2018
DOI: 10.3892/etm.2018.6428
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[Erratum] Tanshinone�IIA and Astragaloside�IV promote the angiogenesis of mesenchymal stem cell‑derived endothelial cell‑like cells via upregulation of Cx37, Cx40 and Cx43

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Cited by 17 publications
(14 citation statements)
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“…AS IV also inhibits proliferation and migration of human dermal vascular smooth muscle cells, stimulated by PDGF-BB secreted during vascular injury, through inhibition of p38 MAPK signaling (Chen et al, 2014). It has also been reported that AS IV and Tan IIA promote tubular structure formation of BMSC-derived endothelial cell cells, similar to that of blood vessels, via the expression of connexins and cell connection (Li et al, 2018b).…”
Section: Astragaloside IVmentioning
confidence: 88%
“…AS IV also inhibits proliferation and migration of human dermal vascular smooth muscle cells, stimulated by PDGF-BB secreted during vascular injury, through inhibition of p38 MAPK signaling (Chen et al, 2014). It has also been reported that AS IV and Tan IIA promote tubular structure formation of BMSC-derived endothelial cell cells, similar to that of blood vessels, via the expression of connexins and cell connection (Li et al, 2018b).…”
Section: Astragaloside IVmentioning
confidence: 88%
“…The animal model of intracerebral hemorrhagic brain edema has been widely used to study the etiology and pathology of brain edema in humans (14)(15)(16). Brain edema after cerebral hemorrhage could cause extensive edema (11)(12)(13), and preventing the occurrence or aggravation of brain edema is an important factor to reduce the mortality and disability rates of cerebral hemorrhage (17). The previous animal models were unable to fully reflect the clinical and pathophysiological manifestations of cerebral hemorrhage brain edema (18)(19)(20); therefore, it was very important to establish a compound animal model of cerebral hemorrhage brain edema.…”
Section: Discussionmentioning
confidence: 99%
“…A large number of studies have revealed that whether stem cells develop into cardiomyocytes [59,60] and vascular endothelial cells [61][62][63] or differentiate into neurons [64][65][66] and osteoblasts [67,68], the Shh signaling pathway plays an important role. Astragaloside IV promoted mesenchymal stem cells into neuronal cells [69], endothelial cells [22], and cardiomyocytes [70]. e angiogenesis and cardiomyocyte survival induced by astragaloside IV in rats with acute Evidence-Based Complementary and Alternative Medicine myocardial infarction attributed to upregulation of the gene expression of Shh pathway and their activity of receptors and signal transducers [71].…”
Section: Shh/gli1mentioning
confidence: 99%
“…Our previous studies have found that bavachalcone, an isopentenyl chalcone from Psoralea corylifolia Linn., promoted the differentiation of EPCs and neovascularization in vivo [19]. In a series of cell-based experiments, Tang and his colleagues observed that ginkgolide B, icariin, tanshinone IIA, astragaloside IV, ginsenoside Rg1, and salidroside exert angiogenic endothelial differentiation effects of human bone marrow-derived EPCs [20][21][22][23][24]. A study reported that salvianolic acid A could augment EPC numbers and promote EPC migration, adhesion, and the vasculogenesis capacity in myocardial ischemia-reperfusion (I/R) rat model [25].…”
Section: Endothelial Cell and Cardiomyocyte Differentiationmentioning
confidence: 99%