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胶质细胞在 Ube3a 依赖性 ASD 中神经元棘突形成失调中的作用。

The role of glia in the dysregulation of neuronal spinogenesis in Ube3a-dependent ASD.

机构信息

Department of Biology, Boston University, 5 Cummington Mall, Boston, MA 02215, United States of America.

Department of Biology, Boston University, 5 Cummington Mall, Boston, MA 02215, United States of America; Department of Pharmacology, Physiology & Biophysics, Boston University School of Medicine, 72 East Concord St., L-603, Boston, MA 02118, United States of America; Center for Systems Neuroscience, Boston University, 610 Commonwealth Ave, Boston, MA 02215, United States of America.

出版信息

Exp Neurol. 2024 Jun;376:114756. doi: 10.1016/j.expneurol.2024.114756. Epub 2024 Mar 18.

Abstract

Overexpression of the Ube3a gene and the resulting increase in Ube3a protein are linked to autism spectrum disorder (ASD). However, the cellular and molecular processes underlying Ube3a-dependent ASD remain unclear. Using both male and female mice, we find that neurons in the somatosensory cortex of the Ube3a 2× Tg ASD mouse model display reduced dendritic spine density and increased immature filopodia density. Importantly, the increased gene dosage of Ube3a in astrocytes alone is sufficient to confer alterations in neurons as immature dendritic protrusions, as observed in primary hippocampal neuron cultures. We show that Ube3a overexpression in astrocytes leads to a loss of astrocyte-derived spinogenic protein, thrombospondin-2 (TSP2), due to a suppression of TSP2 gene transcription. By neonatal intraventricular injection of astrocyte-specific virus, we demonstrate that Ube3a overexpression in astrocytes in vivo results in a reduction in dendritic spine maturation in prelimbic cortical neurons, accompanied with autistic-like behaviors in mice. These findings reveal an astrocytic dominance in initiating ASD pathobiology at the neuronal and behavior levels. SIGNIFICANCE STATEMENT: Increased gene dosage of Ube3a is tied to autism spectrum disorders (ASDs), yet cellular and molecular alterations underlying autistic phenotypes remain unclear. We show that Ube3a overexpression leads to impaired dendritic spine maturation, resulting in reduced spine density and increased filopodia density. We find that dysregulation of spine development is not neuron autonomous, rather, it is mediated by an astrocytic mechanism. Increased gene dosage of Ube3a in astrocytes leads to reduced production of the spinogenic glycoprotein thrombospondin-2 (TSP2), leading to abnormalities in spines. Astrocyte-specific Ube3a overexpression in the brain in vivo confers dysregulated spine maturation concomitant with autistic-like behaviors in mice. These findings indicate the importance of astrocytes in aberrant neurodevelopment and brain function in Ube3a-depdendent ASD.

摘要

Ube3a 基因的过度表达及其导致的 Ube3a 蛋白增加与自闭症谱系障碍(ASD)有关。然而,Ube3a 依赖性 ASD 背后的细胞和分子过程仍不清楚。使用雄性和雌性小鼠,我们发现 Ube3a 2×Tg ASD 小鼠模型的体感皮层神经元显示出树突棘密度降低和不成熟丝状伪足密度增加。重要的是,仅在星形胶质细胞中增加 Ube3a 的基因剂量足以赋予神经元作为不成熟树突状突起的改变,正如在原代海马神经元培养物中观察到的那样。我们表明,星形胶质细胞中的 Ube3a 过表达导致星形胶质细胞衍生的 spinogenic 蛋白,即血小板反应蛋白 2(TSP2)的丧失,这是由于 TSP2 基因转录的抑制。通过新生鼠脑室注射星形胶质细胞特异性病毒,我们证明体内星形胶质细胞中的 Ube3a 过表达导致额前皮质神经元树突棘成熟减少,同时伴有小鼠的自闭症样行为。这些发现揭示了星形胶质细胞在神经元和行为水平上引发 ASD 病理生物学的优势。

意义

Ube3a 基因剂量增加与自闭症谱系障碍(ASD)有关,但自闭症表型背后的细胞和分子改变仍不清楚。我们表明,Ube3a 过表达导致树突棘成熟受损,导致树突棘密度降低和丝状伪足密度增加。我们发现,棘突发育的失调不是神经元自主的,而是由星形胶质细胞机制介导的。星形胶质细胞中 Ube3a 基因剂量的增加导致产生棘突生成糖蛋白血小板反应蛋白 2(TSP2)减少,导致棘突异常。体内大脑中星形胶质细胞特异性 Ube3a 过表达赋予异常的棘突成熟,同时伴有小鼠的自闭症样行为。这些发现表明,星形胶质细胞在 Ube3a 依赖性 ASD 中异常的神经发育和大脑功能中具有重要意义。

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