Wang Da-Yong, Wang Yang
Key Laboratory of Developmental Genes and Human Disease in Ministry of Education, Department of Genetics and Developmental Biology, Southeast University Medical school, Nanjing 210009, China.
Neurosci Bull. 2009 Apr;25(2):75-86. doi: 10.1007/s12264-009-0119-9.
To study the role of HLB-1 in regulating the organization and function of neuromuscular junctions in nematode Caenorhabditis elegans.
To evaluate the functions of HLB-1 in regulating the organization and function of neuromuscular junctions, effects of hlb-1 mutation on the synaptic structures were revealed by uncovering the expression patterns of SNB-1::GFP and UNC-49::GFP, and pharmacologic assays with aldicarb and levamisole were also used to test the synaptic functions. Further rescue and mosaic analysis confirmed HLB-1's role in regulating the organization and function of neuromuscular junctions.
Loss of HLB-1 function did not result in defects in neuronal outgrowth or neuronal loss, but caused obvious defects of SNB-1::GFP and UNC-49::GFP puncta localization, suggesting the altered presynaptic and postsynaptic structures. The mutant animals exhibited severe defects in locomotion behaviors and altered responses to an inhibitor of acetylcholinesterase and a cholinergic agonist, indicating the altered presynaptic and postsynaptic functions. Rescue and mosaic analysis experiments suggested that HLB-1 regulated synaptic functions in a cell nonautonomously way. Moreover, HLB-1 expression was not required for the presynaptic active zone morphology. Genetic evidence further demonstrated that hlb-1 acted in a parallel pathway with syd-2 to regulate the synaptic functions.
HLB-1 appeared as a new regulator for the organization and function of neuromuscular junctions in C. elegans.
研究HLB-1在调控线虫秀丽隐杆线虫神经肌肉接头的组织和功能中的作用。
为评估HLB-1在调控神经肌肉接头组织和功能方面的作用,通过揭示SNB-1::GFP和UNC-49::GFP的表达模式来揭示hlb-1突变对突触结构的影响,并且还使用涕灭威和左旋咪唑进行药理学分析来测试突触功能。进一步的拯救和嵌合体分析证实了HLB-1在调控神经肌肉接头组织和功能中的作用。
HLB-1功能丧失并未导致神经元生长缺陷或神经元丢失,但导致SNB-1::GFP和UNC-49::GFP斑点定位出现明显缺陷,表明突触前和突触后结构发生改变。突变动物在运动行为上表现出严重缺陷,并且对乙酰胆碱酯酶抑制剂和胆碱能激动剂的反应发生改变,表明突触前和突触后功能发生改变。拯救和嵌合体分析实验表明,HLB-1以非细胞自主方式调节突触功能。此外,突触前活性区形态不需要HLB-1表达。遗传学证据进一步证明,hlb-1与syd-2在平行途径中发挥作用以调节突触功能。
HLB-1似乎是秀丽隐杆线虫神经肌肉接头组织和功能的新调节因子。