We are interested in understanding the molecular basis of developmental plasticity. Current research is focused on medium spiny neurons (MSNs), the major type of neuron in the striatum. The striatum plays an important role in regulation of movement, motivation and reward and altered or abnormal activity of MSNs is associated with neurological diseases such as Huntington's (HD) and Parkinson's (PD) and is thought to be a major determinant of addiction. These changes in MSN activity have been correlated with changes in dendritic arborization and the number, distribution and morphology of dendritic spines. Current research in the lab uses a recently developed in vitro system are to 1) determine how neurotransmitter signaling affects MSN development and morphology, 2) analyze neurotransmitter receptor trafficking during dendritic spine development and 3) characterize the relationship between MSN development and network excitability. To achieve these goals, we use a combination of multi-electrode array (MEA) recordings and immunofluorescence microscopy to investigate the relationship between morphometric development and network activity of MSNs. Because it is easily amenable to molecular manipulation and microscopic visualization, future studies may use this in vitro model system to investigate the cellular and molecular mechanisms that regulate MSN development and function, determine the consequences of disease associated gene mutations and screen for drugs that regulate MSN synaptic properties.
(For a comprehensive list of recent publications, refer to PubMed, a service provided by the National Library of Medicine.)
- Bastian TW, von Hohenberg WC, Georgieff MK, Lanier LM. Chronic energy depletion due to iron deficiency impairs dendritic mitochondrial motility during hippocampal neuron development. J Neurosci. 2018 Dec 6. pii: 1504-18.
- Bastian TW, Duck KA, Michalopoulos GC, Chen MJ, Liu ZJ, Connor JR, Lanier LM, Sola-Visner MC, Georgieff MK. Eltrombopag, a thrombopoietin mimetic, crosses the blood-brain barrier and impairs iron-dependent hippocampal neuron dendrite development. J Thromb Haemost. 2017;15:565-574.
- Penrod RD, Campagna J, Panneck T, Preese L, Lanier LM. The presence of cortical neurons in striatal-cortical co-cultures alters the effects of dopamine and BDNF on medium spiny neuron dendritic development. Front Cell Neurosci. 2015 Jul 20;9:269.
- Penrod RD, Kourrich S, Kearney E, Thomas MJ, Lanier LM. An embryonic culture system for the investigation of striatal medium spiny neuron dendritic spine development and plasticity. J Neurosci Methods. 2011;200(1):1-13.
- Hoover BR, Reed MN, Su J, Penrod RD, Kotilinek LA, Grant MK, Pitstick R, Carlson GA, Lanier LM, Yuan LL, Ashe KH, Liao D. Tau mislocalization to dendritic spines mediates synaptic dysfunction independently of neurodegeneration. Neuron. 2010;68:1067-81.
- Xu X, Harder J, Flynn DC, Lanier LM. AFAP120 regulates actin organization during neuronal differentiation. Differentiation. 2009;77(1):38-47.
- Popko J, Fernandes A, Brites D, Lanier LM. Automated analysis of NeuronJ tracing data. Cytometry A. 2009;75(4):371-376.
- Fernandes A, Falcao AS, Abranches E, Bekman E, Henrique D, Lanier LM, et al. Bilirubin as a determinant for altered neurogenesis, neuritogenesis, and synaptogenesis. Dev Neurobiol. 2009;69:568-582.
- Harder J, Xu X, Letourneau P, Lanier LM. The actin cross-linking protein AFAP120 regulates axon elongation in a tyrosine phosphorylation-dependent manner. Neurosci Lett. 2008;444(2):132-136.
Former Graduate Students:
Marcela Maldonado (Ph.D. 2009, Neuroscience, University of Minnesota).
Rachel Penrod (Ph.D. 2012, Neuroscience, University of Minnesota).