September 10th BIOS E108. Mechanisms of cell death in neurodegenerative diseases. Part II -Apoptosis -Ubiquitin Proteasome pathway UPP -Proteostasis: Chaperones Autophagy and Lysosomal protein degradation -Aberrant Cell Cycle re-entry. APOPTOSIS.
Mechanisms of cell death in neurodegenerative diseases. Part II
-Ubiquitin Proteasome pathway UPP
Autophagy and Lysosomal protein degradation
-Aberrant Cell Cycle re-entry
Steps that lead to apoptosis:
1-Condensation of nuclear chromatin
2-Compaction of cytosolic organelles and blebbing on the cell surface
3-Decrease in cell volume (the cell shrinks)
4-Alteration of plasma membrane
Necrosis is characterized by membrane destruction and loss of electron density in the cytosol. Apoptotic features of nuclear fragmentation, but no substantial necrotic features, are observed in neurons treated with 25 pmol/cm2 ProTα
The Journal of Cell Biology, Vol. 176, No. 6, March 12, 2007 853–862
Apoptosis is of Greek origin meaning "falling off". The term is used in an analogy to the apparent suicide of leaves resulting in the very visible color changes associated with the Autumn/Fall and that eventually leads to the leaves falling from the trees. Similarly, cells go through a predetermined sequence of events resulting in death and removal from the body.
5-10. Scanning electron microscopy. Epithelial cells. Different stages. Flat cells (Fig. 5) undergo different forms of rounding, surface blebbing and cell retraction (6-9) preceding the typical apoptotic figure shown in (10).
These proteins initiate the process, and are released from the mitochondria following mitochondrial injury or dysfunction
Group II: Caspase 2, 3, 7 action of group II caspases on substrates determines:
-no cell repair
-no cell cycle progression
Group III: Caspase 6, 8, 9, 10 will activate caspases of group I and II, beginning a chain reaction that lead to programmed cell death
Mitochondrial apoptotic pathway. Death can be induced by the binding of ligands (such as FasL) to specific receptors (such as FAS) located at the cell surface. FAS contains a cytoplasmic death domain where FADD (Fas-associated death domain) can bind in presence of FasL, and recruit Pro-caspase 8 for subsequent activation in caspase 8. This induces caspase 3 activation. Caspase 3 cleaves I-CAD, the inhibitor of CAD (Caspase-activated DNase), which is released to enter the nucleus and cleaves DNA. In addition caspase 8 cleaves Bid protein, resulting in a truncated Bid (tBid) that, upon dimerisation of Bax or Bad, causes the release of cytochrome c from mitochondria. The mechanisms by which Bax leads to mitochondrial membrane permeabilisation and subsequent release of pro-apoptotic factors still remain unclear. It is proposed that Bax could interact with the permeability transition pore, or form channels by self-oligomerization. This leads to the mitochondrial release of cytochrome c and Smac/Diablo (Smac: second mitochondrial- derived activator of caspase; Diablo: direct IAP-binding protein with low pI), AIF (apoptosis inducing factor) and various procaspases. Bcl2 inhibits the release of cytochrome C and AIF in the cytoplasm and prevents the variation of the permeability transition pore. In the cytosol, cytochrome c binds to Apaf-1 (apoptosis- protease- activating factor). Both proteins form the apoptosome, which converts procaspase 9 in caspase 9. This results in activation of downstream effector caspases. Smac/DIABLO binds to IAP (Inhibitors of apoptosis) and prevent them from inhibition of the caspase 9 and caspase 3 activation. AIF has an indirect role in chromosome degradation as it activates endonuclease G, a DNase that moves from the mitochondria to the nucleus during apoptosis. Interestingly to note, the mtDNA is not fragmented during apoptosis.
These pathways work through the activation of cell surface death receptors, activated downstream of certain stimuli.
Fas/CD95 TNFaR1 (tumor necrosis factor a receptor 1)
The DD (Death Domain) of these receptor binds to adaptor proteins with death effector domain (FADD-Fas associated protein with death domain) forming a complex that contains also caspase 8.
Caspase 8 derives following activation of pro-caspase 8 either by caspases or other proteins.
This exogenous pathway is involved in Huntington’s diseases, stroke, Parkinson, but not in AD. However, caspase 8 is activated in cultured cell models, but in neurons this pathway is resistant to activation of death cell receptor. Thus it is still not clear how this pathway lead to neuronal death.
Starts from mitochondria dysfunction!!!
-In any event, cytochrome c forms complexes with the apoptosis protease activating factor APAF1, and procaspase 9.
the Ubiquitin Proteasomal Pathway UPP
It is the cellular “system” to eliminate proteins, degrading them into small peptides, aminoacids.
