Darcie L. Moore

Position title: Assistant Professor || PhD - Neuroscience, University of Miami, Florida || Post-doc - ETH Zürich/University of Zürich, Switzerland

Email: darcie.moore@wisc.edu

Phone: Phone: (608) 265-7836 | Fax: (608)265-5512

RESEARCH INTERESTS - Neural stem cells and aging

Darcie Moore

Moore Lab Website

Positions available:
Graduate students
Postdoctoral fellows

We are a lab that gets excited about science.

If you do too, please contact Dr. Moore for more information on specific projects.

Throughout life, stem cells are responsible for replenishing and regenerating tissue, fundamentally maintaining “youthfulness.” However, with aging, this ability is decreased, resulting in effects such as cognitive impairment, reduced immune response, deterioration of skeletal muscle, and difficulty in wound healing, for example. To develop methods to improve or rescue aging of somatic stem cells, we must understand not only how they age, but also how they remain young. Recently, we have shown that neural stem cells (NSCs) asymmetrically segregate cargoes (e.g. damaged proteins) when they divide, leaving one daughter cell more “clean” than the other. In addition, we have identified a diffusion barrier in the endoplasmic reticulum membrane in dividing NSCs that may limit the movement of these cargoes. Indeed, we have found that diffusion barrier strength weakens with age, correlating with a more symmetric distribution of aging factors, suggesting that this may be a mechanism for the segregation (Moore et al, 2015, Science).

In mammalian NSCs, the daughter cell which inherits the damage has a slower proliferation rate than the more “clean” daughter, suggesting that this process may be utilized by the cell as a method of cellular rejuvenation (Moore et al, 2015, Science). We hypothesize that stem cells use the asymmetric segregation of cargoes as a mechanism to remain “young,” and that loss of this asymmetry and the weakening of the diffusion barrier with age greatly contributes to the stem cell aging phenotype seen in the body.

The research in my lab focuses on identifying the mechanisms that stem cells use to create the asymmetric segregation of cargoes, to identify what other components are segregated, and to use this knowledge to improve stem cell aging. We use mammalian embryonic stem cells and adult neural stem cells as model systems in our research, with interest in broadening our somatic stem cell portfolio. We employ cell biology, biochemistry, molecular biology, genetics, and computational approaches to address our questions. Our lab specifically focuses on using advanced live imaging technologies, including FLIP, FRAP, photoactivation, 4D timelapse, and computer learning-based high-throughput imaging to interrogate cargoes in mitotic stem cells. If you can see it, you can believe it.

Moore - 1
(Above) A dividing embryonic neural stem cell overexpressing vimentin-eGFP (green) and a membrane marker (Kusabira orange) outlining the cell, demonstrates an asymmetric distribution of vimentin to the non-stem daughter cell. (Above) A mouse neural stem cell is seen in telophase in bright field. Shown in blue are the nuclei, and red are the ubiquitinated proteins. Note that the ubiquitinated proteins are asymmetrically segregated between the two daughter cells.

Recent Honors
2017  –  American Federation for Aging (AFAR) Research Grant for Junior Faculty
2017  –  Alfred P. Sloan Research Fellow in Neuroscience
2016  –  Society for Neuroscience Peter and Patricia Gruber International Research Award

Selected Publications

  • D.L. Moore*, S. Jessberger* (2017) Creating Age Asymmetry: Consequences of Inheriting Damaged Goods in Mammalian Neural Stem Cells. Trends in Cell Biology27(1): 82-92. *co-corresponding authors
  • D.L. Moore, G.A. Pilz, M.J. Arauzo-Bravo, Y. Barral, S. Jessberger (2015). A mechanism for the segregation of age in mammalian neural stem cells. Science, 349(6254): 1334-1338.
  • D.L. Moore, S. Jessberger. (2013). All astrocytes are not created equal – the role of astroglia in brain injury. EMBO Reports, 14(6): 487-8.
  • D.L. Moore, J.L. Goldberg (2011). Multiple transcription factor families regulate axon growth and regeneration. Developmental Neurobiology, 71(12): 1186-211
  • D.L. Moore, A. Apara, and J.L. Goldberg (2011). Kruppel-Like Transcription Factors in the Nervous System: Novel players in neurite outgrowth and axon regeneration. Molecular and Cellular Neuroscience, 47(4): 233-43.
  • D.L. Moore and J.L. Goldberg (2010). Four steps to optic nerve regeneration. J Neuro-ophthalmology, 30(4): 347-60.
  • M.G. Blackmore, D.L. Moore, R.P. Smith, J.L. Goldberg, J.L. Bixby, and V.P. Lemmon (2010). High content screening of cortical neurons identifies novel regulators of axon growth. Molecular and Cellular Neuroscience, 44(1): 43-54
  • D.L. Moore, M.G. Blackmore, Y. Hu, K.H. Kaestner, J.L. Bixby, V.P. Lemmon, and J.L. Goldberg (2009). KLF Family Members Regulate Intrinsic Axon Regeneration Ability. Science, 326(5950): 298-301.