Petrushenko Olena A, Stratiievska Anastasiiya O, Petrushenko Mariia O, Lukyanetz Elena A
Department of Biophysics of Ion Channels, Bogomoletz Institute of Physiology, Kyiv, Ukraine.
Front Cell Neurosci. 2023 Jun 1;17:1192780. doi: 10.3389/fncel.2023.1192780. eCollection 2023.
TRPV1 channels are responsible for detecting noxious stimuli such as heat (>43°C), acid, and capsaicin. P2 receptors are involved in numerous functions of the nervous system, including its modulation and specific response to the application of ATP. In our experiments, we investigated the dynamics of calcium transients in DRG neurons associated with TRPV1 channel desensitization and the effect of activation of P2 receptors on this process.
We used DRG neurons from rats P7-8 after 1-2 days of culture to measure calcium transients by microfluorescence calcimetry using the fluorescent dye Fura-2 AM.
We have shown that DRG neurons of small (d < 22 μm) and medium (d = 24-35 μm) sizes differ in TRPV1 expression. Thus, TRPV1 channels are mainly present in small nociceptive neurons (59% of the studied neurons). Short-term sequential application of the TRPV1 channel agonist capsaicin (100nM) leads to the desensitization of TRPV1 channels by the type of tachyphylaxis. We identified three types of sensory neurons based on responses to capsaicin: (1) desensitized 37.5%, (2) non-desensitized 34.4%, and (3) insensitive 23.4% to capsaicin. It has also been shown that P2 receptors are present in all types of neurons according to their size. So, the responses to ATP were different in different-sized neurons. Applying ATP (0.1 mM) to the intact cell membrane after the onset of tachyphylaxis caused recovery of calcium transients in response to the addition of capsaicin in these neurons. The amplitude of the capsaicin response after reconstitution with ATP was 161% of the previous minimal calcium transient in response to capsaicin.
Significantly, the restoration of the amplitude of calcium transients under the ATP application is not associated with changes in the cytoplasmic pool of ATP because this molecule does not cross the intact cell membrane, thus, our results show the interaction between TRPV1 channels and P2 receptors. It is important to note that the restoration of the amplitude of calcium transients through TRPV1 channels after application of ATP was observed mainly in cells of 1-2 days of cultivation. Thus, the resensitization of capsaicin transients following P2 receptor activation may be associated with the regulation of the sensitivity of sensory neurons.
TRPV1通道负责检测有害刺激,如热(>43°C)、酸和辣椒素。P2受体参与神经系统的多种功能,包括其调节以及对ATP应用的特异性反应。在我们的实验中,我们研究了与TRPV1通道脱敏相关的背根神经节(DRG)神经元中钙瞬变的动力学,以及P2受体激活对这一过程的影响。
我们使用培养1 - 2天后的P7 - 8大鼠的DRG神经元,通过使用荧光染料Fura - 2 AM的显微荧光钙测定法来测量钙瞬变。
我们已经表明,小尺寸(d < 22μm)和中等尺寸(d = 24 - 35μm)的DRG神经元在TRPV1表达上存在差异。因此,TRPV1通道主要存在于小的伤害性神经元中(占所研究神经元的59%)。短期连续应用TRPV1通道激动剂辣椒素(100nM)会导致TRPV1通道出现快速脱敏。基于对辣椒素的反应,我们鉴定出三种类型的感觉神经元:(1)脱敏的占37.5%,(2)未脱敏的占34.4%,(3)对辣椒素不敏感的占23.4%。还表明,根据神经元大小,P2受体存在于所有类型的神经元中。因此,不同大小的神经元对ATP的反应不同。在快速脱敏开始后,将ATP(0.1 mM)应用于完整细胞膜会使这些神经元在添加辣椒素后钙瞬变恢复。用ATP重构后辣椒素反应的幅度是先前对辣椒素最小钙瞬变的161%。
重要的是,ATP应用下钙瞬变幅度的恢复与ATP的细胞质池变化无关,因为该分子不会穿过完整细胞膜,因此,我们的结果显示了TRPV1通道与P2受体之间的相互作用。需要注意的是,在应用ATP后通过TRPV1通道恢复钙瞬变幅度主要在培养1 - 2天的细胞中观察到。因此,P2受体激活后辣椒素瞬变的再敏化可能与感觉神经元敏感性的调节有关。