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Natsuko Kakudo

Researcher at Kansai Medical University

Publications -  119
Citations -  1884

Natsuko Kakudo is an academic researcher from Kansai Medical University. The author has contributed to research in topics: Medicine & Platelet-rich plasma. The author has an hindex of 19, co-authored 97 publications receiving 1553 citations.

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Proliferation-promoting effect of platelet-rich plasma on human adipose-derived stem cells and human dermal fibroblasts.

TL;DR: Clinical platelet-rich plasma application for cell-based, soft-tissue engineering and wound healing is supported, as its activation was associated with the release of large amounts of PDGF-AB and TGF-&bgr;1 and its activation promoted the proliferation of human adipose–derived stem cells and human dermal fibroblasts.
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Fibroblast growth factor-2 stimulates adipogenic differentiation of human adipose-derived stem cells.

TL;DR: FGF-2 significantly enhances the adipogenic differentiation of human ASCs, as induced by an adipogenic hormonal cocktail consisting of 3-isobutyl-1-methylxanthine (IBMX), dexamethasone, insulin, and indomethacin.
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Platelet and growth factor concentrations in activated platelet-rich plasma: a comparison of seven commercial separation systems.

TL;DR: The composition of PRP produced by commercially available separation systems was characterized, and the mean PDGF-AB concentration of activated PRP was the highest from JP200, followed by the KYOCERA Medical PRP Kit, Magellan Autologous Platelet Separator System, MyCells, and GLO PRP.
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Bone tissue engineering using human adipose-derived stem cells and honeycomb collagen scaffold

TL;DR: Honeycomb collagen scaffold is a suitable scaffold for ASCs and will be useful as a three-dimensional bone tissue engineering scaffold in vitro and in vivo, according to histological views.
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Hypoxia Enhances Proliferation of Human Adipose-Derived Stem Cells via HIF-1ɑ Activation

TL;DR: Adipose tissue-derived stem cells (ASCs) isolated from human subcutaneous adipose tissue were cultured in hypoxic or normoxic conditions and proliferation was significantly enhanced in the hypoxic culture and was inhibited by ERK and Akt inhibitors.