Transplantation of Neural Progenitor Cells Expressing Glial Cell Line-Derived Neurotrophic Factor into the Motor Cortex as a Strategy to Treat Amyotrophic Lateral Sclerosis

Author:

Thomsen Gretchen M.12ORCID,Avalos Pablo1,Ma Annie A.1,Alkaslasi Mor1,Cho Noell1,Wyss Livia1,Vit Jean-Philippe23,Godoy Marlesa1,Suezaki Patrick1,Shelest Oksana1,Bankiewicz Krystof S.4,Svendsen Clive N.12

Affiliation:

1. Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA

2. Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA

3. Biobehavioral Research Core, Cedars-Sinai Medical Center, Los Angeles, California, USA

4. Department of Neurological Surgery, University of California, San Francisco, California, USA

Abstract

Abstract Early dysfunction of cortical motor neurons may underlie the initiation of amyotrophic lateral sclerosis (ALS). As such, the cortex represents a critical area of ALS research and a promising therapeutic target. In the current study, human cortical-derived neural progenitor cells engineered to secrete glial cell line-derived neurotrophic factor (GDNF) were transplanted into the SOD1G93A ALS rat cortex, where they migrated, matured into astrocytes, and released GDNF. This protected motor neurons, delayed disease pathology and extended survival of the animals. These same cells injected into the cortex of cynomolgus macaques survived and showed robust GDNF expression without adverse effects. Together this data suggests that introducing cortical astrocytes releasing GDNF represents a novel promising approach to treating ALS.

Funder

ALS Finding a Cure Foundation

The ALS Association

Department of Defense

ALS Association

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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