Summary

突触量化:基于一个免疫细胞化学检测,以量化突触数量

Published: November 16, 2010
doi:

Summary

该协议的细节,如何量化,在分离神经元的文化和突触数量在脑切片,用免疫细胞化学。使用车厢的特异性抗体,我们的标签突触前终端以及突触后专业化的网站。我们定义这些标记所产生的信号的共定位点之间的突触。

Abstract

在神经科学中最重要的目标之一是要了解分子线索指示突触形成的早期阶段。因此,它已成为当务之急,制定客观的方法来量化突触连接的变化。从样品固定开始,这个协议的细节如何量化无论是在分离的神经元文化和在脑切片,用免疫细胞化学突触的数量。使用车厢的特异性抗体,我们的标签突触前终端以及突触后专业化的网站。我们定义这些标记所产生的信号的共定位点之间的突触。这些colocalizations量化Puncta分析器(巴里Wark,可根据要求,c.eroglu @ cellbio.duke.edu书面)使用ImageJ分析软件平台下的一个插件。在本议定书中所描述的突触检测可应用于任何神经组织或文化的准备,你有选择性的前和突触后标记。这突触法是一种宝贵的的工具,可以被广泛利用在突触发展的研究。

Protocol

准备的解决方案: 抗体缓冲液: 150 mM氯化钠 50 mM的三基(费舍尔​​,猫编号:BP152 – 5,50毫米) – 1.21克 1%BSA(Sigma公司,没有猫:A2153,1%) – 2.0克 100毫米L -赖氨酸(西格玛,猫编号:L – 1137,100毫米) – 3.65克调整pH值至7.4 0.04%叠氮音量调整到200毫升,用蒸馏水H 2 O 通过0.22μm的过滤器的过滤器(Millipore公司,卡?…

Discussion

上文所述突触检测是基于在我们的实验目标,其中主要集中于视网膜神经节细胞兴奋的预测中,无论是在纯化的文化,或在大脑部分。我们提供了一个参考表中列出的标签(见表1)兴奋性突触的抗体,工作。

这种突触的检测,可适应量化任何神经元的人口或任何其他的突触亚型,这是有选择性的前和突触后标记的突触数量。例如,突触实验描述在这里可以应用到研究的GABA – …

Offenlegungen

The authors have nothing to disclose.

Acknowledgements

Puncta分析仪插入图像J的巴里Wark(地址:Physion咨询)写在本A.巴雷斯实验室(斯坦福大学)。

资金;

  • Alfred P. Sloan基金会
  • 以斯帖A.和约瑟夫Klingenstein基金公司
  • 广泛的生物医学研究基金会
  • 治疗亨廷顿氏病倡议

Materials

  Antigen Species Monoclonal/Polyclonal Vendor Catalog Number Dilution Works in Culture Works in Sections
Presynaptic Synapsin Rabbit Polyclonal Synaptic Systems 106004 1:750 Y N.D.
Synapsin Mouse Monoclonal Synaptic Systems 106001 1:500 Y Y
Bassoon Mouse Monoclonal Assay Designs VAM-PS003F 1:500 Y Y
Bassoon Guinea Pig Polyclonal Synaptic Systems 141004 1:1000 Y N.D.
Synaptotagmin 1 Rabbit Polyclonal Synaptic Systems 105002 1:750 Y N
Synaptobrevin 2
(C1.69.1)
Mouse Monoclonal Synaptic Systems 104211 1:500 Y Y
Synaptophysin
(C1.7.2)
Mouse Monoclonal Synaptic Systems 101011 1:500 Y Y
VGlut1 Mouse Monoclonal Millipore MAB5502 1:2500 N Y
VGlut1 Guinea pig Polyclonal Millipore AB5905 1:2500 N Y
VGlut2 Guinea pig Polyclonal Millipore AB2251 1:2500 N Y
Postsynaptic PSD-95
(6G6-1C9 clone)
Mouse Monoclonal Affinity Bio Reagents MA1-045 1:750 Y N
PSD-95 Rabbit Polyclonal Zymed 51-6900 1:500 N Y
Homer Mouse Monoclonal Synaptic Systems 160011 1:500 Y N.D.
Homer Rat Polyclonal Millipore AB5875 1:500 Y Y
Gephyrin Rabbit Polyclonal Synaptic Systems 147003 1:500 Y Y
Gephyrin Mouse Monoclonal Synaptic Systems 147 1:200 Y Y

Table 1: Lists examples of good pre- and postsynaptic markers that we have successfully utilized in our synapse assay. Be aware that this is not an exhaustive list of all available markers. Y = Yes, N = No, N.D. = Not Determined.

Reagent Company Cat. No.
PBS Invitrogen 20012-027
poly-d-lysine Sigma P6407
Laminin Cultrex 3400-010-01
Triton X-100 Roche Diagnostics Gmbh 9002-93-1
Normal Goat Serum Gibco 16210
VectaShield with DAPI Vector Laboratories H-1200
OCT Tissue-Tek 4583
Tris-Base (50 mM) Fisher BP152-5
Bovine Serum Albumin Sigma A2153
l-lysine Sigma L-1137
16% PFA solution Electron Microscopy Sciences 15711
Granular PFA Electron Microscopy Sciences 19210
24-well culture plate Falcon 35-3047
Goat anti-mouse Alexa conjugated antibodies Invitrogen
Supply Company Cat. No.
12mm, No. 0 glass coverslips Karl Hecht Gmbh 1105209
No. 1.5 glass coverslip (for slices) VWR Scientific 48393241
Glass slides VWR Scientific 48311-703

Referenzen

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Diesen Artikel zitieren
Ippolito, D. M., Eroglu, C. Quantifying Synapses: an Immunocytochemistry-based Assay to Quantify Synapse Number. J. Vis. Exp. (45), e2270, doi:10.3791/2270 (2010).

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