PUBLICATION

The Power of Human Protective Modifiers: PLS3 and CORO1C Unravel Impaired Endocytosis in Spinal Muscular Atrophy and Rescue SMA Phenotype

Authors
Hosseinibarkooie, S., Peters, M., Torres-Benito, L., Rastetter, R.H., Hupperich, K., Hoffmann, A., Mendoza-Ferreira, N., Kaczmarek, A., Janzen, E., Milbradt, J., Lamkemeyer, T., Rigo, F., Bennett, C.F., Guschlbauer, C., Büschges, A., Hammerschmidt, M., Riessland, M., Kye, M.J., Clemen, C.S., Wirth, B.
ID
ZDB-PUB-160809-7
Date
2016
Source
American journal of human genetics   99(3): 647-65 (Journal)
Registered Authors
Hammerschmidt, Matthias
Keywords
none
MeSH Terms
  • Actins/metabolism
  • Animals
  • Axons/pathology
  • Calcium/metabolism
  • Carrier Proteins
  • Disease Models, Animal
  • Endocytosis/genetics*
  • Humans
  • Male
  • Membrane Glycoproteins/genetics*
  • Membrane Glycoproteins/metabolism*
  • Mice
  • Microfilament Proteins/genetics*
  • Microfilament Proteins/metabolism*
  • Muscular Atrophy, Spinal/genetics*
  • Muscular Atrophy, Spinal/pathology*
  • Neuromuscular Junction/metabolism
  • Neuromuscular Junction/pathology
  • Oligonucleotides, Antisense
  • Phenotype
  • Presynaptic Terminals/metabolism
  • Pyridinium Compounds/metabolism
  • Quaternary Ammonium Compounds/metabolism
  • Survival of Motor Neuron 1 Protein/genetics
  • Survival of Motor Neuron 2 Protein/genetics
  • Synaptic Transmission/genetics
  • Zebrafish/genetics
  • Zebrafish/metabolism
PubMed
27499521 Full text @ Am. J. Hum. Genet.
Abstract
Homozygous loss of SMN1 causes spinal muscular atrophy (SMA), the most common and devastating childhood genetic motor-neuron disease. The copy gene SMN2 produces only ∼10% functional SMN protein, insufficient to counteract development of SMA. In contrast, the human genetic modifier plastin 3 (PLS3), an actin-binding and -bundling protein, fully protects against SMA in SMN1-deleted individuals carrying 3-4 SMN2 copies. Here, we demonstrate that the combinatorial effect of suboptimal SMN antisense oligonucleotide treatment and PLS3 overexpression-a situation resembling the human condition in asymptomatic SMN1-deleted individuals-rescues survival (from 14 to >250 days) and motoric abilities in a severe SMA mouse model. Because PLS3 knockout in yeast impairs endocytosis, we hypothesized that disturbed endocytosis might be a key cellular mechanism underlying impaired neurotransmission and neuromuscular junction maintenance in SMA. Indeed, SMN deficit dramatically reduced endocytosis, which was restored to normal levels by PLS3 overexpression. Upon low-frequency electro-stimulation, endocytotic FM1-43 (SynaptoGreen) uptake in the presynaptic terminal of neuromuscular junctions was restored to control levels in SMA-PLS3 mice. Moreover, proteomics and biochemical analysis revealed CORO1C, another F-actin binding protein, whose direct binding to PLS3 is dependent on calcium. Similar to PLS3 overexpression, CORO1C overexpression restored fluid-phase endocytosis in SMN-knockdown cells by elevating F-actin amounts and rescued the axonal truncation and branching phenotype in Smn-depleted zebrafish. Our findings emphasize the power of genetic modifiers to unravel the cellular pathomechanisms underlying SMA and the power of combinatorial therapy based on splice correction of SMN2 and endocytosis improvement to efficiently treat SMA.
Genes / Markers
Figures
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Expression
Phenotype
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping
Errata and Notes