Bone-marrow-derived mesenchymal stem cell therapy for neurodegenerative diseases

Expert Opin Biol Ther. 2009 Dec;9(12):1487-97. doi: 10.1517/14712590903321439.

Abstract

Background: Stem-cell-based therapy is a promising new approach to handling neurodegenerative diseases. One of the most promising cellular sources is bone-marrow-derived mesenchymal stem cells (MSCs) also termed multipotent stromal cells. MSCs represent an autologous source and are abundant and non-tumorigenic. Additionally, MSCs possess the useful characteristics of homing and chemokine secretion.

Objective/methods: Since neurodegenerative diseases have many pathological processes in common, a specific therapeutic agent could potentially ameliorate the symptoms of several distinct neurodegenerative diseases. In this review we demonstrate the wide variety of mechanisms by which MSCs can influence neurodegenerative processes.

Results/conclusions: The mechanisms by which transplanted MSCs influence neurodegenerative diseases can be broadly classified as cellular replacement or paracrine secretion, with the latter subdivided into trophic factor secretion or immunomodulation by cytokines. Emerging research suggests that genetic manipulations before transplantation could enhance the therapeutic potential of MSCs. Such manipulation could turn the cells into a 'Trojan horse', to deliver specific proteins, or promote reprogramming of the MSCs into the neural lineage. Clinical trials testing MSC-based therapies for familial amyotrophic lateral sclerosis and multiple sclerosis are in progress.

Publication types

  • Review

MeSH terms

  • Animals
  • Bone Marrow Transplantation* / adverse effects
  • Cell Movement
  • Combined Modality Therapy
  • Cytokines / immunology
  • Genetic Therapy
  • Humans
  • Mesenchymal Stem Cell Transplantation* / adverse effects
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / immunology
  • Neurodegenerative Diseases / surgery*
  • Neurogenesis
  • Neurons / immunology
  • Neurons / transplantation*
  • Paracrine Communication
  • Transplantation, Autologous
  • Treatment Outcome

Substances

  • Cytokines