Presentation on theme: "February 19 th BIOS E108 Parkinson’s disease: Parkin and PINK1 Mitochondrial fusion and fission, involved in PD? Toxic/Environmental factors that cause."— Presentation transcript:
February 19 th BIOS E108 Parkinson’s disease: Parkin and PINK1 Mitochondrial fusion and fission, involved in PD? Toxic/Environmental factors that cause PD Therapeutic approaches
Defective autophagy in PD: consequences on -synuclein
Loss of proteostasis causes loss of cellular homeostasis in PD
Are there proteins that disrupt cellular homeostasis in PD? Correct proteostasis guarantees a protein’s function to ultimately maintain cellular homeostasis Parkin and PINK1 as crucial regulator of Autophagy/Mitophagy. Loss of function and gain of toxic function in PD.
Parkin (PARK2) 1- Parkin is a protein-ubiquitin isopeptide ligase (E3), a component of the ubiquitin proteasome system that identifies substrates to drive them to the proteasomes for degradation (for review see Sherman and Goldberg, 2001) Parkin
2- Parkin it is ubiquitously expressed in the brain. Parkin-related PD is characterized by increased loss of dopaminergic neurons in the SNpc. 3- Mutations in Parkin cause a juvenile, autosomal recessive form of PD, with onset <30 years of age (ARJ-PD). 4- The gene for Parkin is expressed on chromosome 6. Parkin is a protein comprised of 465 aa, about 51.6 kDa. 5- Parkin is characterized by two RING finger domains rich in cysteins that confer the ubiquitin-ligase activity. RING1: aa RING2: aa Parkin is expressed i) in the nucleus, ii) associates to synaptic vesicles, and iii) within actin and - and -tubulin positive microfilaments. 7- Parkin is itself ubiquitinilated.
Parkin expression profile in human tissues (Kitada, 1998)
Physiological function of Parkin 1- Protects from neurotoxicity induced by unfolded protein stress: overexpression of Parkin suppresses the stress caused by unfolded protein. 2- Among Parkin substrates are: Cyclin E (expressed in different neuronal populations, accumulates in the brain of sporadic and parkin-mutated PD patients), Synphilin1 ( -synuclein interactin protein, expressed in different neuronal populations). 3- One of the most eminent substrates for Parkin is CDCrel-1, a member of the septins family, GTPases required for the regulation of cytokinesis in the cell. CDCrel-1 is expressed mostly in neurons, at synaptic vesicles, and its accumulation reduces the pool of released DA in dopaminergic neurons (reviewed in Mizuno, 2001). 4- Binds to actin and - and -tubulin positive microtubules, and stabilizes them. This interaction and activity are independent on the E3 ligase property of Parkin. In this respect it could be speculated that the role of Parkin in microtubules is not only to stabilize them but also to anchor E3 ligase to them, enabling microtubules to control the amount of proteins that need to be degraded through the proteasomal pathway (Yang 2005).
Genetic of Parkin 1- Point mutations in the RING1 domain change the intracellular localization of Parkin, redistributing it in aggregosomes (structures formed in response to misfolded proteins). 2- Mutated forms of Parkin co-localize with ubiquitin. 3-Spliced variants by deleted exons 3-7 and 4 are related to familial, juvenile PD. These data may suggest that: i) not all the mutations induce the same pathogenic mechanism; ii) some of these could be gain of toxic function more than loss of physiological function. The fact that mutant parkin still co-localizes with ubiquitin suggests that mutant parkin may still work as a E3 ligase, but the machine that leads to proteasomal degradation is somehow lost. (Cookson 2003)
Pathogenic mechanisms of Parkin Loss of physiological function 1- Loss of E3 ligase activity that leads to accumulation of parkin substrates (synphilin 1 and cyclin E which accumulate in Lewy bodies structures, and accumulate in the brain of PD patients). 2-Loss of E3 ligase activity on Mfn2: defective mitophagy (ubiquitinilation of Mfn2 precedes the removal of damaged mitochondria). 3- Lack of ubiquitinilation of CDCrel-1: this may cause accumulation of CDCrel-1 and reduce the amount of DA released. 4-Oxidative stress. 5-Covalent binding of Parkin to DA: changes in Parkin solubility, inactivation of Parkin E3 ligase activity (LeVoie, 2005). Gain of toxic function?
Facts: Parkin is a E3 ligase involved in familial PD. Parkin is rich in cysteine residues in the Ring domains, crucial for its activity as an E3 ligase. Question: Is Parkin able to bind covalently to oxidized dopamine forming insoluble Parkin species? If yes, is this process occurring in sporadic PD?
