Patterning Neurogenesis: Dynamics of signaling and gene regulation in Drosophila eye development

报告题目:Patterning Neurogenesis: Dynamics of signaling and gene regulation in Drosophila eye development
报告时间:8月4日 上午10点
报告地点:S2-102
报告专家:Prof. Nicholas Baker, Albert Einstein College of Medicine
联系人:韩敬东

 

Our research addresses mechanisms of growth and development in the fruitfly Drosophila melanogaster . Read more about our research interests here .


Dr. Nicholas E.Baker

Departments of Genetics

1300 Morris Park Avenue
Bronx, NY 10461
Tel: 718-430-28-54/55
nbaker@aecom.yu.edu

 

Overview:

Growth and Development of Drosophila

Much is known about the molecular biology of the cell, but many interesting processes in biology and medicine depend on populations of cells and the interactions between cells.  The fruitfly Drosophila melanogaster , in which advanced in vivo genetic mosaic techniques are available, can be used to investigate how cell-cell interactions contribute to body form and function.  We are elucidating the molecular mechanisms of neurogenesis, using molecular and genetic experiments as well as mathematical modeling to understand how certain cells are chose to differentiate into neural fates, and also how this is linked to terminal cell cycle withdrawal that maintains neurons in a post-mitotic state for the remainder of life.  These studies focus on the retina as an exemplary neural tissue, and help to understand both neural developmental defects and neurodegenerative conditions, since there is emerging evidence that neurodegenerative conditions including Alzheimer’s Disease, Huntington’s Disease, Ataxia Telangiectasia, stroke, AIDS-related dementia, and viral encephalitis are associated with inappropriate cell cycle activation by otherwise postmitotic neurons.
We are also seeking a comprehensive understanding of the phenomenon of cell competition, which is revealed when the organism eliminates cells that would survive were the whole organism the same genotype.  Even wild type cells can be out-competed by ‘super-competitor’ genotypes, such as cells that over-express myc, or cells mutated for certain tumor suppressor genes. Cell competition reveals a way that cell interactions can select the most favorable progenitor cells available, something that was not suspected prior to these chimera studies.   In rodents, cell competition is thought to explain how liver progenitor cells from young donors replace older host cells when liver regeneration is stimulated in chimeras.  Cell competition might occur during the development of cancer, since tumors normally differ genetically from normal cells.

Selected Publications

Tyler, D. and Baker, N.E. (2007).  Expanded and fat regulate growth and differentiation in the Drosophila eye through multiple signaling pathways.  Dev. Biol. , 305 , 187-201.
Firth, L.C., and Baker, N.E.  (2007).  Spitz from the retina regulates genes transcribed in the Second Mitotic Wave,  peripodial epithelium,  glia and plasmatocytes of the Drosophila eye imaginal disc.  Dev. Biol. , 307 , 521-538.
Li, W. and Baker, N.E. (2007)  Engulfment is required for cell competition.  Cell , 129 , 1215-1225.
Baker, N.E.   (2007)  Pattern formation and the spatial regulation of proliferation.  Curr. Opin. Genet. Dev . 17 , 287-293.
Li, W. and Baker,, N.E.   (2007)  The active role of corpse engulfment pathways during cell competition.  Fly 1, 274-278.
Pei , Z. and Baker, N.E. (2008).  Competition between Delta and the Abruptex domain of Notch, BMC Developmental Biology, 8 : 4.
Baker, N.E. and Li, W. (2008)  Cell competition and its possible relation to cancer.  Cancer Research 68 , 5505-5507.
Bhattacharya, A. and Baker, N.E. (2009)  The HLH protein Extramacrochaetae is required for R7 and cone cell fates in the Drosophila eye Dev. Biol. 327 , 288-300.
Firth, L.C. and Baker (2009)  Retinal determination genes as targets and possible effectors of extracellular signals. Dev. Biol. 327 , 366-375.
Fullard, J.F., Kale, A., and Baker, N.E.   (2009).  Clearance of apoptotic corpses.  Apoptosis , 14 , 1029-1037.
Baker, N.E., Bhattacharya, A., and Firth, L.C. (2009) Regulation of Hedgehog signal transduction as Drosophila eye differentiation progresses.  Developmental Biology , 335 , 356-366.
Li, W., Kale, A., and Baker, N.E.   (2009) Oriented cell division as a response to cell death and cell competition.  Current Biology , 19 1821-1826.

 

http://fruitfly4.aecom.yu.edu/index.html

  • 0
    点赞
  • 0
    收藏
    觉得还不错? 一键收藏
  • 0
    评论
翻译The complex 3D geometries of these submillimeter-scale robots originate from planar (2D) multilayer assemblies formed with deposition and patterning techniques used in the semiconductor industry. Figure 1 (A and B) illustrates the process of transformation that converts these 2D precursors into 3D shapes for the case of a design inspired by the geometry of a peekytoe crab (Cancer irroratus) but engineered to a much smaller dimensions (~1/150 of the actual size; fig. S1). The precursors incorporate layers of SMA (nitinol; 2.5 m in thickness) as a collection of dynamic mechanical joints for locomotion, a film of polyimide (PI; ~8 m in thickness) as a static skeleton for structural support, and pads of silicon dioxide (SiO2; 100 nm in thickness) as bonding sites in the 2D to 3D transformation process (left frames in Fig. 1, A and B). This process begins with transfer printing to deliver these 2D precursors onto the surface of a prestretched silicone elastomer (Dragon Skin 10 Slow, ~500 m in thickness) that supports structures of polydimethylsiloxane (PDMS; blocks) located near the claws and back legs (middle frame in Fig. 1B). Releasing the prestrain imposes compressive stresses at the bonding sites, with forces sufficient to convert the 2D structures into 3D architectures via a set of controlled bending/ twisting deformations and translational/rotational motions (31, 32). During this process, the distance between the two PDMS blocks also decreases, thereby deforming the claws and back legs. This transformation involves peak strains (<4%) that lie below the maximum phase transition strain of the SMA (right frame in Fig. 1B).
06-12

“相关推荐”对你有帮助么?

  • 非常没帮助
  • 没帮助
  • 一般
  • 有帮助
  • 非常有帮助
提交
评论
添加红包

请填写红包祝福语或标题

红包个数最小为10个

红包金额最低5元

当前余额3.43前往充值 >
需支付:10.00
成就一亿技术人!
领取后你会自动成为博主和红包主的粉丝 规则
hope_wisdom
发出的红包
实付
使用余额支付
点击重新获取
扫码支付
钱包余额 0

抵扣说明:

1.余额是钱包充值的虚拟货币,按照1:1的比例进行支付金额的抵扣。
2.余额无法直接购买下载,可以购买VIP、付费专栏及课程。

余额充值