Abstract
ABSTRACTThe control of all our motor outputs requires constant monitoring by proprioceptive sensory neurons (PSNs) that convey continuous muscle sensory inputs to the spinal motor network. Yet the molecular programs that control the establishment of this sensorimotor circuit remain largely unknown. The transcription factor RUNX3 is essential for the early steps of PSNs differentiation, making it difficult to study its role during later aspects of PSNs specification. Here, we conditionally inactivate Runx3 in PSNs after peripheral innervation and identify that RUNX3 is necessary for maintenance of cell identity of only a subgroup of PSNs, without discernable cell death. RUNX3 also controls the sensorimotor connection between PSNs and motor neurons at limb level, with muscle-by-muscle variable sensitivities to the loss of Runx3 that correlate with levels of RUNX3 in PSNs. Finally, we find that muscles and neurotrophin 3 signaling are necessary for maintenance of RUNX3 expression in PSNs. Hence, a transcriptional regulator that is crucial for specifying a generic PSN type identity after neurogenesis is later regulated by target muscle-derived signals to contribute to the specialized aspects of the sensorimotor connection selectivity.
Highlights
Introductionproprioceptive sensory neurons (PSNs) are identified by their specific co-expression of the runt related transcription factor RUNX3, tropomyosin receptor kinase C (TRKC, receptor for neurotrophin 3, NT3; known as Ntrk3), the ETS transcription factor ER81, parvalbumin (PV) and the vesicular glutamate transporter 1 (VGLUT1) (Oliveira et al, 2003; Lallemend and Ernfors, 2012)
The expression of factors necessary for the proper development and function of proprioceptive sensory neurons (PSNs), such as ER81 and TRKC, and of the marker PV were all downregulated in P0 AdvCre;Runx3fl/fl dorsal root ganglia (DRG) compared with Runx3fl/fl control mice (Fig. 1F-K)
These results show that expression of RUNX3 in late embryonic DRG neurons is necessary for maintaining cell identity of a subgroup of PSNs
Summary
PSNs are identified by their specific co-expression of the runt related transcription factor RUNX3, tropomyosin receptor kinase C (TRKC, receptor for neurotrophin 3, NT3; known as Ntrk3), the ETS transcription factor ER81, parvalbumin (PV) and the vesicular glutamate transporter 1 (VGLUT1) (Oliveira et al, 2003; Lallemend and Ernfors, 2012). They terminate in muscles and innervate the Golgi tendon organ (GTO) (Ib PSNs) and muscle spindles (MSs) (Ia and II PSNs). Genetic manipulation of signaling pathways or transcription factors affecting the afferent outgrowth and muscle targeting of PSNs often results in a lack of sensorimotor connections
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