TY - JOUR
T1 - Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons
AU - Kohler, Matthias
AU - Bengtsson, Fredrik
AU - Stratmann, Philipp
AU - Röhrbein, Florian
AU - Knoll, Alois
AU - Albu-Schäffer, Alin
AU - Jörntell, Henrik
PY - 2022/4
Y1 - 2022/4
N2 - The spinal cord is engaged in all forms of motor performance but its functions are far from understood. Because network connectivity defines function, we explored the connectivity of muscular, tendon, and tactile sensory inputs among a wide population of spinal interneurons in the lower cervical segments. Using low noise intracellular whole cell recordings in the decerebrated, non-anesthetized cat in vivo, we could define mono-, di-, and trisynaptic inputs as well as the weights of each input. Whereas each neuron had a highly specific input, and each indirect input could moreover be explained by inputs in other recorded neurons, we unexpectedly also found the input connectivity of the spinal interneuron population to form a continuum. Our data hence contrasts with the currently widespread notion of distinct classes of interneurons. We argue that this suggested diversified physiological connectivity, which likely requires a major component of circuitry learning, implies a more flexible functionality.
AB - The spinal cord is engaged in all forms of motor performance but its functions are far from understood. Because network connectivity defines function, we explored the connectivity of muscular, tendon, and tactile sensory inputs among a wide population of spinal interneurons in the lower cervical segments. Using low noise intracellular whole cell recordings in the decerebrated, non-anesthetized cat in vivo, we could define mono-, di-, and trisynaptic inputs as well as the weights of each input. Whereas each neuron had a highly specific input, and each indirect input could moreover be explained by inputs in other recorded neurons, we unexpectedly also found the input connectivity of the spinal interneuron population to form a continuum. Our data hence contrasts with the currently widespread notion of distinct classes of interneurons. We argue that this suggested diversified physiological connectivity, which likely requires a major component of circuitry learning, implies a more flexible functionality.
KW - Behavioral neuroscience
KW - Biological sciences
KW - Cellular neuroscience
U2 - 10.1016/j.isci.2022.104083
DO - 10.1016/j.isci.2022.104083
M3 - Article
C2 - 35372805
AN - SCOPUS:85127128629
SN - 2589-0042
VL - 25
JO - iScience
JF - iScience
IS - 4
M1 - 104083
ER -