Semaphorin 3A growth cone collapse requires a sequence homologous to tarantula hanatoxin
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Behar, O
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Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neural Plast Res Grp,Dept Anesthesia & Crit Care, Charlestown, MA 02129 USAHarvard Univ, Sch Med, Massachusetts Gen Hosp, Neural Plast Res Grp,Dept Anesthesia & Crit Care, Charlestown, MA 02129 USA
Behar, O
[1
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Mizuno, K
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机构:Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neural Plast Res Grp,Dept Anesthesia & Crit Care, Charlestown, MA 02129 USA
Mizuno, K
Badminton, M
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机构:Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neural Plast Res Grp,Dept Anesthesia & Crit Care, Charlestown, MA 02129 USA
Badminton, M
Woolf, CJ
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机构:Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neural Plast Res Grp,Dept Anesthesia & Crit Care, Charlestown, MA 02129 USA
Woolf, CJ
机构:
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Neural Plast Res Grp,Dept Anesthesia & Crit Care, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Div Cardiovasc, Charlestown, MA 02129 USA
[3] Univ London Univ Coll, Dept Anat & Dev Biol, London WC1E 6BT, England
Axonal guidance is key to the formation of neuronal circuitry. Semaphorin 3A (Sema 3A; previously known as semaphorin ill, semaphorin D, and collapsin-1), a secreted subtype of the semaphorin family, is an important axonal guidance molecule in vitro and in vivo. The molecular mechanisms of the repellent activity of semaphorins are, however, poorly understood. We have now found that the secreted semaphorins contain a short sequence of high homology to hanatoxin, a tarantula K+ and Ca2+ ion channel blocker. Point mutations in the hanatoxin-like sequence of Sema 3A reduce its capacity to repel embryonic dorsal root ganglion axons. Sema 3A growth cone collapse activity is inhibited by hanatoxin, general Ca2+ channel blockers, a reduction in extracellular or intracellular Ca2+, and a calmodulin inhibitor, but not by K+ channel blockers. Our data support an important role for Ca2+ in mediating the Sema 3A response and suggest that Sema 3A may produce its effects by causing the opening of Ca2+ channels.