INSERM U1128, Laboratory of Neurophysiology and New Microscopy, Université Paris Descartes, Paris 75006, France.
INSERM U1128, Laboratory of Neurophysiology and New Microscopy, Université Paris Descartes, Paris 75006, France.
Neuron. 2018 Jul 25;99(2):362-375.e4. doi: 10.1016/j.neuron.2018.06.012. Epub 2018 Jun 21.
Functional hyperemia, a regional increase of blood flow triggered by local neural activation, is used to map brain activity in health and disease. However, the spatial-temporal dynamics of functional hyperemia remain unclear. Two-photon imaging of the entire vascular arbor in NG2-creERT2;GCaMP6f mice shows that local synaptic activation, measured via oligodendrocyte precursor cell (OPC) Ca signaling, generates a synchronous Ca drop in pericytes and smooth muscle cells (SMCs) enwrapping all upstream vessels feeding the activated synapses. Surprisingly, the onset timing, direction, and amplitude of vessel diameter and blood velocity changes vary dramatically from juxta-synaptic capillaries back to the pial arteriole. These results establish a precise spatial-temporal sequence of vascular changes triggered by neural activity and essential for the interpretation of blood-flow-based imaging techniques such as BOLD-fMRI.
功能充血是一种由局部神经激活引发的区域性血流增加,用于在健康和疾病状态下绘制大脑活动图谱。然而,功能充血的时空动力学仍不清楚。利用 NG2-creERT2;GCaMP6f 小鼠的全血管树双光子成像显示,局部突触激活(通过少突胶质前体细胞 (OPC) Ca 信号测量)会导致围绕所有上游血管的周细胞和血管平滑肌细胞 (SMC) 中的同步 Ca 下降,这些上游血管为激活的突触提供营养。令人惊讶的是,血管直径和血流速度变化的起始时间、方向和幅度从突触旁毛细血管到软脑膜小动脉变化巨大。这些结果建立了神经活动引发的血管变化的精确时空顺序,对于解释基于血流的成像技术(如 BOLD-fMRI)至关重要。