Honors & Awards

  • The Helen Hay Whitney Fellowship Award, The Helen Hay Whitney Foundation (2016-2019)
  • The Paul Ehrlich Research Award, The Johns Hopkins University (April 17, 2014)
  • Chinese Government Award for Outstanding Students Abroad, China Scholarship Council (2013)

Professional Education

  • Bachelor of Science, Tsinghua University (2006)
  • Doctor of Philosophy, Johns Hopkins University (2014)

Stanford Advisors


All Publications

  • Glia Get Neurons in Shape. Cell Sun, L. O., Barres, B. A. 2016; 165 (4): 775-776


    Glial cells are essential components of the nervous system. In this issue, Singhvi et al. uncover cellular and molecular mechanisms through which C. elegans glia shape sensory neuron terminals and thus control animal thermosensing behaviors.

    View details for DOI 10.1016/j.cell.2016.04.052

    View details for PubMedID 27153490

  • Functional Assembly of Accessory Optic System Circuitry Critical for Compensatory Eye Movements. Neuron Sun, L. O., Brady, C. M., Cahill, H., Al-Khindi, T., Sakuta, H., Dhande, O. S., Noda, M., Huberman, A. D., Nathans, J., Kolodkin, A. L. 2015


    Accurate motion detection requires neural circuitry that compensates for global visual field motion. Select subtypes of retinal ganglion cells perceive image motion and connect to the accessory optic system (AOS) in the brain, which generates compensatory eye movements that stabilize images during slow visual field motion. Here, we show that the murine transmembrane semaphorin 6A (Sema6A) is expressed in a subset of On direction-selective ganglion cells (On DSGCs) and is required for retinorecipient axonal targeting to the medial terminal nucleus (MTN) of the AOS. Plexin A2 and A4, two Sema6A binding partners, are expressed in MTN cells, attract Sema6A(+) On DSGC axons, and mediate MTN targeting of Sema6A(+) RGC projections. Furthermore, Sema6A/Plexin-A2/A4 signaling is required for the functional output of the AOS. These data reveal molecular mechanisms underlying the assembly of AOS circuits critical for moving image perception.

    View details for DOI 10.1016/j.neuron.2015.03.064

    View details for PubMedID 25959730

  • Dlg5 Regulates Dendritic Spine Formation and Synaptogenesis by Controlling Subcellular N-Cadherin Localization JOURNAL OF NEUROSCIENCE Wang, S. J., Celic, I., Choi, S., Riccomagno, M., Wang, Q., Sun, L. O., Mitchell, S. P., Vasioukhin, V., Huganir, R. L., Kolodkin, A. L. 2014; 34 (38): 12745-12761
  • Cas Adaptor Proteins Organize the Retinal Ganglion Cell Layer Downstream of Integrin Signaling NEURON Riccomagno, M. M., Sun, L. O., Brady, C. M., Alexandropoulos, K., Seo, S., Kurokawa, M., Kolodkin, A. L. 2014; 81 (4): 779-786


    Stratification of retinal neuronal cell bodies and lamination of their processes provide a scaffold upon which neural circuits can be built. However, the molecular mechanisms that direct retinal ganglion cells (RGCs) to resolve into a single-cell retinal ganglion cell layer (GCL) are not well understood. The extracellular matrix protein laminin conveys spatial information that instructs the migration, process outgrowth, and reorganization of GCL cells. Here, we show that the ?1-Integrin laminin receptor is required for RGC positioning and reorganization into a single-cell GCL layer. ?1-Integrin signaling within migrating GCL cells requires Cas signaling-adaptor proteins, and in the absence of ?1-Integrin or Cas function retinal neurons form ectopic cell clusters beyond the inner-limiting membrane (ILM), phenocopying laminin mutants. These data reveal an essential role for Cas adaptor proteins in ?1-Integrin-mediated signaling events critical for the formation of the single-cell GCL in the mammalian retina.

    View details for DOI 10.1016/j.neuron.2014.01.036

    View details for Web of Science ID 000331464400009

    View details for PubMedID 24559672

  • On and Off Retinal Circuit Assembly by Divergent Molecular Mechanisms SCIENCE Sun, L. O., Jiang, Z., Rivlin-Etzion, M., Hand, R., Brady, C. M., Matsuoka, R. L., Yau, K., Feller, M. B., Kolodkin, A. L. 2013; 342 (6158): 590-?
  • Sema6B, Sema6C, and Sema6D Expression and Function during Mammalian Retinal Development PLOS ONE Matsuoka, R. L., Sun, L. O., Katayama, K., Yoshida, Y., Kolodkin, A. L. 2013; 8 (4)