O2O2 + H 2 O 2 + O 2 - Oxidation of Dopamine and subsequent interaction with Cys residues on different substrates: first step to the formation of protofibrils tyrosinase
Oxidation of dopamine (DA quinone) directly fosters the transition of Parkin from soluble to insoluble non-reducing protein electrophoresis LaVoie et al., Nat Med Nov;11(11): E
Dopamine quinone inactivates Parkin E3 ligase activity LaVoie et al., Nat Med Nov;11(11): E
In PD patients, levels of insoluble Parkin increase SPECIFICALLY in the Caudate LaVoie et al., Nat Med Nov;11(11): E
Conclusions: 1-Parkin binds covalently to dopamine quinone in vitro and in vivo, changing its properties and becoming insoluble. This effect is observed specifically in the Caudate area in PD brain. 2-Binding to dopamine quinone causes loss of function, as Parkin loses its activity as E3 ligase. 3- Covalent binding of Parkin to dopamine quinone could be a potential pathogenic mechanism of neurodegeneration also in sporadic PD, by sequestering active soluble Parkin and fostering its transition to insoluble molecule. The formation of protofibrils could also occur.
PTEN-induced putative kinase protein 1, PINK1
Dark: identical sequences; Light: similar sequences; Green: MTS, Mitochondrial Targeting Sequence; Blue Brackets: Kinase domain; Red Boxes: Conserved aminoacids altered by missense mutations. PTEN-induced putative kinase protein 1, PINK1 Clark et al., 2006
PINK1 localizes to Mitochondria 1=total lysate 2=mitochondria enriched fraction
Expression of PINK1 in human brain areas
PINK1 co-localizes to Lewy Bodies in PD Sporadic PD PINK1 mutant PD
Park et al., 2006 PINK1 mutants have “downturned” wing phenotype
Clark et al., 2006 Muscle degeneration and mitochondrial cristae fragmentation is observed in adult PINK1 mutant flies…
Clark et al., 2006 …and is restored by re-expression of PINK1 in PINK1 mutants flies
PINK1 function may be crucial for maintaining mitochondrial integrity
Fibroblast of PD patients carrying mutations on PINK1 show altered mitochondrial morphology Category I swollen Category II truncated and swollen Category III fragmented Exner et al., J Neurosci Nov 7;27(45):
Overexpressd Parkin in PINK1 single mutant PINK1 and Parkin double mutant PINK1 single mutant Parkin rescues mitochondrial dysfunction in PINK1 mutants Clark et al., 2006
Commonalities between PINK1 and Parkin mutant 1-PINK1 knockout (mutant) phenotype resembles the phenotype observed in Parkin mutants flies (defective motor function). 2-PINK1 mutant flies have reduced ATP production, as a result of the mitochondrial dysfunction. 3-Dopaminergic degeneration is associated with structural mitochondrial abnormalities in PINK1 mutants. 4-In PINK1 mutants, muscle degeneration and mitochondrial fragmentation are associated with increased apoptosis. 5-Parkin rescues the phenotype caused by PINK1 mutant.
Parkin acts in the same pathway of PINK1
When working in the same pathway can PINK1 and Parkin regulate mitochondrial integrity? Is this pathway affected in PD?
Trends in Molecular Medicine, March 2011, Vol. 17, No. 3 pag 158 Hypotheses on the PINK1/parkin signaling pathway: a role in mitophagy
PINK1 and Parkin also to regulate mitochondrial trafficking and fission
Itoh et al., Trends in Cell Biology 2012 Mitochondrial dynamics in neurodegeneration Physiologic Fission and FusionBalance or disease
Cellular distribution of mitochondria in the neuron
Physiological role of mitochondrial fusion and fission Mitochondria exist as dynamic structures that keep changing their size. Physiologic fusion and division of mitochondria maintains a mitochondrial network. During apoptosis, mitochondria undergo fragmentation, preparing the cell to a lack of provided energy. This leads to a contained programmed cell death. Fusion and fission participate in apoptosis. Inhibiting the activity of proteins underlying these processes results in inhibition of apoptosis. Up-regulating the activity of these proteins may promote apoptosis.
Proteins involved in mitochondrial fusion and fission Fusion: dynamin-family members MFN1, MFN2 mitofusin 1 and 2, impairs mitochondrial fusion rate and shortens mitochondrial length. GTPase anchored to the outer membrane. N- and C-terminal domains face the cytosol, docking to each other and mediating docking of mitochondria to each other. Require GTP hydrolysis. OPA1 optic atrophy 1 protein (gene mutated in most forms of hereditary blindness). Large GTPase expressed in the intermembrane space, is anchored to the inner membrane. Loss of OPA1 expression leads to mitochondrial fragmentation, whereas ectopic OPA1 expression leads to mitochondrial fusion that does not require MFN2. Fusion occurs when both the inner and the outer mitochondrial membrane fuse: GTP hydrolysis necessary at both levels. Fission FIS1 binds to the outer membrane. The domain of the protein facing the cytosol binds cytosolic proteins involved in the fission, such as DRP1. DRP1 dynamin regulated protein 1, it’s a cytosolic protein recruited to the mitochondrial outer membrane by FIS1, visible as punctate foci at the site of mitochondrial division on the outer membrane. It forms a ring around the mitochondrion and mediates constriction of the organelle at that point.
Analysis of a possible role for PINK1 and Parkin in mitochondrial fusion and fission.
DRP1 and OPA1 gene dosage rescues the mitochondrial morphological defects associated with PINK1 and Parkin mutants
PINK1 and parkin may participate in mitochondrial fusion/fission. Defects in mitochondria morphology/structure and increased rate of lethality in PINK1 and Parkin mutants could be due to altered mitochondrial fission. Perturbation of mitochondrial fission could be a damaging cellular process involving Parkin and PINK1 in PD.
