TY - JOUR
T1 - Sphingosine kinase type 2 is a putative BH3-only protein that induces apoptosis
AU - Liu, Hong
AU - Toman, Rachelle E.
AU - Goparaju, Sravan K.
AU - Maceyka, Michael
AU - Nava, Victor E.
AU - Sankala, Heidi
AU - Payner, Shawn G.
AU - Bektas, Meryem
AU - Ishii, Isao
AU - Chun, Jerold
AU - Milstien, Sheldon
AU - Spiegel, Sarah
PY - 2003/10/10
Y1 - 2003/10/10
N2 - 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 proapoptotic subgroup of the Bcl-2 family. As with other BH3-only proteins, co-immunoprecipitation demonstrated that SphK2 interacted with Bcl-x L. 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.
AB - 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 proapoptotic subgroup of the Bcl-2 family. As with other BH3-only proteins, co-immunoprecipitation demonstrated that SphK2 interacted with Bcl-x L. 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.
UR - http://www.scopus.com/inward/record.url?scp=0141924852&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0141924852&partnerID=8YFLogxK
U2 - 10.1074/jbc.M304455200
DO - 10.1074/jbc.M304455200
M3 - Article
C2 - 12835323
AN - SCOPUS:0141924852
SN - 0021-9258
VL - 278
SP - 40330
EP - 40336
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 41
ER -