    In the vertebrate retina, the formation of neural circuits within discrete laminae is critical for the establishment of retinal visual function. Precise formation of retinal circuits requires the coordinated actions of adhesive and repulsive molecules, including repulsive transmembrane semaphorins (Sema6A, Sema5A, and Sema5B). These semaphorins signal through different Plexin A (PlexA) receptors, thereby regulating distinct aspects of retinal circuit assembly. Here, we investigate the physiological roles of three Class 6 transmembrane semaphorins (Sema6B, Sema6C, and Sema6D), previously identified as PlexA receptor ligands in non-retinal tissues, in mammalian retinal development. We performed expression analysis and also phenotypic analyses of mice that carry null mutations in each of genes encoding these proteins using a broad range of inner and outer retinal markers. We find that these Class 6 semaphorins are uniquely expressed throughout postnatal retinal development in specific domains and cell types of the developing retina. However, we do not observe defects in stereotypical lamina-specific neurite stratification of retinal neuron subtypes in Sema6B-/- or Sema6C-/-; Sema6D-/- retinas. These findings indicate these Class 6 transmembrane semaphorins are unlikely to serve as major PlexA receptor ligands for the assembly of murine retinal circuit laminar organization.

    View details for DOI 10.1371/journal.pone.0063207

    View details for Web of Science ID 000319077300156

    View details for PubMedID 23646199

  • Guidance-Cue Control of Horizontal Cell Morphology, Lamination, and Synapse Formation in the Mammalian Outer Retina JOURNAL OF NEUROSCIENCE Matsuoka, R. L., Jiang, Z., Samuels, I. S., Nguyen-Ba-Charvet, K. T., Sun, L. O., Peachey, N. S., Chedotal, A., Yau, K., Kolodkin, A. L. 2012; 32 (20): 6859-6868


    In the vertebrate retina, neuronal circuitry required for visual perception is organized within specific laminae. Photoreceptors convey external visual information to bipolar and horizontal cells at triad ribbon synapses established within the outer plexiform layer (OPL), initiating retinal visual processing. However, the molecular mechanisms that organize these three classes of neuronal processes within the OPL, thereby ensuring appropriate ribbon synapse formation, remain largely unknown. Here we show that mice with null mutations in Sema6A or PlexinA4 (PlexA4) exhibit a pronounced defect in OPL stratification of horizontal cell axons without any apparent deficits in bipolar cell dendrite or photoreceptor axon targeting. Furthermore, these mutant horizontal cells exhibit aberrant dendritic arborization and reduced dendritic self-avoidance within the OPL. Ultrastructural analysis shows that the horizontal cell contribution to rod ribbon synapse formation in PlexA4?/? retinas is disrupted. These findings define molecular components required for outer retina lamination and ribbon synapse formation.

    View details for DOI 10.1523/JNEUROSCI.0267-12.2012

    View details for Web of Science ID 000304419700012

    View details for PubMedID 22593055

  • Receptor-like tyrosine phosphatase PTP10D is required for long-term memory in Drosophila JOURNAL OF NEUROSCIENCE Qian, M., Pan, G., Sun, L., Feng, C., Xie, Z., Tully, T., Zhong, Y. 2007; 27 (16): 4396-4402


    Tyrosine phosphorylation mediates multiple signal transduction pathways that play key roles in developmental processes and behavioral plasticity. The level of tyrosine phosphorylation is regulated by protein tyrosine kinases and protein tyrosine phosphatases (PTPs). Extensive studies have investigated the roles of tyrosine kinases in memory formation. However, there were few studies on PTPs. To date, learning has been shown to be defective only for mouse knock-outs of PTPalpha, leukocyte common antigen-related, or PTPdelta. A major limitation of these studies arises from their inability to distinguish an acute (biochemical) impairment of memory formation from a more chronic abnormality in neurodevelopment. From a behavioral screen for defective long-term memory, we found chi mutants to disrupt expression of the PTP10D protein tyrosine phosphatase gene. We show that chi mutants are normal for learning, early memory, and anesthesia-resistant memory, whereas long-term memory specifically is abolished. Significantly, induction of a heat shock-PTP10D+ transgene before training fully rescues the memory defect of chi mutants, thereby demonstrating an acute role for PTP10D in behavioral plasticity. We show that PTP10D is widely expressed in the embryonic CNS and in the adult brain. Transgenic expression of upstream activating sequence-PTP10D+ in mushroom bodies is sufficient to rescue the memory defect of chi mutants. Our data clearly demonstrate that signaling through PTP10D in mushroom bodies is critical for the formation of long-term memory.

    View details for DOI 10.1523/JNEUROSCI.4054-06.2007

    View details for Web of Science ID 000245810200019

    View details for PubMedID 17442824

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