Table of Contents

A Retrograde Neuronal Survival Response: Target-Derived Neurotrophins Regulate MEF2D and bcl-w

  1. Rosalind A. Segal1,2,3
  1. 1Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115,
  2. 2Departments of Cancer Biology and
  3. 3Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115,
  4. 4Department of Biology and Neuroscience Program, Washington and Lee University, Lexington, Virginia 24450, and
  5. 5Department of Neurobiology, Children's Hospital Boston and Harvard Medical School, Boston, Massachusetts 02115
  1. Correspondence should be addressed to Rosalind A. Segal, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115. Rosalind_segal{at}dfci.harvard.edu
  • A. Hans's present address: French Food Safety Agency, Laboratoire d'Etudes et de Recherches en Pathologie Equine, 14430 Dozulé, France.

  • C. Karch's present address: Newton, MA 02459.

  • H. M. Heerssen's present address: Helix Medical Communications, San Mateo, CA 94401.

  1. ↵*M.F.P.-M. and A.H. contributed equally to this work.

Abstract

Survival and maturation of dorsal root ganglia sensory neurons during development depend on target-derived neurotrophins. These target-derived signals must be transmitted across long distances to alter gene expression. Here, we address the possibility that long-range retrograde signals initiated by target-derived neurotrophins activate a specialized transcriptional program. The transcription factor MEF2D is expressed in sensory neurons; we show that expression of this factor is induced in response to target-derived neurotrophins that stimulate the distal axons. We demonstrate that MEF2D regulates expression of an anti-apoptotic bcl-2 family member, bcl-w. Expression of mef2d and bcl-w is stimulated in response to activation of a Trk-dependent ERK5/MEF2 pathway, and our data indicate that this pathway promotes sensory neuron survival. We find that mef2d and bcl-w are members of a larger set of retrograde response genes, which are preferentially induced by neurotrophin stimulation of distal axons. Thus, activation of an ERK5/MEF2D transcriptional program establishes and maintains the cellular constituents of functional sensory circuits.