Dlk1 Promotes a Fast Motor Neuron Biophysical Signature Required for Peak Force Execution.

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Bibliographic Details
Title: Dlk1 Promotes a Fast Motor Neuron Biophysical Signature Required for Peak Force Execution.
Authors: Müller, Daniel, Cherukuri, Pitchaiah, Henningfeld, Kristine, Chor Hoon Poh, Wittler, Lars, Grote, Phillip, Schlüter, Oliver, Schmidt, Jennifer, Laborda, Jorge, Bauer, Steven R., Brownstone, Robert M., Marquardt, Till
Source: Science (pre-March 2025). 3/14/2014, Vol. 343 Issue 6176, p1264-1266. 3p.
Subjects: Motor neurons, Ligands (Biochemistry), Muscle motility, Notch protein genetics, Animal mechanics
Abstract: Motor neurons, which relay neural commands to drive skeletal muscle movements, encompass types ranging from "slow" to "fast," whose biophysical properties govern the timing, gradation, and amplitude of muscle force. Here we identify the noncanonical Notch ligand Delta-like homolog 1 (Dlk1) as a determinant of motor neuron functional diversification. Dlk1, expressed by ~30% of motor neurons, is necessary and sufficient to promote a fast biophysical signature in the mouse and chick. Dlk1 suppresses Notch signaling and activates expression of the K+ channel subunit Kcng4 to modulate delayed-rectifier currents. Dlk1 inactivation comprehensively shifts motor neurons toward slow biophysical and transcriptome signatures, while abolishing peak force outputs. Our findings provide insights into the development of motor neuron functional diversity and its contribution to the execution of movements. [ABSTRACT FROM AUTHOR]
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Database: Psychology and Behavioral Sciences Collection
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