Molecular determinants specifying diversity of neurons in the visual system during development
Molecular determinants specifying diversity of neurons in the visual system during development
批准号:
18500291
负责人:
KAWASAKI Hiroshi
金额:
$2.57万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007
中文摘要
视觉信息由视网膜检测,并通过外侧膝状核(LGN)传递到初级视觉皮层,这是丘脑核之一。这条初级视觉通路包含多种神经元,它们选择性地对特定类型的视觉刺激作出反应,如M细胞和P细胞分别对视觉刺激的空间信息和颜色/形状信息作出反应。这些神经元在视觉系统中形成柱状结构或分层结构。神经元的多样性和这些神经元的三维结构被认为是有效的视觉处理的重要因素。然而,神经元身份和三维结构形成的分子机制在很大程度上仍然未知。我们研究了LGN中M细胞分化的机制。在此之前,我们已经发现PCP4/PEP-19在M细胞中表达,并使用PCP4作为M细胞标记物,我们研究了自发视网膜活性在M细胞分化中的重要性。我们在出生后双眼注射抑制自发视网膜活性的依比替丁,并采用原位杂交技术检测llgn中PCP4的表达。我们发现PCP4的表达在经依比替定处理的动物中没有受到影响,这表明M细胞分化不需要自发的视网膜活动。此外,PCP4在去核动物中表达正常。这些结果表明,M细胞分化不仅需要自发的视网膜活动,还需要各种视网膜输入。LGN不仅接受来自视网膜的输入,还接受来自视觉皮层和脑干的输入,这可能驱动M细胞分化。因此,我们分离LGN并进行体外培养。有趣的是,我们发现M细胞分化发生在培养的LGN中,这表明LGN分化可以在没有其他脑区输入的情况下进行。值得注意的是,我们的实验只使用了一种M细胞标记物。我们需要使用额外的M细胞标记物来确认我们的结果。少
英文摘要
Visual information is detected by the retina, and transferred to the primary visual cortex via the lateral geniculate nucleus (LGN), which is one of thalamic nuclei. This primary visual pathway contains a variety of neurons, which selectively respond to specific types of visual stimuli, such as M cells and P cells which respond to spatial information and color/shape information of visual stimuli, respectively. These neurons form column-like structures or layered structures in the visual system. The variety of neurons and 3D structures of these neurons are considered to be important for efficient visual processing. However, molecular mechanisms underlying specification of neuronal identities and formation of 3D structures are still largely unknown.We have examined the mechanisms of M cell differentiation in the LGN. Previously, we have found that PCP4/PEP-19 is expressed in M cells, and using PCP4 as an M cell marker, we examined the importance of spontaneous retinal activity in M cell … More differentiation. We binocularly injected epibatidine, which suppresses spontaneous retinal activity, into the two eyes just after birth, and examined the expression of PCP4 in the LGN using in situ hybridization. We found that the expression of PCP4 was not affected in epibatidine-treated animals, suggesting that M cell differentiation does not require spontaneous retinal activity. Moreover, PCP4 expression was normal in enucleated animals. These results suggest that M cell differentiation does not require not only spontaneous retinal activity, but also all kinds of retinal inputs.LGN receives inputs not only from the retina but also from the visual cortex and the brainstem, which may drive M cell differentiation. We therefore isolated LGN and cultured it in vitro. Interestingly, we found that M cell differentiation occurred in the cultured LGN, suggesting that LGN differentiation can proceed without inputs from other brain regions. It should be noted that we have performed our experiments using only one kind of M cell marker. We need to confirm our results using additional M cell markers. Less
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フェレットを用いた高次視覚神経系の形成機構解析
利用雪貂分析高级视觉神经系统的形成机制
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[岩井玲奈, 河崎洋志]
通讯作者:
河崎洋志
Developmental processes in the ferret LGN independent of input from retina and visual cortex
雪貂 LGN 的发育过程独立于视网膜和视觉皮层的输入
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Lena Iwai, Hiroshi Kawasaki]
通讯作者:
Hiroshi Kawasaki
The role of oligodendrocytes in the critical period regulation in the primary somatosensory cortex
少突胶质细胞在初级体感皮层关键期调节中的作用
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Tomohisa Toda, Itaru Hayakawa, Yutaka Matsubayashi, Kenji Tanaka, Kazuhiro Ikenaka, Qing R. Lu, Hiroshi Kawasaki]
通讯作者:
Hiroshi Kawasaki
カルモデュリンはPCP4/PEP-19により細胞質に繋留され、細胞内カルシウムイオン濃度の上昇によってリリースされる
钙调蛋白通过 PCP4/PEP-19 束缚在细胞质上,并通过增加细胞内钙离子浓度来释放。
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[松林完, 河崎洋志]
通讯作者:
河崎洋志
フェレット外側膝状体のスライス培養を用いた神経入力非依存的な分化過程の解析
利用雪貂外侧膝状体切片培养分析神经输入独立分化过程
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[岩井玲奈, 河崎洋志]
通讯作者:
河崎洋志
共 19 条
Mechanisms of brain formation regulated by birth
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批准号:25640032
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项目类别:Grant-in-Aid for Challenging Exploratory Research
-
资助金额:$2.58万
-
财政年份:2013
-
负责人:KAWASAKI Hiroshi
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依托单位:
Development of a New Model for Atopic Dermatitis Using Filaggrin Mutant Mice
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批准号:21791095
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项目类别:Grant-in-Aid for Young Scientists (B)
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资助金额:$2.75万
-
财政年份:2009
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负责人:KAWASAKI Hiroshi
-
依托单位:
Structure and function of multifunctional protein complex regulating cell polarity
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批准号:21510228
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.91万
-
财政年份:2009
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负责人:KAWASAKI Hiroshi
-
依托单位:
Shape reconstruction from single camera and line lasers
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批准号:19700157
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项目类别:Grant-in-Aid for Young Scientists (B)
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资助金额:$2.38万
-
财政年份:2007
-
负责人:KAWASAKI Hiroshi
-
依托单位:
The role of Integrin-downstream signaling molecules in the expression of chemokine receptors
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批准号:18591103
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.34万
-
财政年份:2006
-
负责人:KAWASAKI Hiroshi
-
依托单位:
Structural and functional analysis on protein complex of ubiquitin-proteasome system
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批准号:15580308
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.11万
-
财政年份:2003
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负责人:KAWASAKI Hiroshi
-
依托单位:
IL-12-mediated regulation of human chemokine receptor function
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批准号:14570405
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项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$1.92万
-
财政年份:2002
-
负责人:KAWASAKI Hiroshi
-
依托单位:
The ummunobiology of IL 12 receptors expressed on human dendritic cells
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批准号:12670414
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.18万
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财政年份:2000
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负责人:KAWASAKI Hiroshi
-
依托单位:
Physiology and pathophysiology of human Interleukin 12 receptor system
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批准号:10670408
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$0.64万
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财政年份:1998
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负责人:KAWASAKI Hiroshi
-
依托单位:
Activation and substrate recognition mechanism of calpain
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批准号:08680668
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.47万
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财政年份:1996
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负责人:KAWASAKI Hiroshi
-
依托单位:
Structural and Functional Analysis of Human Interleukin-12 Receptor
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批准号:08670514
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.41万
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财政年份:1996
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负责人:KAWASAKI Hiroshi
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依托单位:
海外基金