Wnt/β-catenin is required for proprioception by coordinating the multi-compartment development of muscle spindles

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Abstract

Proprioception is essential for the regulation of posture, movement, and musculoskeletal integrity. The muscle spindle, a mechanosensory organ composed of multiple specialized tissues, detects stretch and provides proprioceptive feedback. Despite its importance, the molecular mechanisms that orchestrate the development of the spindle components remain poorly understood. Here, we reveal the involvement of the Wnt/β-catenin pathway in muscle spindle development. We show that Wnt ligands and their Frizzled receptors are expressed in the developing spindle and that β-catenin is active throughout development in capsule cells and in bag2 intrafusal fibers. Embryonic deletion of β-catenin from capsule and intrafusal fibers induced widespread transcriptomic changes, which led to significant malformations, including impaired capsule cell differentiation, disrupted nuclear organization in intrafusal fibers, and disorganized proprioceptive nerve endings. Postnatal deletion of β-catenin from intrafusal fibers resulted in abnormal nerve endings and impaired proprioceptive function, indicating that the development of proprioceptive afferents is regulated by β-catenin through a non–cell-autonomous mechanism acting in bag2 fibers. Collectively, our findings position the Wnt/β-catenin pathway as a central regulator that acts through both cell-autonomous and non–cell-autonomous mechanisms to coordinate the development of the various spindle tissues into a functional organ.
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Abstract Proprioception is essential for the regulation of posture, movement, and musculoskeletal integrity. The muscle spindle, a mechanosensory organ composed of multiple specialized tissues, detects stretch and provides proprioceptive feedback. Despite its importance, the molecular mechanisms that orchestrate the development of the spindle components remain poorly understood. Here, we reveal the involvement of the Wnt/β-catenin pathway in muscle spindle development. We show that Wnt ligands and their Frizzled receptors are expressed in the developing spindle and that β-catenin is active throughout development in capsule cells and in bag2 intrafusal fibers. Embryonic deletion of β-catenin from capsule and intrafusal fibers induced widespread transcriptomic changes, which led to significant malformations, including impaired capsule cell differentiation, disrupted nuclear organization in intrafusal fibers, and disorganized proprioceptive nerve endings. Postnatal deletion of β-catenin from intrafusal fibers resulted in abnormal nerve endings and impaired proprioceptive function, indicating that the development of proprioceptive afferents is regulated by β-catenin through a non–cell-autonomous mechanism acting in bag2 fibers. Collectively, our findings position the Wnt/β-catenin pathway as a central regulator that acts through both cell-autonomous and non–cell-autonomous mechanisms to coordinate the development of the various spindle tissues into a functional organ. Competing Interest Statement The authors have declared no competing interest. Footnotes We added additional data and figures on behavioral test, revised the result and the discussion.

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