Render Target: STATIC
Render Timestamp:
3/28/2025, 6:31:59 AM EDT
3/28/2025, 10:31:59 AM UTC
Commit: 461ca8d8fe5b1efd4c01fc87e5b5eb592e2d154a
Cell Signaling Technology Logo
1% for the planet logo

Regulation of Apoptosis

Access the full library of downloadable pathway diagrams, along with recommended products for each signaling pathway.

Casp-8,-10 Casp-12 Casp-9 Casp-2 Casp-3,-6,-7 Casp-9 NIK RIP RIP TRAF2 TAK1 ASK1 BID NF-κB NF-κB NF-κB IκBα IκBα IKKγ IKKβ IKKα FoxO1 FoxO1 p53 p53 p53 p53 c-Jun HtrA2 SirT2 XIAP Arts 14-3-3 APP DFF40 DFF45 Smac/ Diablo Cyto c Apaf-1 AIF HECTH9 Mcl-1 Endo G AIF Endo G Bcl-2 Bcl-xL tBID Bax Bak Bad p90RSK cdc2 ROCK ATM/ATR Chk1/2 JNK TNF, FasL, TRAIL TNF, FasL, TRAIL PIDD RAIDD Puma Noxa Bim PKC Erk1/2 PI3K Akt JNK JNK FADD TRADD RIP1 RIP FADD TRADD c-IAP c-IAP TRAF2 TRAF2 TRADD FADD Itch CYLD FLIP Calpain DFF40 LaminA/C ER Stress Trophic Factors DNA Fragmentation DNA Damage • Cell shrinking• Membrane blebbing Cytoplasm Cytoplasm Nucleus Cell Cycle Cellular Stress [Ca 2+ ] FLIPXIAP Bim PumaNoxa PARP rev. 01/14/20 Regulation of Apoptosis

2025 © Cell Signaling Technology. All Rights Reserved.

Apoptosis is a regulated cellular suicide mechanism characterized by nuclear condensation, cell shrinkage, membrane blebbing, and DNA fragmentation. Caspases, a family of cysteine proteases, are the central regulators of apoptosis. Initiator caspases (including caspase-2, -8, -9, -10, -11, and -12) are closely coupled to pro-apoptotic signals. Once activated, these caspases cleave and activate downstream effector caspases (including caspase-3, -6, and -7), which in turn execute apoptosis by cleaving cellular proteins following specific Asp residues. Activation of Fas and TNFR by FasL and TNF, respectively, leads to the activation of caspase-8 and -10. DNA damage induces the expression of PIDD, which binds to RAIDD and caspase-2 and leads to the activation of caspase-2. Cytochrome c released from damaged mitochondria is coupled to the activation of caspase-9. XIAP inhibits caspase-3, -7, and -9. Mitochondria release multiple pro-apoptotic molecules, such as Smac/Diablo, AIF, HtrA2, and Endo G, in addition to cytochrome c. Smac/Diablo binds to XIAP, preventing it from inhibiting caspases. Caspase-11 is induced and activated by pathological pro-inflammatory and pro-apoptotic stimuli and leads to the activation of caspase-1, thereby promoting inflammatory response and apoptosis by directly processing caspase-3. Caspase-12 and caspase-7 are activated under ER stress conditions. Anti-apoptotic ligands, including growth factors and cytokines, activate Akt and p90RSK. Akt inhibits Bad by direct phosphorylation and prevents the expression of Bim by phosphorylating and inhibiting the Forkhead family of transcription factors (FoxO). FoxO promotes apoptosis by upregulating pro-apoptotic molecules such as FasL and Bim.

Selected Reviews:

We would like to thank Prof. Junying Yuan, Harvard Medical School, Boston, MA, for reviewing this diagram.

created September 2008

revised November 2012