Molecular Biology and Genetics of Amyotrophic Lateral Sclerosis
Molecular Biology and Genetics of Amyotrophic Lateral Sclerosis Michael Sidel February 13, 2008
Goals • To have a basis for the understanding of the genetics involved in ALS • To understand the current theories and concepts that underlie the pathogenesis of ALS
Outline • Brief clinical overview of the disease – 1 slide • The genetics of ALS – 6 Slides • The pathology of ALS – 5 Slides • An understanding of the disease pathogenesis – Priceless (or 8 slides)
Some Clinical Factoids about ALS • • A progressive neurodegenerative disease Involvement of motor neurons at all levels 50% mortality at 3 years Several clinically related variants: – Primary lateral sclerosis – Primary muscular atrophy – Progressive bulbar palsy • 90% of the cases are considered “sporadic” • 10% of cases are considered familial
Some of the Genetics of ALS
Genetics of ALS • 10% of cases of ALS have history of firstdegree relative with the disease – Suggests Autosomal Dominant inheritance • Research direction: – Isolating genes involved in clear familial disease – Isolating polymorphisms that are potentially risk factors in sporadic disease
Genetics of Familial ALS Mitchell and Borasio, Lancet 2007; 369: 2031– 41
Genetics of Familial ALS Mitchell and Borasio, Lancet 2007; 369: 2031– 41
Genetics of Familial ALS Mitchell and Borasio, Lancet 2007; 369: 2031– 41
Genetics of Familial ALS Mitchell and Borasio, Lancet 2007; 369: 2031– 41
Genetics of Familial ALS • Represents 10 -20% of cases of familial ALS • Over 100 mutations to the gene are related to pathology • Gain of function mutation causes the disease pathology – From mouse model data
Genetics of Familial ALS Mitchell and Borasio, Lancet 2007; 369: 2031– 41
Genetics of Familial ALS Mitchell and Borasio, Lancet 2007; 369: 2031– 41
Genetics Associations in ALS • There are other genetic mutations that may alter the risk of developing ALS: • Examples: – Angiogenin (14 q 11. 2) – Vascular endothelial growth factor (6 p 12) – Survival motor neuron (5 q 12. 2 -q 13. 3) – Neurofilament protein (22 q 12. 2) – Multivesicular body protein 2 B (2 p 11. 2)
PATHOLOGY OF ALS
Gross Pathology • Motor neuron degeneration and death with gliosis • Gliosis of the CST • Atrophy of ventral nerve roots
Microscopic Pathology • Intracellular inclusions - Bunina bodies - Ubiquinated inclusions (not tau)
PATHOGENIC MECHANISMS OF ALS
Proposed Pathogenic Mechanisms in ALS • Oxidative Stress • Excitotoxicity • Abnormal Protein Precipitation and/or Aggregation • Cytoskeletal defects • Axonal transport • Neuroinflammation • Abnormalities in hypoxia-regulated genes • Apoptosis
Oxidative Stress • Motor neuron damage as a result of oxidative stress • Not necessarily linked to gene mutation – i. e. SOD 1 • Post-mortem studies have shown evidence of increased oxidative byproducts • Linked to other mechanisms
Excitotoxicity • Glutamate mediated • Possible mechanisms of disease include: – Production of free radicals – Increased intracellular calcium • Decreased EAAT 2 functions has been described in some ALS post-mortem studies
More on Excitoxocity Goodall and Morrison Expert Reviews in Molecular Medicine. Vol. 8(11) 24 May 2006.
Abnormal Protein Precipitation and/or Aggregation • Abnormal protein aggregates, including Bunina bodies, ubiquitinated inclusions and neurofilament rich hyaline inclusions are pathological hallmarks of ALS • Unknown cause and effect relationship • SOD 1 mutants can misfold and coprecipitate with other molecules as well
Cytoskeletal Defects • Neurofilament proteins are the most abundant structural protein in motor neurons, and aggregates of neurofilament proteins motor neurons are commonly seen in ALS • Can be found as part of inclusions • Overexpression of peripherin or alphainternexin in mice can cause motor neuron disease
Axonal Transport • Axonal transport of materials is essential for neuronal function and survival • Dynactin is a protein involved in fast retrograde transport in the axon • Mutations in this gene have been associated with motor neuron disease
Neuroinflammation • Microglia have been found to be activated in parts of CNS affected by ALS • COX-2 Receptors and downstream prostaglandins are elevated in ALS brains
Apoptosis • Represents eneergy-dependent programmed cell death • In human ALS spinal cord tissue, increases in caspase-1 and -9 activation have been detected • Very unclear how much this plays a role in the pathogenesis of the disease
Goodall and Morrison. Expert Reviews in Molecular Medicine. Vol. 8(11) 24 May 2006.
Why Motor Neurons? • • • Extreme size of cells High metabolic activity Sensitivity to mitochondrial dysfunction Elevated neurofilament content Reduced capacity to buffer calcium
Conclusions • We do not understand ALS • Familial ALS is caused by genetic mutations and is rare • Sporadic ALS is caused by a combination of: – Genetic susceptibility – Environmental triggers – Motor neuron specific cellular damage
Key Points to Remember 1. Main cause of familial ALS is SOD 1 mutations with are gain of function 2. Bunina bodies are inclusions found in ALS motor neurons 3. Excitoxicity and oxidative damage are likely major contributors to motor neuron death in ALS
References • Valdmanis, P. N. and Rouleau, G. A. Genetics of familial amyotrophic lateral sclerosis. Neurology. 2008; 70: 144 -152. • Goodall, E. F. and Morrison, K. E. Amyotrophic lateral sclerosis: proposed mechanisms and pathways to treatment. Expert Reviews in Molecular Medicine. Vol. 8; Issue 11; 24 May 2006. • Mitchell, J. D. and Barasio, G. D. Amyoptrophic Lateral Sclerosis. Lancet 2007; 369: 2031 -41.
- Slides: 34