{"title":"Neuroarchitecture of the Central Complex in the Madeira Cockroach Rhyparobia maderae: Tangential Neurons","authors":"Stefanie Jahn, Vanessa Althaus, Ann-Katrin Seip, Saron Rotella, Jannik Heckmann, Mona Janning, Juliana Kolano, Aurelia Kaufmann, Uwe Homberg","doi":"10.1002/cne.70009","DOIUrl":null,"url":null,"abstract":"<p>Navigating in diverse environments to find food, shelter, or mating partners is an important ability for nearly all animals. Insects have evolved diverse navigational strategies to survive in challenging and unknown environments. In the insect brain, the central complex (CX) plays an important role in spatial orientation and directed locomotion. It consists of the protocerebral bridge (PB), the central body with upper (CBU) and lower division (CBL), and the paired noduli (NO). As shown in various insect species, the CX integrates multisensory cues, including sky compass signals, wind direction, and ego-motion to provide goal-directed vector output used for steering locomotion and flight. While most of these data originate from studies on day-active insects, less is known about night-active species such as cockroaches. Following our analysis of columnar and pontine neurons, the present study complements our investigation of the cellular architecture of the CX of the Madeira cockroach by analyzing tangential neurons. Based on single-cell tracer injections, we provide further details on the internal organization of the CX and distinguished 27 types of tangential neuron, including three types of neuron innervating the PB, six types of the CBL, and 18 types of the CBU. The anterior lip, a brain area unknown in flies and highly reduced in bees, and the crepine are strongly connected to the cockroach CBU in contrast to other insect species. One tangential neuron of the CBU revealed a direct connection between the mushroom bodies and the CBU.</p>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"532 12","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11632141/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70009","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Navigating in diverse environments to find food, shelter, or mating partners is an important ability for nearly all animals. Insects have evolved diverse navigational strategies to survive in challenging and unknown environments. In the insect brain, the central complex (CX) plays an important role in spatial orientation and directed locomotion. It consists of the protocerebral bridge (PB), the central body with upper (CBU) and lower division (CBL), and the paired noduli (NO). As shown in various insect species, the CX integrates multisensory cues, including sky compass signals, wind direction, and ego-motion to provide goal-directed vector output used for steering locomotion and flight. While most of these data originate from studies on day-active insects, less is known about night-active species such as cockroaches. Following our analysis of columnar and pontine neurons, the present study complements our investigation of the cellular architecture of the CX of the Madeira cockroach by analyzing tangential neurons. Based on single-cell tracer injections, we provide further details on the internal organization of the CX and distinguished 27 types of tangential neuron, including three types of neuron innervating the PB, six types of the CBL, and 18 types of the CBU. The anterior lip, a brain area unknown in flies and highly reduced in bees, and the crepine are strongly connected to the cockroach CBU in contrast to other insect species. One tangential neuron of the CBU revealed a direct connection between the mushroom bodies and the CBU.
期刊介绍:
Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states.
Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se.
JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.