Leiter der Forschungsgruppe

Dr. Xin Yu
Dr. Xin Yu
Phone: +49 7071 601-740
Fax: +49 7071 601-701


Translational Neuroimaging and Neural Control

To understand how brain functions at the molecular, cellular and circuit levels, and eventually to gain control of the brain is the ultimate goal.

Fig 1.Decipher the central processing unit

The focus of this research group is to identify the primary brain nuclei potentially contributing to the switch of coma to awake states in the rat brain. Genetic tools and electrochemical recordings will be combined with fiber optic imaging and high field fMRI to study the altered brain function from the levels of molecules, to cells, and eventually to neurovascular circuits. We are expecting to translate the knowledge acquired from the rodent brain to lead specific neural control for therapies of coma patients.

We will test a central hypothesis that there is a “core switch”, which can be modulated to ameliorate the coma state of the brain. The focus of the research group is to decipher the biological feature of the “core switch”. Small animal fMRI allows us to map the global functional changes from multiple brain nuclei at different states. This provides us critical guide to target the potential candidate brain regions, of which the strategy has been successfully implemented in our previous work1. The specific cellular and molecular features of the functional changes detected by fMRI can be further studied by fiber optic/electrochemical recordings with optogenetic tools.

Here, we are going to establish several key multi-modal imaging schemes.

1.Mapping the “single unit” of the neurovascular coupling2,3

a.We are mapping the fMRI signal propagation from single arterioles to adjacent single venules in the deep cortex of rats.

Fig 2. The high spatial and temporal fMRI mapping S1 cortex. Single venules were detected in the dark voxels and single arterioles were detected in the bright voxels.Both BOLD (red color-coded) and CBV (blue-color coded) fMRI signal were detected at each voxels (150x150x500µm) at 100 ms.

b.Apply optogenetics and calcium fiber optic recordings to study the neuronal signal propagation from neuron to glia.
c.Apply siRNA to silence specific signaling molecules from neuron to vessel.

2.Building up an fMRI-based biofeedback brain-computer interface to use the recorded fMRI signal to control/modulate the brain function.

3.Introduce cell-specific neural control scheme at deep brain nuclei to modulate the brain states.

4.Develop sensors to detect neuromodulators or vasodilators in vivo (in collaborative scheme for electrochemical recordings or chemistry synthesis).

1.Yu, X. et al. Neuron 74, 731-742 (2012).
2.Yu, X. et al. NeuroImage 59, 1451-1460 (2012).
3. Yu, X., Qian, C., Chen, D.Y., Dodd, S.J. & Koretsky, A.P. Nature methods 11, 55-58 (2014).
Last updated: Mittwoch, 09.11.2016