A Cre-dependent reporter mouse for quantitative real-time imaging of protein kinase A activity dynamics

被引:2
作者
Tilden, Elizabeth I. [1 ,2 ]
Maduskar, Aditi [1 ]
Oldenborg, Anna [1 ]
Sabatini, Bernardo L. [3 ]
Chen, Yao [1 ]
机构
[1] Washington Univ, Dept Neurosci, St Louis, MO 63130 USA
[2] Washington Univ, Ph D Program Neurosci, St Louis, MO USA
[3] Harvard Med Sch, Howard Hughes Med Inst, Dept Neurobiol, Boston, MA USA
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
NERVE GROWTH-FACTOR; PC12; CELLS; SUBCELLULAR DYNAMICS; MAP KINASE; EXPRESSION; DOPAMINE; PKA; RECOMBINASE; DISRUPTION; MODULATION;
D O I
10.1038/s41598-024-53313-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intracellular signaling dynamics play a crucial role in cell function. Protein kinase A (PKA) is a key signaling molecule that has diverse functions, from regulating metabolism and brain activity to guiding development and cancer progression. We previously developed an optical reporter, FLIM-AKAR, that allows for quantitative imaging of PKA activity via fluorescence lifetime imaging microscopy and photometry. However, using viral infection or electroporation for the delivery of FLIM-AKAR is invasive and results in variable expression. Here, we developed a reporter mouse, FL-AK, which expresses FLIM-AKAR in a Cre-dependent manner from the ROSA26 locus. FL-AK provides robust and consistent expression of FLIM-AKAR over time. Functionally, the mouse line reports an increase in PKA activity in response to activation of both G(alpha s) and G(alpha q)-coupled receptors in brain slices. In vivo, FL-AK reports PKA phosphorylation in response to neuromodulator receptor activation. Thus, FL-AK provides a quantitative, robust, and flexible method to reveal the dynamics of PKA activity in diverse cell types.
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页数:11
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