Cell types, network homeostasis, and pathological compensation from a biologically plausible ion channel expression model.

Abstract:

:How do neurons develop, control, and maintain their electrical signaling properties in spite of ongoing protein turnover and perturbations to activity? From generic assumptions about the molecular biology underlying channel expression, we derive a simple model and show how it encodes an "activity set point" in single neurons. The model generates diverse self-regulating cell types and relates correlations in conductance expression observed in vivo to underlying channel expression rates. Synaptic as well as intrinsic conductances can be regulated to make a self-assembling central pattern generator network; thus, network-level homeostasis can emerge from cell-autonomous regulation rules. Finally, we demonstrate that the outcome of homeostatic regulation depends on the complement of ion channels expressed in cells: in some cases, loss of specific ion channels can be compensated; in others, the homeostatic mechanism itself causes pathological loss of function.

journal_name

Neuron

journal_title

Neuron

authors

O'Leary T,Williams AH,Franci A,Marder E

doi

10.1016/j.neuron.2014.04.002

subject

Has Abstract

pub_date

2014-05-21 00:00:00

pages

809-21

issue

4

eissn

0896-6273

issn

1097-4199

pii

S0896-6273(14)00292-X

journal_volume

82

pub_type

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