4.3 Article

Classic cadherin expressions balance postnatal neuronal positioning and dendrite dynamics to elaborate the specific cytoarchitecture of the mouse cortical area

期刊

NEUROSCIENCE RESEARCH
卷 105, 期 -, 页码 49-64

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neures.2015.09.006

关键词

Classic cadherins; Cortical arealization; In utero electroporation; Somatosensory barrel; Neuronal activity dependent regulation

资金

  1. Intramural Research Grant for Neurological and Psychiatric Disorders of NCNP [24-12, 26-9, 27-7]
  2. JSPS [24300130]
  3. Takeda Science Foundation
  4. Grants-in-Aid for Scientific Research [16K10004, 15H04268, 16H06528, 15H01304, 15K14337] Funding Source: KAKEN

向作者/读者索取更多资源

A unique feature of the mammalian cerebral cortex is in its tangential parcellation via anatomical and functional differences. However, the cellular and/or molecular machinery involved in cortical arealization remain largely unknown. Here we map expression profiles of classic cadherins in the postnatal mouse barrel field of the primary somatosensory area (S1BF) and generate a novel bacterial artificial chromosome transgenic (BAC-Tg) mouse line selectively illuminating nuclei of cadherin-6 (Cdh6)-expressing layer IV barrel neurons to confirm that tangential cellular assemblage of S1 BF is established by postnatal day 5 (P5). When we electroporate the cadherins expressed in both barrel neurons and thalamo-cortical axon (TCA) terminals limited to the postnatal layer IV neurons, S1BF cytoarchitecture is disorganized with excess elongation of dendrites at P7. Upon delivery of dominant negative molecules for all classic cadherins, tangential cellular positioning and biased dendritic arborization of barrel neurons are significantly altered. These results underscore the value of classic cadherin-mediated sorting among neuronal cell bodies, dendrites and TCA terminals in postnatally elaborating the S1 BF-specific tangential cytoarchitecture. Additionally, how the protocortex machinery affects classic cadherin expression profiles in the process of cortical arealization is examined and discussed. (C) 2015 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Multidisciplinary Sciences

Novel EGFP reporter cell and mouse models for sensitive imaging and quantification of exon skipping

Yuko Hara, Yoshitaka Mizobe, Yukiko U. Inoue, Yasumasa Hashimoto, Norio Motohashi, Yoshiaki Masaki, Kohji Seio, Shin'ichi Takeda, Tetsuya Nagata, Matthew J. A. Wood, Takayoshi Inoue, Yoshitsugu Aoki

SCIENTIFIC REPORTS (2020)

Article Multidisciplinary Sciences

DSCAM regulates delamination of neurons in the developing midbrain

Nariko Arimura, Mako Okada, Shinichiro Taya, Ken-ichi Dewa, Akiko Tsuzuki, Hirotomo Uetake, Satoshi Miyashita, Koichi Hashizume, Kazumi Shimaoka, Saki Egusa, Tomoki Nishioka, Yuchio Yanagawa, Kazuhiro Yamakawa, Yukiko U. Inoue, Takayoshi Inoue, Kozo Kaibuchi, Mikio Hoshino

SCIENCE ADVANCES (2020)

Article Biology

Redundant type II cadherins define neuroepithelial cell states for cytoarchitectonic robustness

Kou Hiraga, Yukiko U. Inoue, Junko Asami, Mayuko Hotta, Yuki Morimoto, Shoji Tatsumoto, Mikio Hoshino, Yasuhiro Go, Takayoshi Inoue

COMMUNICATIONS BIOLOGY (2020)

Article Cell Biology

An Optimized Preparation Method for Long ssDNA Donors to Facilitate Quick Knock-In Mouse Generation

Yukiko U. Inoue, Yuki Morimoto, Mayumi Yamada, Ryosuke Kaneko, Kazumi Shimaoka, Shinji Oki, Mayuko Hotta, Junko Asami, Eriko Koike, Kei Hori, Mikio Hoshino, Itaru Imayoshi, Takayoshi Inoue

