| Literature DB >> 12835323 |
Hong Liu1, Rachelle E Toman, Sravan K Goparaju, Michael Maceyka, Victor E Nava, Heidi Sankala, Shawn G Payne, Meryem Bektas, Isao Ishii, Jerold Chun, Sheldon Milstien, Sarah Spiegel.
Abstract
There are two isoforms of sphingosine kinase (SphK) that catalyze the formation of sphingosine 1-phosphate, a potent sphingolipid mediator. Whereas SphK1 stimulates growth and survival, here we show that SphK2 enhanced apoptosis in diverse cell types and also suppressed cellular proliferation. Apoptosis was preceded by cytochrome c release and activation of caspase-3. SphK2-induced apoptosis was independent of activation of sphingosine 1-phosphate receptors. Sequence analysis revealed that SphK2 contains a 9-amino acid motif similar to that present in BH3-only proteins, a pro-apoptotic subgroup of the Bcl-2 family. As with other BH3-only proteins, co-immunoprecipitation demonstrated that SphK2 interacted with Bcl-xL. Moreover, site-directed mutation of Leu-219, the conserved leucine residue present in all BH3 domains, markedly suppressed SphK2-induced apoptosis. Hence, the apoptotic effect of SphK2 might be because of its putative BH3 domain.Entities:
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Year: 2003 PMID: 12835323 DOI: 10.1074/jbc.M304455200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157