RIP1-dependent Bid cleavage mediates TNFα-induced but Caspase-3-independent cell death in L929 fibroblastoma cells.

L929 fibroblastoma cells (L929-A) and L929 fibrosarcoma cells (L929-N) are different cell lines that are commonly used to study the cytotoxicity of tumor necrosis factor alpha (TNFα). TNFα has been reported to induce necrosis in both of these cell lines. However, comparing the TNFα-induced cell death in these two cell lines, we found that, unlike the L929-N cells that show typical RIP3-dependent necrosis, TNFα-induced cell death in L929-A cells is pan-caspase inhibitor Z-VAD-FMK (Z-VAD)-sensitive, which does not depend on RIP3. We also confirmed that the cell death signal in the L929-A cells was initiated through cytosol-preassembled ripoptosome and that the knockdown of either Caspase-8 or RIP1 protein blocked cell death. Compared with the L929-N cells, the L929-A cell line had lower levels of constitutive and inducible TNFα autocrine production, and the pan-caspase inhibitors Z-VAD or Q-VD did not kill the L929-A cells as they affect the L929-N cells. Moreover, the L929-A cells expressed less RIP3 protein than the L929-N cells; therefore, TNFα failed to induce RIP3-dependent necroptosis. In addition, the ripoptosome-mediated cell death signal was transduced to the mitochondria through Caspase-8-mediated and RIP1 kinase activity-dependent Bid cleavage. The RIP1 kinase inhibitor Necrostatin-1 (Nec-1) or Caspase-8 knockdown completely blocked Bid cleavage, and the knockdown of Bid or Bax/Bak prevented TNFα-induced cell death in the L929-A cells. Although the activation of Bax/Bak decreased the mitochondrial membrane potential, the levels of mitochondrial intermembrane space proteins, including cytochrome-c (cyt-C) and Smac, declined, and western blotting and immunofluorescence staining analysis did not determine whether these proteins were redistributed to the cytosol. In addition, the mitochondrial outer membrane protein Tom20 was also reduced, indicating that the reduced mitochondria proteins may be induced by the reduced mitochondria numbers. No efficient cyt-C release was observed; therefore, the limited activation and cleavage of downstream caspases, including Caspase-9, Caspase-7, Caspase-6 and Caspase-3, was insufficient to kill the cells. The Caspase-9, Caspase-6 and Caspase-3/7 inhibitors or Caspase-9 and -3 knockdown also failed to block cell death, and the overexpression of Bcl-2 also did not abrogate cell death. Moreover, the dead cells showed necrotic-like but not apoptotic characteristics under transmission electronmicroscopy, and these features were significantly different from mitochondrial apoptosis, indicating that the effector caspases were not the executioners of cell death. These new discoveries show that TNFα-induced cell death in L929-A cells is different than typical RIP3-dependent necrosis and Caspase-8/Caspase-3-mediated apoptosis. These results highlight that caution is necessary when using different L929 cells as a model to investigate TNFα-induced cell death.
AuthorsGuozhu Chen, Xiang Cheng, Ming Zhao, Song Lin, Jiangyang Lu, Jiarui Kang, Xiaodan Yu
JournalApoptosis : an international journal on programmed cell death (Apoptosis) Vol. 20 Issue 1 Pg. 92-109 (Jan 2015) ISSN: 1573-675X [Electronic] Netherlands
PMID25398540 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Amino Acid Chloromethyl Ketones
  • BH3 Interacting Domain Death Agonist Protein
  • Bid protein, mouse
  • Caspase Inhibitors
  • GTPase-Activating Proteins
  • Ralbp1 protein, mouse
  • Tumor Necrosis Factor-alpha
  • benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone
  • Ripk3 protein, mouse
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Caspase 3
  • Caspase 8
  • Amino Acid Chloromethyl Ketones (pharmacology)
  • Animals
  • BH3 Interacting Domain Death Agonist Protein (chemistry, metabolism)
  • Caspase 3 (metabolism)
  • Caspase 8 (metabolism)
  • Caspase Inhibitors (pharmacology)
  • Cell Death (drug effects)
  • Cell Line, Tumor
  • Dermatofibrosarcoma (metabolism, pathology)
  • GTPase-Activating Proteins (metabolism)
  • Mice
  • Mitochondria (metabolism)
  • Receptor-Interacting Protein Serine-Threonine Kinases (metabolism)
  • Skin Neoplasms (metabolism, pathology)
  • Tumor Necrosis Factor-alpha (metabolism)

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