Targeting STMN2 for neuroprotection and neuromuscular recovery in Spinal Muscular Atrophy: evidence from in vitro and in vivo SMA models

Cell Mol Life Sci. 2024 Dec 27;82(1):29. doi: 10.1007/s00018-024-05550-3.

Abstract

The development of ground-breaking Survival Motor Neuron (SMN) replacement strategies has revolutionized the field of Spinal Muscular Atrophy (SMA) research. However, the limitations of these therapies have now become evident, highlighting the need for the development of complementary targets beyond SMN replacement. To address these challenges, here we explored, in in vitro and in vivo disease models, Stathmin-2 (STMN2), a neuronal microtubule regulator implicated in neurodegenerative diseases like Amyotrophic Lateral Sclerosis (ALS), as a novel SMN-independent target for SMA therapy. Our findings revealed that STMN2 overexpression effectively restored axonal growth and outgrowth defects in induced pluripotent stem cell-(iPSC)-derived motor neurons (MNs) from SMA patients. Intracerebroventricular administration of adeno-associated virus serotype 9 (AAV9) carrying Stmn2 cDNA significantly ameliorated survival rates, motor functions, muscular and neuromuscular junction pathological features in SMA mice, mirrored by in vitro outcomes. Overall, this pioneering study not only provides insight into the therapeutic potential of STMN2 in SMA, but also suggests its broader applications for MN diseases, marking a substantial step forward in addressing the multifaceted challenges of neurological diseases treatment.

Keywords: Modifier gene; Motor neurons; SMA mouse; SMN; STMN2.

MeSH terms

  • Animals
  • Dependovirus / genetics
  • Disease Models, Animal*
  • Genetic Therapy / methods
  • Humans
  • Induced Pluripotent Stem Cells* / cytology
  • Induced Pluripotent Stem Cells* / metabolism
  • Mice
  • Motor Neurons* / metabolism
  • Motor Neurons* / pathology
  • Muscular Atrophy, Spinal* / genetics
  • Muscular Atrophy, Spinal* / metabolism
  • Muscular Atrophy, Spinal* / pathology
  • Muscular Atrophy, Spinal* / therapy
  • Neuromuscular Junction / metabolism
  • Neuromuscular Junction / pathology
  • Neuroprotection
  • Stathmin* / genetics
  • Stathmin* / metabolism

Substances

  • Stathmin
  • STMN2 protein, human