Cerebrospinal fluid-contacting neuron tracing reveals structural and functional connectivity for locomotion in the mouse spinal cord.
Yuka NakamuraMiyuki KurabeMami MatsumotoTokiharu SatoSatoshi MiytashitaKana HoshinaYoshinori KamiyaKazuki TainakaHitoshi MatsuzawaNobuhiko OhnoMasaki UenoPublished in: eLife (2023)
Cerebrospinal fluid-contacting neurons (CSF-cNs) are enigmatic mechano- or chemosensory cells lying along the central canal of the spinal cord. Recent studies in zebrafish larvae and lampreys have shown that CSF-cNs control postures and movements via spinal connections. However, the structures, connectivity, and functions in mammals remain largely unknown. Here we developed a method to genetically target mouse CSF-cNs that highlighted structural connections and functions. We first found that intracerebroventricular injection of adeno-associated virus with a neuron-specific promoter and Pkd2l1-Cre mice specifically labeled CSF-cNs. Single-cell labeling of 71 CSF-cNs revealed rostral axon extensions of over 1800 μm in unmyelinated bundles in the ventral funiculus and terminated on CSF-cNs to form a recurrent circuitry, which was further determined by serial electron microscopy and electrophysiology. CSF-cNs were also found to connect with axial motor neurons and premotor interneurons around the central canal and within the axon bundles. Chemogenetic CSF-cNs inactivation reduced speed and step frequency during treadmill locomotion. Our data revealed the basic structures and connections of mouse CSF-cNs to control spinal motor circuits for proper locomotion. The versatile methods developed in this study will contribute to further understanding of CSF-cN functions in mammals.
Keyphrases
- spinal cord
- cerebrospinal fluid
- blood brain barrier
- functional connectivity
- single cell
- spinal cord injury
- neuropathic pain
- metabolic syndrome
- machine learning
- adipose tissue
- transcription factor
- electron microscopy
- multiple sclerosis
- gene expression
- squamous cell carcinoma
- computed tomography
- cell death
- rna seq
- cell proliferation
- electronic health record
- skeletal muscle
- positron emission tomography
- endoplasmic reticulum stress
- big data
- pet imaging
- pet ct