Generation and Characterization of Specific Monoclonal Antibodies and Nanobodies Directed Against the ATP-Gated Channel P2X4

被引:11
|
作者
Bergmann, Philine [1 ]
de Paco, Elvira Garcia [2 ,3 ]
Rissiek, Bjoern [4 ]
Menzel, Stephan [1 ]
Dubberke, Gudrun [1 ]
Hua, Jennifer [2 ,3 ]
Rassendren, Francois [2 ,3 ]
Ulmann, Lauriane [2 ,3 ]
Koch-Nolte, Friedrich [1 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Inst Immunol, Hamburg, Germany
[2] Univ Montpellier, CNRS, INSERM, IGF, Montpellier, France
[3] Lab Excellence Canaux Ion Interet Therapeut LabEx, Montpellier, France
[4] Univ Med Ctr Hamburg Eppendorf, Dept Neurol, Hamburg, Germany
关键词
purinergic receptors; monoclonal antibody; nanobody; immunoprecipitation; cytometry; P2X(4) RECEPTORS; SPINAL MICROGLIA; EXPRESSION; RELEASE;
D O I
10.3389/fncel.2019.00498
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The P2X4 channel is involved in different physiological and pathological conditions and functions in the nervous system. Despite the existence of several mouse models for which the expression of the gene was manipulated, there is still little information on the expression of the protein at the cellular level. In particular, supposedly specific available antibodies have often proved to recognize unrelated proteins in P2X4-deficient mice. Here, we used an in vivo DNA vaccine approach to generate a series of monoclonal antibodies and nanobodies specific for human, mouse, and rat P2X4 channels. We further characterized these antibodies and show that they solely recognize the native form of the proteins both in biochemical and cytometric applications. Some of these antibodies prove to specifically recognize P2X4 channels by immunostaining in brain or sensory ganglia slices, as well as at the cellular and subcellular levels. Due to their clonality, these different antibodies should represent versatile tools for further characterizing the cellular functions of P2X4 in the nervous system as well as at the periphery.
引用
收藏
页数:12
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