Fission increases disposal of mitochondria
Mitophagy: autophagic disposal of mitochondria
Loss of mitochondrial membrane potential ΔΨm as a functional correlate to mitochondrial damage ΔΨm as a signal to begin mitochondrial removal
Depolarization recruits parkin to the outer mitochondrial membrane
Depolarization induces parkin-mediated clearance specifically of mitochondria
Parkin-mediated clearance of mitochondria occurs via autophagic mechanisms
PINK1 and ΔΨm recruit parkin to the outer mitochondrial membrane to begin mitophagy M E C H A N I S M ?
1- PINK1 mediated recruitment of parkin: Possibly through phosphorylation: dispensable mechanism 2- Role of parkin in mitophagy: * degradation of mfn2: inhibition of fusion, enhancement of fission, which is required for mitophagy * ubiquitination of p62: dispensable * ubiquitination of HDAC6: improved aggresome formation, improved mitophagy
Neurotoxins that induce PD
- 6-hydroxydopamine (6-OHDA) -Paraquat -Rotenone -MPTP 1-They all induce death of dopaminergic neurons; 2-they all increase the production of ROS; 3-they are all good models for the study of the mechanisms and treatments for PD. 4-However, only some cause death by apoptosis and induce accumulation of -synuclein intracellular inclusions.
MPTP, 1-methyl-4-phenyl-1,2,3,6,-tetrahydropyridine MPTP is a by-product in the synthesis of MPPP (1-methyl-4-phenyl-4- propionoxypiperidine, analogue of the narcotic meperidine-Demerol), an illicit narcotic drug. MPTP causes severe, irreversible parkinsonism. MPTP causes strong degenerations of dopaminergic neurons that contain neuromelanin. The mechanism is related to increased production of ROS, through interaction with iron in pigmented neurons (Zecca, 2001). Other substances interact with neuromelanin, suggesting that pigmented neurons are more susceptible to PD. MPTP is highly lipophilic and crossed the brain/blood barrier very quickly.
MPTP: mechanisms of action Generation of the active species MPP + in glial cells. MPTP targets specifically dopaminergic neurons or few other monoaminergic neurons. MPTP is oxidized to MPDP + in glial cells by monoaminoxidase B (MAOB) (present only in DA and serotoninergic neurons). Then, MPDP + is oxidized to MPP +. MPP + exits the glial cell, binds to the DAT (dopamine transporter) and enters the dopaminergic neuron. In this respect DAT activity and/or expression levels are crucial determinants in the susceptibility to PD.
L-DOPA: administered to favor the synthesis of dopamine, remains the most effective medication for PD, and the “gold standard” used to measure all treatments for PD, and to diagnose it (if the patient is responsive to L-DOPA, thus it is PD). Administered together with Carbidopa, to reduce the amount of L-DOPA converted into dopamine in the blood. In this way, more L-DOPA is converted into dopamine in the brain, and smaller doses of L-DOPA lasts longer. After long time of treatment, L- DOPA will eventually stop working. MAOB inhibitors: used to reduce the degradation of dopamine. Selegiline. Used both in the early and late stages of the disease, it improves the effects of L-DOPA. Dopamine receptors’ agonists: they stimulate dopamine receptors mimicking the structure of dopamine. In this way they promote signaling in dopaminergic neurons. (Bromocriptine, Pergolide, apomorphine hydrochloride, Ropinirole). COMT inhibitors: Entacapone, Tolcapone. They inhibit the action of COMT, catechol O-methyltransferase, an enzyme that degrades L-DOPA by catalyzing the methylation of one of the hydroxyl groups in the cathecol nucleus. Administered in the therapy with L-DOPA.
Deep Brain Stimulation (DBS) “Deep brain stimulation (DBS) is a surgical procedure used to treat a variety of disabling neurological symptoms—most commonly the debilitating symptoms of Parkinson’s disease (PD), such as tremor, rigidity, stiffness, slowed movement, and walking problems. DBS uses a surgically implanted, battery-operated medical device called a neurostimulator—similar to a heart pacemaker and approximately the size of a stopwatch—to deliver electrical stimulation to targeted areas in the brain that control movement, blocking the abnormal nerve signals that cause tremor and PD symptoms. The DBS system consists of three components: the lead, the extension, and the neurostimulator. The lead (also called an electrode)—a thin, insulated wire—is inserted through a small opening in the skull and implanted in the brain. The tip of the electrode is positioned within the targeted brain area. The extension is an insulated wire that is passed under the skin of the head, neck, and shoulder, connectng the lead to the neurostimulator. The neurostimulator (the "battery pack") is the third component and is usually implanted under the skin near the collarbone. In some cases it may be implanted lower in the chest or under the skin over the abdomen. Once the system is in place, electrical impulses are sent from the neurostimulator up along the extension wire and the lead and into the brain. These impulses interfere with and block the electrical signals that cause PD symptoms”. From NINDS (National Institue of Neurological Disorders and Stroke)
Sites for surgical intervention in Parkinson’s disease