Summary: Fluorescent reporter mouse lines and Cre/Flp recombinase driver lines are essential for investigating molecular functions in vivo. The study reverified and optimized the phospho-PCR method to obtain highly pure long ssDNAs for knock-in mouse generation, enabling successful generation of knock-in mice through microinjection and electroporation methods, thus broadening its applicability.
Article Anatomy & Morphology

Detection of REST expression in the testis using epitope-tag knock-in mice generated by genome editing

Ryuichi Kimura, Yukiko U. Inoue, Takako Kikkawa, Misako Tatehana, Yuki Morimoto, Hitoshi Inada, Shinya Oki, Takayoshi Inoue, Noriko Osumi

Summary: The study confirmed the expression and localization of REST in the early stages of spermatogenesis, specifically in spermatogonia and Sertoli cells. This suggests that REST may modulate the epigenetic state of male germline cells, with implications for neurodevelopmental and age-related disorders. The knock-in mouse model generated in this study could be valuable for exploring REST-associated molecular mechanisms further.

DEVELOPMENTAL DYNAMICS (2022)

Article Multidisciplinary Sciences

A novel RyR1-selective inhibitor prevents and rescues sudden death in mouse models of malignant hyperthermia and heat stroke

Toshiko Yamazawa, Takuya Kobayashi, Nagomi Kurebayashi, Masato Konishi, Satoru Noguchi, Takayoshi Inoue, Yukiko U. Inoue, Ichizo Nishino, Shuichi Mori, Hiroto Iinuma, Noriaki Manaka, Hiroyuki Kagechika, Arkady Uryash, Jose Adams, Jose R. Lopez, Xiaochen Liu, Christine Diggle, Paul D. Allen, Sho Kakizawa, Keigo Ikeda, Bangzhong Lin, Yui Ikemi, Kazuto Nunomura, Shinsaku Nakagawa, Takashi Sakurai, Takashi Murayama

Summary: The study shows that an oxolinic acid-derivative RyR1 inhibitor can effectively prevent and treat various malignant hyperthermia (MH) and heat stroke mouse models.

NATURE COMMUNICATIONS (2021)

Article Cell Biology

A new mouse model of Ehlers-Danlos syndrome generated using CRISPR/Cas9-mediated genomic editing

Yuko Nitahara-Kasahara, Shuji Mizumoto, Yukiko U. Inoue, Shota Saka, Guillermo Posadas-Herrera, Aki Nakamura-Takahashi, Yuki Takahashi, Ayana Hashimoto, Kohei Konishi, Shinji Miyata, Chiaki Masuda, Emi Matsumoto, Yasunobu Maruoka, Takahiro Yoshizawa, Toshiki Tanase, Takayoshi Inoue, Shuhei Yamada, Yoshihiro Nomura, Shin'ichi Takeda, Atsushi Watanabe, Tomoki Kosho, Takashi Okada

Summary: Researchers generated mouse models for musculocontractural Ehlers-Danlos syndrome (mcEDS) through CRISPR/Cas9 genome editing, revealing pathophysiological features such as growth impairment, skin fragility, and muscle-related phenotypes caused by depletion of dermatan sulfate (DS). This study provides insights into the pathophysiology of mcEDS and may contribute to the development of novel treatment strategies.

DISEASE MODELS & MECHANISMS (2021)

Article Cell Biology

Myopathy Associated With Dermatan Sulfate-Deficient Decorin and Myostatin in Musculocontractural Ehlers-Danlos Syndrome: A Mouse Model Investigation

Yuko Nitahara-Kasahara, Guillermo Posadas-Herrera, Shuji Mizumoto, Aki Nakamura-Takahashi, Yukiko U. Inoue, Takayoshi Inoue, Yoshihiro Nomura, Shin'ichi Takeda, Shuhei Yamada, Tomoki Kosho, Takashi Okada

Summary: Deficiency of dermatan sulfate in mcEDS causes pathological distribution and functional abnormalities of decorin in the skeletal muscle, leading to disturbances in muscle myogenesis.

