2013
DOI: 10.1016/j.neuroscience.2013.05.034
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Systemic treatment with adipose-derived mesenchymal stem cells ameliorates clinical and pathological features in the amyotrophic lateral sclerosis murine model

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Cited by 127 publications
(106 citation statements)
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“…In the last decade, several studies have demonstrated that the therapeutic potential of ASCs could be due to their paracrine activity rather than to their integration and survival in host tissues. [4][5][6] In particular, the paracrine mechanism seems to be mediated through exosomes release, making exosomes a potential alternative to cell therapy in neurodegenerative diseases.…”
Section: Discussionmentioning
confidence: 99%
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“…In the last decade, several studies have demonstrated that the therapeutic potential of ASCs could be due to their paracrine activity rather than to their integration and survival in host tissues. [4][5][6] In particular, the paracrine mechanism seems to be mediated through exosomes release, making exosomes a potential alternative to cell therapy in neurodegenerative diseases.…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3] Moreover, it has been recently demonstrated that in vivo administration of ASCs ameliorates the disease condition in several neurodegenerative animal models. [4][5][6] In particular, it has been reported that transplantation of autologous ASCs has a therapeutic effect in experimental autoimmune encephalomyelitis and in murine model of familial amyotrophic…”
Section: Introductionmentioning
confidence: 99%
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“…Marconi et al assessed the efficacy of the systemic administration of adipose-derived mesenchymal stem cells (ASC) in SOD1-mutant mice and found that the cells not only significantly delayed motor deterioration for 4-6 weeks and maintained the number of motor neurons but also up-regulated the levels of glialderived neurotrophic factor (GDNF) and basic fibroblast growth factor (bFGF) in the spinal cord. Given that ASCs produce bFGF but not GDNF, these findings indicated that ASCs may promote neuroprotection either directly and/or by modulating the response of local glial cells toward a neuroprotective phenotype [40]. Similarly, intramuscular transplantation of MSCs engineered to secrete GDNF was found to attenuate motor neuron loss and prolong the lifespan of ALS rats [41].…”
Section: Mesenchymal Stromal Cellsmentioning
confidence: 99%
“…Embryonic Stem Cells: By using embryonic stem cells (ES cells) from mice carrying transgenic alleles of SOD1 gene to generate motor neurons in vitro [50], in 2011 Wyatt TJ et al, transplanted these ES cells into SOD1G93A rodent model of ALS results in enhancing the numbers of endogenous neurons [51].…”
Section: In-vitro Trials Involving Mechanisms Of Stem Cell-mentioning
confidence: 99%