In this way, proteins tend NOT TO accumulate in the cell. After they have been synthesized and have exerted their activity in the cell, proteins have to be eliminated, since new proteins are soon newly synthesized. This pathway is to avoid accumulation of proteins.
Protein accumulation is a phenomenon common to all the neurodegenerative diseases: failure of the UPP is one of the reason why proteins accumulate and then tend to form aggregates. MOST IMPORTANTLY, all the intracellular and extracellular lesions characteristic of neurodegenerative diseases DO CONTAIN ALSO UBIQUITIN.
-Ubiquitin is a small protein that occurs in most eukaryotic cells. Its main function is to mark other proteins for destruction, known as proteolysis.
-Several ubiquitin molecules attach to the condemned protein (polyubiquitination), and it then moves to a proteasome, a barrel-shaped structure where the proteolysis occurs. Ubiquitin can also mark transmembrane proteins (for example, receptors) for removal from the membrane.
-Ubiquitin consists of 76 amino acids. It is highly conserved among eukaryotic species: Human and yeast ubiquitin share 96% sequence identity.
The process of marking a protein with ubiquitin consists of a series of steps:
-Activation of ubiquitin by binding to an ubiquitin-activating enzyme E1.
-Transfer of ubiquitin from E1 to the ubiquitin-conjugating enzyme E2 via trans(thio)esterification.
-Then, the final transfer of ubiquitin to the target protein can occur either:
1- directly from E2. This is primarily used when ubiquitin is transferred to another ubiquitin already in place, creating a branched ubiquitin chain, or
2-via an E3 enzyme, which binds specifically to both E2 and the target protein. The target protein is usually a damaged or non-functional protein that is recognized by a destruction-targeting sequence. Ubiquitins then bind to a lysine residue in the target protein, eventually forming a tail of ubiquitin molecules. This is the typical way to mark specific proteins for proteolysis.
Finally, the marked protein is digested in the 26S-proteasome into small peptides, amino acids (usually 6-7 aa subunits). Although the ubiquitins also enter the proteasome, they are not degraded and may be used again.
Proteostasis: regulation of the homeostasis of proteins during the life span of a cell
Homeostasis: the property of a system that regulates its internal environment and tends to maintain a stable, constant condition.
Proteostasis: “refers to controlling the concentration, conformation, binding interaction, and location of individual proteins, by re-adapting the innate biology of the cell, often through transcriptional and translational mechanisms”.
The competition between cellular protein folding and degradation.
It has a crucial role maintaining a correct proteostasis.
Crucial role of quality control during aging
The Ubiquitin Proteasome Pathway
The Lysosomal Pathway
proteins, organelles, structure and aggregates
through the lysosomal pathway
Macroautophagy: a system to degrade entire regions of the cytosol, including organelles. First organelles are included into de novo formed double layers membranes, which are then sequestered and targeted to the lysosomes.
Very important in neurodegeneration as it destroys dysfunctional organelles such as mitochondria. It also target for degradation large aggregates that might disrupt the functionality of the cell
mTOR kinase involved in the regulation of this autophagic mechanism.
CMA or Chaperone Mediated Authophagy: a type of selective autophagy aimed at removing from the system selected proteins. Relation to this kind of autophagy and degradation of misfolded proteins.
Microautophagy: so far poorly characterized in mammals.
in the regulation of Autophagy
of a correct proteostasis
-Inhibiting formation of larger aggregates
-Favoring protein degradation/Autophagy
-Regulating the Insulin Signaling Pathway
“An older person who is responsible for young people on social occasions”
“To go somewhere with someone as his/her chaperone”
Proteins that help control protein homeostasis in any given time of the life of the cell
1-To recognize nascent polypeptides
2-During translation they contribute to
a) maturation of folding intermediates
b) assembly into multimeric complexes
c) transport to organelles
Chaperones regulate the formation of aggregates deposit in a model of “HD” worm:
age and client protein factors
on chaperones’ activity and aggregates formation
Htt and paramyosin aggregates
Current Opinion in Structural Biology 2010, 20:23–32
role of chaperones
Neuronal aberrant cell cycle re-entry
G0= resting or quiescent phase; G1=first gap phase; S= DNA replication phase; G2= second gap phase; M=mitosis.
-NGF deprivation: death with increased cell cycle markers
-Drugs that block cell cycle prevents NGF-deprivation related cell death
-Expression of cell cycle proteins increase
*in brain of neurodegenerative diseases (AD)
*in vulnerable neurons
Cell cycle re-entry: a permissive event to neurons vulnerability
The two hit hypothesis
Neurons must hold cell cycle in check!!
What if this fails?
in mature or immature neurons
renders neuron vulnerable to a second toxic insult
Expert Rev Mol Med. 2010 Jun 29;12:e19. Review.