Rachel Groth

Ph.D. 2006

Thesis Title:

NFAT-Dependent Transcription Within the Nervous System: A Critical Mediator of Neurotrophin-Induced Plasticity

Current Position:

Principle Scientist, Centers for Therapeutic Innovation, Pfizer

Undergraduate Institution and Major/Degree:

Macalester College, BA, Biology, Neuroscience, 2000

Major Advisor(s):

Research Description:

Gene expression activated by the neurotrophins nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) underlies such diverse processes as the refinement of neuronal connections during development, to learning and memory within the adult brain, to hyperalgesia following tissue injury and inflammation . To date, however, the mechanisms by which these neurotrophins induce gene expression are not fully understood. Recently, members of the NFATc family of transcription factors have also been implicated in shaping long-term changes in cellular functioning. Intriguingly, neurotrophin signaling appears ideally suited to activate NFATc transcription factors. As such, the experiments of my thesis project are designed to investigate the role of NFAT-dependent transcription in the neurotrophin-mediated gene expression required to establish enduring changes in synaptic neurotransmission. These experiments are organized to address the following three specific aims:  

  1. To determine whether NFAT-dependent transcription underlies BDNF-mediated activity-dependent synaptic plasticity within hippocampal neurons.
  2. To determine whether NFAT-dependent transcription underlies neurotrophin-mediated activity-dependent synaptic plasticity within DRG and spinal neurons.
  3. To determine whether neurotrophin-induced NFAT-dependent transcription underlies the development of hyperalgesia .

The proposed research will serve to further the understanding of:(1) the mechanisms by which neurotrophin signaling elicits lasting changes in cellular functioning, (2) the regulation of NFAT-dependent transcription within the nervous system, and (3) the mechanism underlying the establishment of hyperalgesia, with the ultimate goal of identifying novel therapeutic approaches, by examining the role of NFATc transcription factors in neurotrophin-mediated gene expression in vitro and in a model of persistent pain in vivo.

Lab Rotations:

  • Virginia Seybold
  • Don Simone
  • Paul Mermelstein

Courses Taken Beyond the Core Courses:

  • GCD 8121 Adv Mol Genetics
  • NSC 8221 Neurobiol Pain
  • NSC 5462 Neurosci Drug Abuse
  • NSC 8222 Cent Reg Auto Funct

Graduate Level Minor:

  • Supporting Program

Conferences Attended and Presentations:

Conferences Attended:

  • Society for Neuroscience annual meeting - (1999 - 2004)
  • Pain Interest Group Meeting (2000, 2003, 2005)

Committee Members:

  • Glenn Giesler (chair)
  • Paul Mermelstein
  • Virginia Seybold
  • Stan Thayer

Selected Publications:

  • Wheeler DG*, Groth RD*, Ma H*, Barrett CF, Owen SF, Safa P, Tsien RW. (2012) Ca(V)1 and Ca(V)2 channels engage distinct modes of Ca(2+) signaling to control CREB-dependent gene expression. Cell. 149(5):1112-24. *Equal Contribution.
  • Ma H, Groth RD, Wheeler DG, Barrett CF, Tsien RW. (2011) Excitation-transcription coupling in sympathetic neurons and the molecular mechanism of its initiation. Neurosci Res. 70(1):2-8.
  • Groth RD, Lindskog M, Thiagarajan TC, Li L, Tsien RW. (2011) Beta Ca2+/CaM-dependent kinase type II triggers upregulation of GluA1 to coordinate adaptation to synaptic inactivity in hippocampal neurons. Proc Natl Acad Sci U S A. 108(2):828-33.
  • Lindskog M, Li L, Groth RD, Poburko D, Thiagarajan TC, Han X, Tsien RW. (2010) Postsynaptic GluA1 enables acute retrograde enhancement of presynaptic function to coordinate adaptation to synaptic inactivity. Proc Natl Acad Sci U S A. 107(50)21806-811.
  • Wheeler DG, Barrett CF, Groth RD, Safa P, Tsien RW. (2008) CaMKII locally encodes L-type channel activity to signal to nuclear CREB in excitation-transcription coupling. J Cell Biol. 183(5):849-63.
  • Groth RD, Tsien RW. (2008) A role for retinoic acid in homeostatic plasticity. Neuron. 60(2):192-4.
  • Groth RD*, Weick JP*, Bradley KC, Luoma JI, Aravamudan B, Klug JR, Thomas MJ, Mermelstein PG. (2008) D1 dopamine receptor activation of NFAT-mediated striatal gene expression. Eur J Neurosci. 27(1):31-42. *Equal contribution.
  • Groth RD and Mermelstein PG. (2007) NFAT-Dependent Gene Expression in the Nervous System: A Critical Mediator of Neurotrophin-Induced Plasticity. In: Dudek S (Ed) Transcriptional Regulation by Neuronal Activity (188-209). New York, Springer.
  • Groth RD, Coicou LG, Seybold VS. (2006) Neurotrophin Activation of NFAT-Dependent Transcription Within Primary Afferent and Spinal Neurons Contributes to Expression of Pro-Nociceptive Genes. J Neurochem. 102(4)1162-74.

Awards and Honors:

Professional Memberships:

  • Society for Neuroscience

Home Town:

  • Littleton, Colorado
Rachel Groth