TY - JOUR
T1 - Activity dependent modulation of glial gap junction coupling in the thalamus
AU - Baum, Paula
AU - Beinhauer, Anna
AU - Zirwes, Lara
AU - Loenneker, Linda
AU - Jabs, Ronald
AU - Narayanan, Rajeevan T.
AU - Oberlaender, Marcel
AU - Seifert, Gerald
AU - Kettenmann, Helmut
AU - Steinhäuser, Christian
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/10/18
Y1 - 2024/10/18
N2 - Astrocytes and oligodendrocytes in the ventrobasal thalamus are electrically coupled through gap junctions. We have previously shown that these cells form large panglial networks, which have a key role in the transfer of energy substrates to postsynapses for sustaining neuronal activity. Here, we show that the efficiency of these transfer networks is regulated by synaptic activity: preventing the generation and propagation of action potentials resulted in reduced glial coupling. Systematic analyses of mice deficient for individual connexin isoforms revealed that oligodendroglial Cx32 and Cx47 are the targets of this modulation. Importantly, we show that during a critical time window, sensory deprivation through whisker trimming reduces the efficiency of the glial transfer networks also in vivo. Together with our previous results the current findings indicate that neuronal activity and provision of energy metabolites through panglial coupling are interdependent events regulated in a bidirectional manner.
AB - Astrocytes and oligodendrocytes in the ventrobasal thalamus are electrically coupled through gap junctions. We have previously shown that these cells form large panglial networks, which have a key role in the transfer of energy substrates to postsynapses for sustaining neuronal activity. Here, we show that the efficiency of these transfer networks is regulated by synaptic activity: preventing the generation and propagation of action potentials resulted in reduced glial coupling. Systematic analyses of mice deficient for individual connexin isoforms revealed that oligodendroglial Cx32 and Cx47 are the targets of this modulation. Importantly, we show that during a critical time window, sensory deprivation through whisker trimming reduces the efficiency of the glial transfer networks also in vivo. Together with our previous results the current findings indicate that neuronal activity and provision of energy metabolites through panglial coupling are interdependent events regulated in a bidirectional manner.
KW - cellular neuroscience
KW - molecular neuroscience
UR - http://www.scopus.com/inward/record.url?scp=85207788303&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85207788303&partnerID=8YFLogxK
U2 - 10.1016/j.isci.2024.111043
DO - 10.1016/j.isci.2024.111043
M3 - Article
AN - SCOPUS:85207788303
SN - 2589-0042
VL - 27
SP - 1
EP - 15
JO - iScience
JF - iScience
IS - 10
M1 - 111043
ER -