4.7 Article

Soluble adenylyl cyclase is required for netrin-1 signaling in nerve growth cones

Journal

NATURE NEUROSCIENCE
Volume 9, Issue 10, Pages 1257-1264

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nn1767

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Funding

  1. NCI NIH HHS [T32 CA062948, 5T32CA062948] Funding Source: Medline
  2. NICHD NIH HHS [HD38722, R01 HD038722, HD42060] Funding Source: Medline
  3. NIDA NIH HHS [T32 DA007274, 2T32 DA07274] Funding Source: Medline
  4. NIGMS NIH HHS [T32 GM007739, GM62328, GM07739, R01 GM062328] Funding Source: Medline
  5. NIMH NIH HHS [R01 MH066204, R01 MH066204-04, MH066204] Funding Source: Medline
  6. NINDS NIH HHS [R01 NS055255, R01 NS055255-01A1] Funding Source: Medline

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Growth cones at the tips of nascent and regenerating axons direct axon elongation. Netrin-1, a secreted molecule that promotes axon outgrowth and regulates axon pathfinding, elevates cyclic AMP (cAMP) levels in growth cones and regulates growth cone morphology and axonal outgrowth. These morphological effects depend on the intracellular levels of cAMP. However, the specific pathways that regulate cAMP levels in response to netrin-1 signaling are unclear. Here we show that 'soluble' adenylyl cyclase (sAC), an atypical calcium- regulated cAMP-generating enzyme previously implicated in sperm maturation, is expressed in developing rat axons and generates cAMP in response to netrin-1. Overexpression of sAC results in axonal outgrowth and growth cone elaboration, whereas inhibition of sAC blocks netrin-1-induced axon outgrowth and growth cone elaboration. Taken together, these results indicate that netrin-1 signals through sAC-generated cAMP, and identify a fundamental role for sAC in axonal development.

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