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Der intrinsische apoptotische Weg
Interner zellulärer Stress, wie z. B. Zellschäden oder Hypoxie, löst intrinsische Apoptose aus. Die Proteinfamilie des B-Zell-Lymphoms 2 (Bcl-2) ist d…
Der intrinsische apoptotische Signalweg wird durch intrazelluläre Todessignale wie oxidativen Stress und DNA-Schäden aktiviert.
Bei Säugetieren wird der Signalweg durch die Bcl-2-Proteinfamilie reguliert, die sowohl pro- als auch anti-apoptotische Familienmitglieder hat.
Zu den proapoptotischen Proteinen gehören reine BH3-Proteine wie Bad und Bim sowie Proteine der Effektor-Bcl-2-Familie wie Bax und Bak. Zu den antiapoptotischen Proteinen gehören Bcl-X L und Bcl-2 und hemmen die Bax- und Bak-Aktivität.
Todessignale aktivieren die BH3-only-Proteine, die entweder anti-apoptotische Proteine inaktivieren oder direkt an Effektorproteine binden können.
In beiden Fällen oligomerisieren diese Effektoren an der Mitochondrienmembran und bilden Poren, die Cytochrom c freisetzen.
Cytochrom c bindet an apoptotische Protease-aktivierende Faktor-1-, Apaf-1- und Apaf-1-Monomere und baut sich dann zu einem heptameren Komplex zusammen, der als Apoptosom bezeichnet wird.
Als nächstes bindet der Initiator Procaspase-9 an das Apoptosom und dimerisiert unter Bildung von Caspase-9.
Schließlich aktiviert Caspase-9 die Henker-Caspasen, die zelluläre Proteine spalten, was zur Apoptose führt.
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Q1: What intracellular signals trigger the intrinsic apoptotic pathway?
The intrinsic apoptotic pathway is activated by intracellular death signals, including oxidative stress and DNA damage. When DNA damage occurs, checkpoint proteins like ATM and Chk2 are activated, which phosphorylate p53 and trigger pro-apoptotic responses. These internal cellular stressors, such as cellular injury or hypoxia, initiate the cascade leading to programmed cell death.
Q2: How do Bcl-2 family proteins regulate the intrinsic apoptotic pathway?
The Bcl-2 family contains both pro-apoptotic and anti-apoptotic members that balance cell survival and death. Pro-apoptotic proteins like Bax, Bak, and BH3-only proteins activate apoptosis, while anti-apoptotic proteins like Bcl-XL and Bcl-2 inhibit them. Death signals activate BH3-only proteins, which either inactivate anti-apoptotic proteins or directly bind effector proteins to initiate the pathway.
Q3: What happens when Bax and Bak proteins oligomerize on the mitochondrial membrane?
When Bax and Bak oligomerize on the mitochondrial membrane, they form pores that release cytochrome c into the cytoplasm. Cytochrome c then binds to Apaf-1, triggering assembly of a heptameric complex called the apoptosome. This structure recruits and activates procaspase-9, which becomes caspase-9 and initiates the executioner caspase cascade.
Q4: What is the role of the apoptosome in the intrinsic apoptotic pathway?
The apoptosome is a heptameric complex formed when cytochrome c binds to Apaf-1 monomers and they assemble together. This structure serves as a platform that recruits and activates the initiator procaspase-9, converting it to active caspase-9. Caspase-9 then activates executioner caspases that cleave cellular proteins, resulting in apoptosis.
Q5: How is the intrinsic apoptotic pathway disrupted in cancer cells?
Cancer cells often have mutations that inhibit the intrinsic apoptotic pathway. Overexpression of anti-apoptotic proteins like Bcl-2 prevents cell death, while inhibitor of apoptosis proteins (IAPs) inactivate caspase-9. These alterations allow damaged cells to survive when they should undergo apoptosis, contributing to tumor development and progression.
Q6: What anti-cancer drugs activate the intrinsic apoptotic pathway?
Several anti-cancer drugs have been developed to reactivate the intrinsic apoptotic pathway in cancer cells. Molecules like Nutlin-2 and MI-219 inhibit MDM2 binding to p53, preventing p53 inactivation and promoting apoptosis. Other drugs such as SH122, JP1201, and YM155 inhibit IAPs and activate caspases, initiating apoptosis in cancer cells.
Q7: How does p53 activation lead to apoptosis during DNA damage?
During DNA damage, checkpoint proteins ATM and Chk2 phosphorylate p53, activating it as a transcription factor. p53 then activates pro-apoptotic proteins such as Bax, Bak, PUMA, and Noxa while inhibiting anti-apoptotic proteins like Bcl-2 and Bcl-XL. This coordinated shift in Bcl-2 family protein balance triggers the mitochondrial pathway, leading to apoptosis of damaged cells.