Alpha particles induce apoptosis through the sphingomyelin pathway

Jonathan H. Seideman, Branka Stancevic, Jimmy A. Rotolo, Michael R. McDevitt, Roger Howell, Richard N. Kolesnick, David A. Scheinberg

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

The sphingomyelin pathway involves the enzymatic cleavage of sphingomyelin to produce ceramide, a second messenger that serves as a key mediator in the rapid apoptotic response to various cell stressors. Low-linear energy transfer (LET) γ radiation can initiate this pathway, independent of DNA damage, via the cell membrane. Whether short-ranged, high-LET α particles, which are of interest as potent environmental carcinogens, radiotherapies and potential components of dirty bombs, can act through this mechanism to signal apoptosis is unknown. Here we show that irradiation of Jurkat cells with α particles emitted by the 225Ac-DOTA-anti-CD3 IgG antibody construct results in dose-dependent apoptosis. This apoptosis was significantly reduced by pretreating cells with cholesterol-depleting nystatin, a reagent known to inhibit ceramide signaling by interfering with membrane raft coalescence and ceramide-rich platform generation. The effects of nystatin on α-particle-induced apoptosis were related to disruption of the ceramide pathway and not to microdosimetry alterations, because similar results were obtained after external irradiation of the cells with a broad beam of collimated α particles using a planar 241Am source. External irradiation allowed for more precise control of the dosimetry and geometry of the irradiation, independent of antibody binding or cell internalization kinetics. Mechanistically consistent with these findings, Jurkat cells rapidly increased membrane concentrations of ceramide after external irradiation with an average of five α-particle traversals per cell. These data indicate that α particles can activate the sphingomyelin pathway to induce apoptosis.

Original languageEnglish (US)
Pages (from-to)434-446
Number of pages13
JournalRadiation Research
Volume176
Issue number4
DOIs
StatePublished - Oct 1 2011

Fingerprint

Alpha Particles
Sphingomyelins
Ceramides
apoptosis
alpha particles
Apoptosis
Linear Energy Transfer
Nystatin
cells
Jurkat Cells
irradiation
linear energy transfer (LET)
antibodies
Environmental Carcinogens
Nuclear Weapons
Membranes
Antibodies
Second Messenger Systems
carcinogens
membranes

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Radiation
  • Radiology Nuclear Medicine and imaging

Cite this

Seideman, J. H., Stancevic, B., Rotolo, J. A., McDevitt, M. R., Howell, R., Kolesnick, R. N., & Scheinberg, D. A. (2011). Alpha particles induce apoptosis through the sphingomyelin pathway. Radiation Research, 176(4), 434-446. https://doi.org/10.1667/RR2472.1
Seideman, Jonathan H. ; Stancevic, Branka ; Rotolo, Jimmy A. ; McDevitt, Michael R. ; Howell, Roger ; Kolesnick, Richard N. ; Scheinberg, David A. / Alpha particles induce apoptosis through the sphingomyelin pathway. In: Radiation Research. 2011 ; Vol. 176, No. 4. pp. 434-446.
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Seideman, JH, Stancevic, B, Rotolo, JA, McDevitt, MR, Howell, R, Kolesnick, RN & Scheinberg, DA 2011, 'Alpha particles induce apoptosis through the sphingomyelin pathway', Radiation Research, vol. 176, no. 4, pp. 434-446. https://doi.org/10.1667/RR2472.1

Alpha particles induce apoptosis through the sphingomyelin pathway. / Seideman, Jonathan H.; Stancevic, Branka; Rotolo, Jimmy A.; McDevitt, Michael R.; Howell, Roger; Kolesnick, Richard N.; Scheinberg, David A.

In: Radiation Research, Vol. 176, No. 4, 01.10.2011, p. 434-446.

Research output: Contribution to journalArticle

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AU - Seideman, Jonathan H.

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Seideman JH, Stancevic B, Rotolo JA, McDevitt MR, Howell R, Kolesnick RN et al. Alpha particles induce apoptosis through the sphingomyelin pathway. Radiation Research. 2011 Oct 1;176(4):434-446. https://doi.org/10.1667/RR2472.1