TY - JOUR
T1 - Phase-Sensitive Measurements of Depth-Dependent Signal Transduction in the Inner Plexiform Layer
AU - Pfäffle, Clara
AU - Spahr, Hendrik
AU - Gercke, Katharina
AU - Puyo, Léo
AU - Höhl, Svea
AU - Melenberg, David
AU - Miura, Yoko
AU - Hüttmann, Gereon
AU - Hillmann, Dierck
N1 - Publisher Copyright:
Copyright © 2022 Pfäffle, Spahr, Gercke, Puyo, Höhl, Melenberg, Miura, Hüttmann and Hillmann.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - Non-invasive spatially resolved functional imaging in the human retina has recently attracted considerable attention. Particularly functional imaging of bipolar and ganglion cells could aid in studying neuronal activity in humans, including an investigation of processes of the central nervous system. Recently, we imaged the activity of the inner neuronal layers by measuring nanometer-size changes of the cells within the inner plexiform layer (IPL) using phase-sensitive optical coherence tomography (OCT). In the IPL, there are connections between the neuronal cells that are dedicated to the processing of different aspects of the visual information, such as edges in the image or temporal changes. Still, so far, it was not possible to assign functional changes to single cells or cell classes in living humans, which is essential for studying the vision process. One characteristic of signal processing in the IPL is that different aspects of the visual impression are only processed in specific sub-layers (strata). Here, we present an investigation of these functional signals for three different sub-layers in the IPL with the aim to separate different properties of the visual signal processing. Whereas the inner depth-layer, closest to the ganglion cells, exhibits an increase in the optical path length, the outer depth-layer, closest to the bipolar cell layer, exhibits a decrease in the optical path length. Additionally, we found that the central depth is sensitive to temporal changes, showing a maximum response at a stimulation frequency of around 12.5 Hz. The results demonstrate that the signals from different cell types can be distinguished by phase-sensitive OCT.
AB - Non-invasive spatially resolved functional imaging in the human retina has recently attracted considerable attention. Particularly functional imaging of bipolar and ganglion cells could aid in studying neuronal activity in humans, including an investigation of processes of the central nervous system. Recently, we imaged the activity of the inner neuronal layers by measuring nanometer-size changes of the cells within the inner plexiform layer (IPL) using phase-sensitive optical coherence tomography (OCT). In the IPL, there are connections between the neuronal cells that are dedicated to the processing of different aspects of the visual information, such as edges in the image or temporal changes. Still, so far, it was not possible to assign functional changes to single cells or cell classes in living humans, which is essential for studying the vision process. One characteristic of signal processing in the IPL is that different aspects of the visual impression are only processed in specific sub-layers (strata). Here, we present an investigation of these functional signals for three different sub-layers in the IPL with the aim to separate different properties of the visual signal processing. Whereas the inner depth-layer, closest to the ganglion cells, exhibits an increase in the optical path length, the outer depth-layer, closest to the bipolar cell layer, exhibits a decrease in the optical path length. Additionally, we found that the central depth is sensitive to temporal changes, showing a maximum response at a stimulation frequency of around 12.5 Hz. The results demonstrate that the signals from different cell types can be distinguished by phase-sensitive OCT.
UR - http://www.scopus.com/inward/record.url?scp=85132808950&partnerID=8YFLogxK
U2 - 10.3389/fmed.2022.885187
DO - 10.3389/fmed.2022.885187
M3 - Journal articles
C2 - 35721092
AN - SCOPUS:85132808950
SN - 2296-858X
VL - 9
SP - 885187
JO - Frontiers in medicine
JF - Frontiers in medicine
M1 - 885187
ER -