Synthetic Biology Meets Ca2+ Release-Activated Ca2+ Channel-Dependent Immunomodulation

被引:1
|
作者
Bacsa, Bernadett [1 ]
Hopl, Valentina [2 ]
Derler, Isabella [2 ]
机构
[1] Med Univ Graz, Div Med Phys & Biophys, A-8010 Graz, Austria
[2] Johannes Kepler Univ Linz, Inst Biophys, JKU Life Sci Ctr, A-4020 Linz, Austria
基金
奥地利科学基金会;
关键词
CRAC channels; STIM1; Orai1; calcium (Ca2+) synthetic biology; chemical inducers of dimerization; proteolytic cleavage; optogenetics; engineered immune cells; STROMAL INTERACTION MOLECULE-1; TUBULAR AGGREGATE MYOPATHY; CALCIUM SENSOR STIM1; CLICK AMINO-ACIDS; NF-KAPPA-B; T-CELLS; CRAC CHANNELS; ORAI PROTEINS; SIGNAL-TRANSDUCTION; CROSS-LINKING;
D O I
10.3390/cells13060468
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many essential biological processes are triggered by the proximity of molecules. Meanwhile, diverse approaches in synthetic biology, such as new biological parts or engineered cells, have opened up avenues to precisely control the proximity of molecules and eventually downstream signaling processes. This also applies to a main Ca2+ entry pathway into the cell, the so-called Ca2+ release-activated Ca2+ (CRAC) channel. CRAC channels are among other channels are essential in the immune response and are activated by receptor-ligand binding at the cell membrane. The latter initiates a signaling cascade within the cell, which finally triggers the coupling of the two key molecular components of the CRAC channel, namely the stromal interaction molecule, STIM, in the ER membrane and the plasma membrane Ca2+ ion channel, Orai. Ca2+ entry, established via STIM/Orai coupling, is essential for various immune cell functions, including cytokine release, proliferation, and cytotoxicity. In this review, we summarize the tools of synthetic biology that have been used so far to achieve precise control over the CRAC channel pathway and thus over downstream signaling events related to the immune response.
引用
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页数:38
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