2016
DOI: 10.1021/acs.jafc.5b05661
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Pleurotus eryngii Polysaccharide Promotes Pluripotent Reprogramming via Facilitating Epigenetic Modification

Abstract: Pleurotus eryngii is a medicinal/edible mushroom with great nutritional value and bioactivity. Its polysaccharide has recently been developed into an effective gene vector via cationic modification. In the present study, cationized P. eryngii polysaccharide (CPS), hybridized with calcium phosphate (CP), was used to codeliver plasmids (Oct4, Sox2, Klf4, c-Myc) for generating induced pluripotent stem cells (iPSCs). The results revealed that the hybrid nanoparticles could significantly enhance the process and eff… Show more

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Cited by 10 publications
(7 citation statements)
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References 48 publications
(69 reference statements)
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“…The colonies were released from the scaffolds and expanded on feeder layers which were then examined for pluripotent marker expression. An average of 306 cell spheres was released from each scaffold, making the reprogramming efficiency of 0.306% (from the original 1 × 10 5 cells/scaffold), which was significantly higher than that of the previously reported 2D nonviral iPSC-generating system (0.128%) . The bright-field images showcased the tightly packed morphology of the colonies on the 2D feeder layers (Figure a).…”
Section: Resultsmentioning
confidence: 75%
See 1 more Smart Citation
“…The colonies were released from the scaffolds and expanded on feeder layers which were then examined for pluripotent marker expression. An average of 306 cell spheres was released from each scaffold, making the reprogramming efficiency of 0.306% (from the original 1 × 10 5 cells/scaffold), which was significantly higher than that of the previously reported 2D nonviral iPSC-generating system (0.128%) . The bright-field images showcased the tightly packed morphology of the colonies on the 2D feeder layers (Figure a).…”
Section: Resultsmentioning
confidence: 75%
“…An average of 306 cell spheres was released from each scaffold, making the reprogramming efficiency of 0.306% (from the original 1 × 10 5 cells/scaffold), which was significantly higher than that of the previously reported 2D nonviral iPSCgenerating system (0.128%). 42 The bright-field images showcased the tightly packed morphology of the colonies on the 2D feeder layers (Figure 6a). In addition, the colonies from the 3D system and the human ESCs shared expression similar to that of pluripotent markers such as SSEA3, TRA-1−81, NANOG, and OCT4 (Figure 6b).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Moreover, hybrid nanocarriers internalize plasmids in multiple ways, which in turn increase their reprograming efficiency. [ 258 ] Furthermore, they were applied into a 3D collagen hydrogel to produce 3D cell spheres with tightly packed cloned expressed iPSC markers. [ 259 ]…”
Section: Cell Reprogramming By Nonviral Vectorsmentioning
confidence: 99%
“…Moreover, hybrid nanocarriers internalize plasmids in multiple ways, which in turn increase their reprograming efficiency. [258] Furthermore, they were applied into a 3D collagen hydrogel to produce 3D cell spheres with tightly packed cloned expressed iPSC markers. [259] Concerning reports of potential toxicity (linked to high molecular weight) of branched PEI limit their application as nanocarriers.…”
Section: Hybrid Nanocarriersmentioning
confidence: 99%
“…It has been reported that crude PEP could be purified by DEAE-52 cellulose and Sephadex G-100 (Chen et al, 2013;Deng et al, 2016). Herein, we successfully utilised D101 macroporous adsorptive resin and DEAE-52 cellulose to purify crude PEP to obtain two homogeneous polysaccharides.…”
Section: Monosaccharide Composition Of Ppep-1 and Ppep-2mentioning
confidence: 99%