。在非神经细胞中,PML是特征性核小体的主要成分。在大脑中,PML与胚胎神经发生的调控以及成人大脑的某些生理和病理现象有关。然而,PML蛋白在大脑中的细胞和亚细胞定位,包括其在核小体中的存在情况,尚未得到全面研究。由于PML小体的形成似乎是PML蛋白功能的一个关键方面,我们研究了这些结构在成年小鼠全脑的存在情况及其解剖分布。我们发现PML在灰质中广泛表达,在大脑皮质和小脑皮质中表达水平最高。在大脑皮质中,PML仅存在于神经元中,在神经元中它形成明确的核内包涵体,其中含有小泛素样修饰物1(SUMO-1)、小泛素样修饰物2/3(SUMO 2/3),但不含有死亡结构域相关蛋白(Daxx)。在超微结构水平上,神经元PML小体的外观与经典的不同,即具有或多或少独特包膜的孤立结构。相反,神经元PML小体呈小PML蛋白聚集体的形式,位于染色质丝附近。神经元PML小体的数量、大小和信号强度受到固定应激和癫痫发作的动态影响。我们的研究表明,PML小体广泛参与成年神经元中与活动相关的核现象。