Kement Dilara, Reumann Rebecca, Schostak Katrin, Voß Hannah, Douceau Sara, Dottermusch Matthias, Schweizer Michaela, Schlüter Hartmut, Vivien Denis, Glatzel Markus, Galliciotti Giovanna
Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Institute of Clinical Chemistry and Laboratory Medicine, Mass Spectrometric Proteomics Group, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Front Neuroanat. 2021 Feb 23;15:627896. doi: 10.3389/fnana.2021.627896. eCollection 2021.
Neuroserpin is a serine protease inhibitor that regulates the activity of tissue-type plasminogen activator (tPA) in the nervous system. Neuroserpin is strongly expressed during nervous system development as well as during adulthood, when it is predominantly found in regions eliciting synaptic plasticity. In the hippocampus, neuroserpin regulates developmental neurogenesis, synaptic maturation and in adult mice it modulates synaptic plasticity and controls cognitive and social behavior. High expression levels of neuroserpin in the neocortex starting from prenatal stage and persisting during adulthood suggest an important role for the serpin in the formation of this brain region and in the maintenance of cortical functions. In order to uncover neuroserpin function in the murine neocortex, in this work we performed a comprehensive investigation of its expression pattern during development and in the adulthood. Moreover, we assessed the role of neuroserpin in cortex formation by comparing cortical lamination and neuronal maturation between neuroserpin-deficient and control mice. Finally, we evaluated a possible regulatory role of neuroserpin at cortical synapses in neuroserpin-deficient mice. We observed that neuroserpin is expressed starting from the beginning of corticogenesis until adulthood throughout the neocortex in several classes of glutamatergic projection neurons and GABA-ergic interneurons. However, in the absence of neuroserpin we did not detect any alteration either in cortical layer formation, or in neuronal soma size and dendritic length. Furthermore, no significant quantitative changes were observed in the proteome of cortical synapses upon neuroserpin deficiency. We conclude that, although strongly expressed in the neocortex, absence of neuroserpin does not lead to gross developmental abnormalities, and does not perturb the composition of the cortical synaptic proteome.
神经丝氨酸蛋白酶抑制剂是一种丝氨酸蛋白酶抑制剂,可调节神经系统中组织型纤溶酶原激活剂(tPA)的活性。神经丝氨酸蛋白酶抑制剂在神经系统发育期间以及成年期均强烈表达,成年期时主要存在于引发突触可塑性的区域。在海马体中,神经丝氨酸蛋白酶抑制剂调节发育性神经发生、突触成熟,在成年小鼠中,它调节突触可塑性并控制认知和社交行为。从产前阶段开始并持续到成年期,新皮质中神经丝氨酸蛋白酶抑制剂的高表达水平表明该丝氨酸蛋白酶抑制剂在这个脑区的形成以及皮质功能的维持中发挥重要作用。为了揭示神经丝氨酸蛋白酶抑制剂在小鼠新皮质中的功能,在这项研究中,我们对其在发育过程和成年期的表达模式进行了全面研究。此外,我们通过比较神经丝氨酸蛋白酶抑制剂缺陷小鼠和对照小鼠的皮质分层和神经元成熟情况,评估了神经丝氨酸蛋白酶抑制剂在皮质形成中的作用。最后,我们评估了神经丝氨酸蛋白酶抑制剂在神经丝氨酸蛋白酶抑制剂缺陷小鼠皮质突触处可能的调节作用。我们观察到,从皮质发生开始到成年期,神经丝氨酸蛋白酶抑制剂在新皮质的几类谷氨酸能投射神经元和γ-氨基丁酸能中间神经元中均有表达。然而,在缺乏神经丝氨酸蛋白酶抑制剂的情况下,我们未检测到皮质层形成、神经元胞体大小或树突长度有任何改变。此外,神经丝氨酸蛋白酶抑制剂缺乏时,皮质突触蛋白质组未观察到明显的定量变化。我们得出结论,尽管神经丝氨酸蛋白酶抑制剂在新皮质中强烈表达,但缺乏该蛋白不会导致明显的发育异常,也不会扰乱皮质突触蛋白质组的组成。