Neurogenetics, Development and Evolution





  Marcia G. Honig, Ph.D.

MARCIA G. HONIG, Ph.D.

Professor
Department of Anatomy and Neurobiology
The University of Tennessee College of Medicine

Address

The University of Tennessee Health Science Center
855 Monroe Avenue, Suite 515
Memphis, TN 38163
Tel: (901) 448-5998; Fax: (901) 448-7193;
Lab: 534 Johnson Building

Education

Ph.D. Institution: Yale University, Department of Biology
Postdoctoral: State University of New York at Stony Brook, Department of Neurobiology and Behavior; University of Michigan, Department of Biology

Research Interests

My laboratory investigates how axons choose the correct pathways to grow along during development. We use the chick embryo as a model system because its accessibility allows us to perform experimental manipulations at virtually any point during embryonic development. Our work focuses on sensory neurons innervating the hindlimb and has shown that sensory neurons whose axons project along different peripheral nerves are different from one another at very early stages, before they make specific pathfinding decisions. Further, sensory axons respond to specific cues on one another and in the environment as they extend into the limb and grow to their appropriate targets.

Our recent surgical manipulations have shown that the initial formation of a major cutaneous nerve in the embryonic chick limb requires the presence of the target ectoderm during a critical time period when those axons are about to diverge from the hindlimb plexus. We subsequently demonstrated that BMP4, which is expressed in a discrete region of the limb, promotes cutaneous nerve formation. Current work in the lab is primarily aimed at determining how BMP4 signals sensory axons (i.e. directly or indirectly), and elucidating the molecular mechanisms underlying BMP4 action. To do this, we are employing a loss of function approach, in which shRNA constructs are transfected into cells, subsequently leading to the downregulation of the protein(s) of interest, focusing initially on the major receptors for BMP4.

In addition to a variety of molecular biological techniques, work in the lab involves the use of multiple labeling approaches (retrograde labeling, immunofluorescence, in situ hybridization), in conjunction with confocal laser scanning microscopy.

Recent Publications

  • Honig MG, Camilli SJ, Surineni KM, Knight BK, Hardin HM. The contributions of BMP4, positive guidance cues, and repulsive molecules to cutaneous nerve formation in the chick hindlimb. Dev Biol. 2005 Jun 1;282(1):257-73. PMID: 15936345
  • Honig MG, Camilli SJ, Xue QS. Ectoderm removal prevents cutaneous nerve formation and perturbs sensory axon growth in the chick hindlimb. Dev Biol. 2004 Feb 1;266(1):27-42. PMID: 14729476
  • Honig MG, Camilli SJ, Xue QS. Effects of L1 blockade on sensory axon outgrowth and pathfinding in the chick hindlimb. Dev Biol. 2002 Mar 1;243(1):137-54. PMID: 11846483
  • Xue Y, Honig MG. Ultrastructural observations on the expression of axonin-1: implications for the fasciculation of sensory axons during axonal outgrowth into the chick hindlimb. J Comp Neurol. 1999 Jun 7;408(3):299-317. PMID: 10340508
  • Honig MG, Petersen GG, Rutishauser US, Camilli SJ. In vitro studies of growth cone behavior support a role for fasciculation mediated by cell adhesion molecules in sensory axon guidance during development. Dev Biol. 1998 Dec 15;204(2):317-26. PMID: 9882473
  • Honig MG, Frase PA, Camilli SJ. The spatial relationships among cutaneous, muscle sensory and motoneuron axons during development of the chick hindlimb. Development. 1998 Mar;125(6):995-1004. PMID: 9463346
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