Toxicity of semaphorin3A for dopaminergic neurons

Takao Yasuhara, Tetsuro Shingo, Kenichiro Muraoka, Masahiro Kameda, Takashi Agari, Yuan Wenji, Tomohito Hishikawa, Toshihiro Matsui, Yasuyuki Miyoshi, Toru Kimura, Cesario V. Borlongan, Isao Date

Research output: Contribution to journalArticle

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Abstract

Semaphorin3A (Sema3A) is known to cause neuronal apoptosis and serves as a chemorepellent factor for axonal growth. In our previous report, we found that Sema3A was up-regulated in the 6-OHDA-injected striatum of rats, suggesting that Sema3A was likely involved in dopaminergic (DA) depletion. In this study, we investigated whether Sema3A directly worked as a neurotoxin to DA neurons both in vitro and in vivo. First, effects of various dosages of Sema3A administration on the DA neurons of the E14 murine ventral mesencephalon were examined in vitro. Sema3A at a dose over 500 ng/ml induced apoptosis to DA neurons. Next, we examined whether the continuous infusion of Sema3A exerted degeneration of DA neurons in rats. We established a Sema3A-secreting cell line (BHK-Sema3A), confirming the secreting functions by immunocytochemical and Western blot assays. Adult Sprague-Dawley rats were unilaterally implanted into the striatum with BHK-Sema3A or BHK non-Sema3A control cells, and subsequently underwent behavioral and immunohistochemical evaluations. Rats that received BHK-Sema3A did not show significant differences in the number of amphetamine- and apomorphine-induced rotations and TH-positive neurons in the substantia nigra pars compacta compared to the control group. Our results revealed that Sema3A was toxic to cultured DA neurons at very high dosages, but the continuous secretion of Sema3A at modest dosage in vivo did not produce Parkinsonian pathophysiologic symptoms. Optimizing the dosage and infusion location (i.e., nigra) and timing (more than 1 week post-transplantation) might further reveal the contribution of Sema3A to the pathogenesis of Parkinson's disease.

Original languageEnglish
Pages (from-to)61-65
Number of pages5
JournalNeuroscience Letters
Volume382
Issue number1-2
DOIs
Publication statusPublished - Jul 1 2005

Fingerprint

Dopaminergic Neurons
Apoptosis
Apomorphine
Poisons
Oxidopamine
Neurotoxins
Amphetamine
Mesencephalon
Sprague Dawley Rats
Parkinson Disease
Intercellular Signaling Peptides and Proteins
Transplantation
Western Blotting
Neurons
Cell Line
Control Groups
In Vitro Techniques

Keywords

  • Cell transplantation
  • Neurotoxicity
  • Parkinson's disease
  • Rat
  • Semaphorin3A
  • VEGF

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Toxicity of semaphorin3A for dopaminergic neurons. / Yasuhara, Takao; Shingo, Tetsuro; Muraoka, Kenichiro; Kameda, Masahiro; Agari, Takashi; Wenji, Yuan; Hishikawa, Tomohito; Matsui, Toshihiro; Miyoshi, Yasuyuki; Kimura, Toru; Borlongan, Cesario V.; Date, Isao.

In: Neuroscience Letters, Vol. 382, No. 1-2, 01.07.2005, p. 61-65.

Research output: Contribution to journalArticle

Yasuhara, T, Shingo, T, Muraoka, K, Kameda, M, Agari, T, Wenji, Y, Hishikawa, T, Matsui, T, Miyoshi, Y, Kimura, T, Borlongan, CV & Date, I 2005, 'Toxicity of semaphorin3A for dopaminergic neurons', Neuroscience Letters, vol. 382, no. 1-2, pp. 61-65. https://doi.org/10.1016/j.neulet.2005.02.064
Yasuhara, Takao ; Shingo, Tetsuro ; Muraoka, Kenichiro ; Kameda, Masahiro ; Agari, Takashi ; Wenji, Yuan ; Hishikawa, Tomohito ; Matsui, Toshihiro ; Miyoshi, Yasuyuki ; Kimura, Toru ; Borlongan, Cesario V. ; Date, Isao. / Toxicity of semaphorin3A for dopaminergic neurons. In: Neuroscience Letters. 2005 ; Vol. 382, No. 1-2. pp. 61-65.
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