Department of Pharmacology, Vanderbilt University, Nashville, TN, USA; Department of Biochemistry, Vanderbilt University, Nashville, TN, USA.
Department of Biochemistry, Vanderbilt University, Nashville, TN, USA.
Adv Biol Regul. 2022 Jan;83:100858. doi: 10.1016/j.jbior.2021.100858. Epub 2021 Dec 9.
Bisphosphate nucleotidase 2 (BPNT2) is a member of a family of phosphatases that are directly inhibited by lithium, the first-line medication for bipolar disorder. BPNT2 is localized to the Golgi, where it metabolizes the by-products of glycosaminoglycan sulfation reactions. BPNT2-knockout mice exhibit impairments in total-body chondroitin-4-sulfation which lead to abnormal skeletal development (chondrodysplasia). These mice die in the perinatal period, which has previously prevented the investigation of BPNT2 in the adult nervous system. Previous work has demonstrated the importance of chondroitin sulfation in the brain, as chondroitin-4-sulfate is a major component of perineuronal nets (PNNs), a specialized neuronal extracellular matrix which mediates synaptic plasticity and regulates certain behaviors. We hypothesized that the loss of BPNT2 in the nervous system would decrease chondroitin-4-sulfation and PNNs in the brain, which would coincide with behavioral abnormalities. We used Cre-lox breeding to knockout Bpnt2 specifically in the nervous system using Bpnt2 floxed (fl/fl) animals and a Nestin-driven Cre recombinase. These mice are viable into adulthood, and do not display gross physical abnormalities. We identified decreases in total glycosaminoglycan sulfation across selected brain regions, and specifically show decreases in chondroitin-4-sulfation which correspond with increases in chondroitin-6-sulfation. Interestingly, these changes were not correlated with gross alterations in PNNs. We also subjected these mice to a selection of neurobehavioral assessments and did not identify significant behavioral abnormalities. In summary, this work demonstrates that BPNT2, a known target of lithium, is important for glycosaminoglycan sulfation in the brain, suggesting that lithium-mediated inhibition of BPNT2 in the nervous system warrants further investigation.
双磷酸盐核苷酸酶 2(BPNT2)是一类磷酸酶家族的成员,该家族的磷酸酶可被锂直接抑制,锂是治疗双相情感障碍的一线药物。BPNT2 定位于高尔基体,在那里它代谢糖胺聚糖硫酸化反应的副产物。BPNT2 敲除小鼠表现出全身软骨素-4-硫酸化的缺陷,导致骨骼发育异常(软骨发育不良)。这些小鼠在围产期死亡,这以前阻止了对成年神经系统中 BPNT2 的研究。以前的工作表明软骨素硫酸化在大脑中的重要性,因为软骨素-4-硫酸盐是神经周围网络(PNNs)的主要成分,PNNs 是一种特殊的神经元细胞外基质,介导突触可塑性并调节某些行为。我们假设神经系统中 BPNT2 的缺失会降低大脑中的软骨素-4-硫酸化和 PNNs,这与行为异常相一致。我们使用 Cre-lox 繁殖特异性地在神经系统中敲除 Bpnt2,使用 Bpnt2 floxed(fl/fl)动物和 Nestin 驱动的 Cre 重组酶。这些小鼠可存活至成年期,并且没有表现出明显的身体异常。我们确定了选定大脑区域的总糖胺聚糖硫酸化降低,并且特别显示出软骨素-4-硫酸化降低,这与软骨素-6-硫酸化增加相对应。有趣的是,这些变化与 PNNs 的大体改变没有相关性。我们还对这些小鼠进行了一系列神经行为评估,并未发现明显的行为异常。总之,这项工作表明,BPNT2 是锂的已知靶点,对大脑中的糖胺聚糖硫酸化很重要,这表明锂在神经系统中抑制 BPNT2 值得进一步研究。