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2021)

Article Neurosciences

Targeting Neurons with Functional Oxytocin Receptors: A Novel Set of Simple Knock-In Mouse Lines for Oxytocin Receptor Visualization and Manipulation

Yukiko U. Inoue, Hideki Miwa, Kei Hori, Ryosuke Kaneko, Yuki Morimoto, Eriko Koike, Junko Asami, Satoshi Kamijo, Mitsuhiko Yamada, Mikio Hoshino, Takayoshi Inoue

Summary: This study utilized advanced genome editing techniques to generate a series of knock-in mouse lines, preserving the endogenous transcriptional regulations of the Oxtr gene. By using epitope tagging strategy and specific antibodies, the distribution of Oxtr protein on the neural membrane was visualized for the first time. Additionally, the expression of TdTomato reporter gene, Cre recombinase, and inducible Cre-ERT2 was successfully induced in Oxtr-expressing neurons. These tools provide valuable resources for future functional studies in Oxt-responsive neurons.

ENEURO (2022)

Article Multidisciplinary Sciences

Heat-hypersensitive mutants of ryanodine receptor type 1 revealed by microscopic heating

Kotaro Oyama, Vadim Zeeb, Toshiko Yamazawa, Nagomi Kurebayashi, Fuyu Kobirumaki-Shimozawa, Takashi Murayama, Hideto Oyamada, Satoru Noguchi, Takayoshi Inoue, Yukiko U. Inoue, Ichizo Nishino, Yoshie Harada, Norio Fukuda, Shin'ichi Ishiwata, Madoka Suzuki

Summary: This study investigates the relationship between mutant Ryanodine receptor type 1 (RyR1) and malignant hyperthermia (MH) using an optically controlled local heat-pulse method. The results show that RyR1 mutants are more heat sensitive and induce intracellular calcium bursts through heat-induced calcium release (HICR). HICR is also observed in skeletal muscles. This study highlights the complexity of MH and the positive feedback of HICR in thermogenesis in MH patients.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2022)

Article Multidisciplinary Sciences

Humanized substitutions of Vmat1 in mice alter amygdala-dependent behaviors associated with the evolution of anxiety

Daiki X. Sato, Yukiko U. Inoue, Nahoko Kuga, Satoko Hattori, Kensaku Nomoto, Yuki Morimoto, Giovanni Sala, Hideo Hagihara, Takefumi Kikusui, Takuya Sasaki, Yuji Ikegaya, Tsuyoshi Miyakawa, Takayoshi Inoue, Masakado Kawata

Summary: This study introduces human-specific mutations into mice and investigates their impact on behavior, neurophysiology, and molecular level. The results show that the introduction of the Ile mutation leads to reduced anxiety-related traits and altered oscillatory activity in the amygdala under anxiogenic conditions. Transcriptome analysis confirms changes in gene expression in the amygdala, further supporting the observed phenotypes.

ISCIENCE (2022)

Article Physiology

Mice with R2509C-RYR1 mutation exhibit dysfunctional Ca2+ dynamics in primary skeletal myocytes

Yoshitaka Tsuboi, Kotaro Oyama, Fuyu Kobirumaki-Shimozawa, Takashi Murayama, Nagomi Kurebayashi, Toshiaki Tachibana, Yoshinobu Manome, Emi Kikuchi, Satoru Noguchi, Takayoshi Inoue, Yukiko U. Inoue, Ichizo Nishino, Shuichi Mori, Ryosuke Ishida, Hiroyuki Kagechika, Madoka Suzuki, Norio Fukuda, Toshiko Yamazawa

Summary: The R2509C mutation in RYR1 causes dysfunctional calcium dynamics in a mutant-gene dose-dependent manner in skeletal muscles, leading to MH-like episodes in heterozygous mice and embryonic lethality in homozygous mice.

JOURNAL OF GENERAL PHYSIOLOGY (2022)

暂无数据