2004
DOI: 10.1016/j.brainres.2004.09.061
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Expression of insulin-like growth factor 1 and receptor in ischemic rats treated with human marrow stromal cells

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Cited by 153 publications
(118 citation statements)
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“…39,44 Although various growth factors are released from ischemic tissue, the factor responsible for promoting neuroblast differentiation appears to be unknown. Previous studies have shown that IGF-I is upregulated following ischemic injury, 45,46 and exogenous infusion of IGF-I enhances neural progenitor cell proliferation. 11 In contrast, other studies have shown that IGF-I induces the differentiation of neural progenitor cells 26 and, more specifically, instructs the differentiation of oligodendrocytes.…”
Section: Role Of Neural Stem Cellsmentioning
confidence: 97%
“…39,44 Although various growth factors are released from ischemic tissue, the factor responsible for promoting neuroblast differentiation appears to be unknown. Previous studies have shown that IGF-I is upregulated following ischemic injury, 45,46 and exogenous infusion of IGF-I enhances neural progenitor cell proliferation. 11 In contrast, other studies have shown that IGF-I induces the differentiation of neural progenitor cells 26 and, more specifically, instructs the differentiation of oligodendrocytes.…”
Section: Role Of Neural Stem Cellsmentioning
confidence: 97%
“…63 Several reports have focused on the role of neurotrophic factors such as an increase in insulin growth factor-1 (IGF1) and its receptor which may play a role in neuronal differentiation. Others have suggested that transplanted MSCs facilitate recovery from brain and spinal cord lesions by releasing brain natriuretic peptide (BNP) and other vasoactive factors to reduce edema, decrease intracranial pressure and improve cerebral perfusion.…”
Section: Human Mscsmentioning
confidence: 99%
“…24 h Produced many trophic factors; monocyte chemoattractant protein-1 [26,27] levels signifi cantly increased from 6 h, peaked at 48 h after MCAO, and enhanced BMSC migration and tissue repair Transient MCAO (2 h)/ i.v. 24 h hMSCs expressed bFGF and VEGF, promoted expression of insulin- [28][29][30] Permanent MCAO like growth factor 1 and receptor, which contributed to improved recovery and increased neurogenesis Transient MCAO (2 h) i.v. 24 h Cell-free MSC-generated exosomes survived, enhanced neurite [31,32] remodeling and angiogenesis, and improved functional recovery;…”
Section: Ischemic Strokementioning
confidence: 99%