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Merck
  • Derivation of keratinocytes from chicken embryonic stem cells: establishment and characterization of differentiated proliferative cell populations.

Derivation of keratinocytes from chicken embryonic stem cells: establishment and characterization of differentiated proliferative cell populations.

Stem cell research (2015-02-24)
Mathilde Couteaudier, Laëtitia Trapp-Fragnet, Nicolas Auger, Katia Courvoisier, Bertrand Pain, Caroline Denesvre, Jean-François Vautherot
要旨

A common challenge in avian cell biology is the generation of differentiated cell-lines, especially in the keratinocyte lineage. Only a few avian cell-lines are available and very few of them show an interesting differentiation profile. During the last decade, mammalian embryonic stem cell-lines were shown to differentiate into almost all lineages, including keratinocytes. Although chicken embryonic stem cells had been obtained in the 1990s, few differentiation studies toward the ectodermal lineage were reported. Consequently, we explored the differentiation of chicken embryonic stem cells toward the keratinocyte lineage by using a combination of stromal induction, ascorbic acid, BMP4 and chicken serum. During the induction period, we observed a downregulation of pluripotency markers and an upregulation of epidermal markers. Three homogenous cell populations were derived, which were morphologically similar to chicken primary keratinocytes, displaying intracellular lipid droplets in almost every pavimentous cell. These cells could be serially passaged without alteration of their morphology and showed gene and protein expression profiles of epidermal markers similar to chicken primary keratinocytes. These cells represent an alternative to the isolation of chicken primary keratinocytes, being less cumbersome to handle and reducing the number of experimental animals used for the preparation of primary cells.

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製品内容

Sigma-Aldrich
Triton X-100, laboratory grade
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コレラ菌由来毒素 コレラ菌由来, ≥90% (SDS-PAGE), lyophilized powder
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L-グルタミン, meets USP testing specifications, suitable for cell culture, 99.0-101.0%, from non-animal source
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L-アスコルビン酸, powder, suitable for cell culture, γ-irradiated
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ヨウ化プロピジウム, ≥94.0% (HPLC)
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ヒドロコルチゾン, BioReagent, suitable for cell culture
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エチルアルコール(純粋), 190 proof, ACS spectrophotometric grade, 95.0%
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マイトマイシンC Streptomyces caespitosus由来, powder, BioReagent, suitable for cell culture
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L-アスコルビン酸, BioXtra, ≥99.0%, crystalline
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L-アスコルビン酸, suitable for cell culture, suitable for plant cell culture, ≥98%
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エタノール, JIS special grade, ≥99.5%
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L-アスコルビン酸, 99%
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L-アスコルビン酸, reagent grade, crystalline
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アスコルビン酸, Pharmaceutical Secondary Standard; Certified Reference Material
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L-グルタミン, ReagentPlus®, ≥99% (HPLC)
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ヒドロコルチゾン, γ-irradiated, powder, BioXtra, suitable for cell culture
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アデニン, ≥99%
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セレン, powder, −100 mesh, 99.99% trace metals basis
USP
アスコルビン酸, United States Pharmacopeia (USP) Reference Standard
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ヒドロコルチゾン, ≥98% (HPLC)
SAFC
L-グルタミン
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セレン, powder, −100 mesh, ≥99.5% trace metals basis
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マイトマイシンC Streptomyces caespitosus由来, ≥98% (HPLC), γ-irradiated, suitable for cell culture
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ヒドロコルチゾン-水溶性, BioReagent, suitable for cell culture
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L-アスコルビン酸, ACS reagent, ≥99%
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N,O-ビス(トリメチルシリル)アセトアミド, synthesis grade, ≥95%
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マイトマイシンC Streptomyces caespitosus由来, powder, contains NaCl as solubilizer
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L-アスコルビン酸, analytical standard
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エタノール, purum, fine spirit, denaturated with 4.8% methanol, F25 METHYL1, ~96% (based on denaturant-free substance)
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ヨウ化プロピジウム 溶液