Person: Ji, Ni
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Publication Neuroendocrine modulation sustains the C. elegans forward motor state
(eLife Sciences Publications, Ltd, 2016) Lim, Maria A; Chitturi, Jyothsna; Laskova, Valeriya; Meng, Jun; Findeis, Daniel; Wiekenberg, Anne; Mulcahy, Ben; Luo, Linjiao; Li, Yan; Lu, Yangning; Hung, Wesley; Qu, Yixin; Ho, Chi-Yip; Holmyard, Douglas; Ji, Ni; McWhirter, Rebecca; Samuel, Aravi; Miller, David M; Schnabel, Ralf; Calarco, John A; Zhen, MeiNeuromodulators shape neural circuit dynamics. Combining electron microscopy, genetics, transcriptome profiling, calcium imaging, and optogenetics, we discovered a peptidergic neuron that modulates C. elegans motor circuit dynamics. The Six/SO-family homeobox transcription factor UNC-39 governs lineage-specific neurogenesis to give rise to a neuron RID. RID bears the anatomic hallmarks of a specialized endocrine neuron: it harbors near-exclusive dense core vesicles that cluster periodically along the axon, and expresses multiple neuropeptides, including the FMRF-amide-related FLP-14. RID activity increases during forward movement. Ablating RID reduces the sustainability of forward movement, a phenotype partially recapitulated by removing FLP-14. Optogenetic depolarization of RID prolongs forward movement, an effect reduced in the absence of FLP-14. Together, these results establish the role of a neuroendocrine cell RID in sustaining a specific behavioral state in C. elegans. DOI: http://dx.doi.org/10.7554/eLife.19887.001
Publication Pan-neuronal imaging in roaming Caenorhabditis elegans
(Proceedings of the National Academy of Sciences, 2015) Venkatachalam, Vivek; Ji, Ni; Wang, Xian-Ling; Clark, Christopher; Mitchell, James; Klein, Mason; Tabone, Christopher; Florman, Jeremy; Ji, Hongfei; Greenwood, Joel S.f.; Chisholm, Andrew; Srinivasan, Jagan; Alkema, Mark; Zhen, Mei; Samuel, AraviWe present an imaging system for pan-neuronal recording in crawling Caenorhabditis elegans. A spinning disk confocal microscope, modified for automated tracking of the C. elegans head ganglia, simultaneously records the activity and position of ∼80 neurons that coexpress cytoplasmic calcium indicator GCaMP6s and nuclear localized red fluorescent protein at 10 volumes per second. We developed a behavioral analysis algorithm that maps the movements of the head ganglia to the animal’s posture and locomotion. Image registration and analysis software automatically assigns an index to each nucleus and calculates the corresponding calcium signal. Neurons with highly stereotyped positions can be associated with unique indexes and subsequently identified using an atlas of the worm nervous system. To test our system, we analyzed the brainwide activity patterns of moving worms subjected to thermosensory inputs. We demonstrate that our setup is able to uncover representations of sensory input and motor output of individual neurons from brainwide dynamics. Our imaging setup and analysis pipeline should facilitate mapping circuits for sensory to motor transformation in transparent behaving animals such as C. elegans and Drosophila larva.