JP2017197501A - セマフォリン3a発現亢進剤 - Google Patents
セマフォリン3a発現亢進剤 Download PDFInfo
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- JP2017197501A JP2017197501A JP2016091429A JP2016091429A JP2017197501A JP 2017197501 A JP2017197501 A JP 2017197501A JP 2016091429 A JP2016091429 A JP 2016091429A JP 2016091429 A JP2016091429 A JP 2016091429A JP 2017197501 A JP2017197501 A JP 2017197501A
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- semaphorin
- expression
- ceramide
- kcer
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Abstract
Description
項1. 植物由来スフィンゴ糖脂質及び/又はセラミドを有効成分とするセマフォリン3A発現亢進剤。
項2. 植物由来スフィンゴ糖脂質及び/又はセラミドが、コンニャク由来である項1に記載のセマフォリン3A発現亢進剤。
項3.項1又は2に記載のセマフォリン3A発現亢進剤を含有するセマフォリン3A発現亢進用の皮膚外用剤。
本発明のセマフォリン3A発現亢進剤は、植物由来スフィンゴ糖脂質及び/又はセラミドを有効成分とする。
スフィンゴ糖脂質とは、スフィンゴイドに脂肪酸がアミド結合した構造のセラミドの第1級アルコール性ヒドロキシ基に糖が結合した糖脂質である。
セラミドは、スフィンゴイドに脂肪酸がアミド結合した構造を有する。本発明において使用されるセラミドとしては、前述した植物由来のセラミドであることを限度として特に限定されず、スフィンゴイドの構造、結合している脂肪酸の構造等については、前記スフィンゴ糖脂質の欄で例示したものと同様である。
本発明のセマフォリン3A発現亢進剤は、前述した植物由来スフィンゴ糖脂質及び/又はセラミド以外に、本発明の効果を損なわない範囲で、剤型に応じて、他の添加成分を含有していてもよい。本発明のセマフォリン3A発現亢進剤に含有され得る添加成分としては、例えば、水、油脂類、ロウ類、炭化水素類、脂肪酸類、高級アルコール類、エステル類、植物抽出エキス類、水溶性高分子、界面活性剤、金属石鹸、アルコール、多価アルコール、pH調整剤、酸化防止剤、紫外線吸収剤、防腐剤、香料、粉体、増粘剤、色素、キレート剤などが挙げられる。これらの添加成分は、1種単独で使用してもよく、また2種以上を組み合わせて使用してもよい。また、これらの添加成分の含有量については、使用する添加成分の種類や本発明のセマフォリン3A発現亢進剤の剤型などに応じて適宜設定される。
本発明のセマフォリン3A発現亢進剤の剤型については、特に限定されず、固体状、半固体状、又は液体状のいずれであってもよく、当該セマフォリン3A発現亢進剤の種類や用途に応じて適宜設定すればよい。
コンニャク由来グルコシルセラミド(kGluCer)(NS170302 Glucosylceramide, from Konjac,純度≧99% (TLC) (株)長良サイエンス)に、Rhodococcus equi M−750株由来のEGCase Iを用いて加水分解を行って、グルコースを遊離させ、コンニャク由来セラミド(kCer)を得た。
正常ヒト表皮角化細胞(NHEK)における軸索ガイダンス分子の発現に対するコンニャク由来セラミド(kCer)の作用
正常ヒト表皮角化細胞(NHEK)を、Lonza社のプロトコルに従い、6ウェル組織培養プレート内で培養した。その後、前記1.で得られたコンニャク由来セラミド(kCer)を最終濃度0、25、50、又は100μMとなるよう添加し、添加して48時間後にtotal RNA及び培養上清を回収し、ヒトSema3AのmRNA発現量と、培養上清中に分泌されたSema3A量の測定を行った。
Total RNAは、製造業者の取扱説明書に従って、RNeasy Mini Kit (QIAGEN)を用いて培養細胞から抽出し、PrimeScript RT reagent kit(Takara,Shiga,Japan)を用いて、cDNAに逆転写し、定量リアルタイムPCRによりヒトSema3AのmRNAの発現量を測定した。定量リアルタイムPCRは製造業者の取扱説明書に従い、SYBR Premix EX Taq(Takara)を使用して、Applied Biosystems 7900HT Fast Real−time PCR system(Applied Biosystems)により実施した。使用したプライマーに関する情報を表1に示す。リボソームタンパク質S18(RPS18)を基準遺伝子として使用した。mRNA量は、RPS18のmRNA量に対して標準化し、そして最終的に未処理対照(kCerの添加量が0μMのもの)のmRNAに対する比として示した。
ELISAは製造業者の取扱説明書に従って、ELISA kit for human semaphorin3A(Uscn, Wuhan, China)を用いて行った。
NHEKに対するkCerの細胞毒性試験
実験例1と同条件でNHEKを96ウェル組織培養プレート内で培養し、最終濃度0、25、50、100μMのkCerを添加後、一定時間経過後(LDHアッセイは2時間後、MTTアッセイは48時間後)に、急性毒性の評価として乳酸脱水素酵素(LDH)アッセイ、亜急性毒性の評価としてMTTアッセイを行った。
LDHアッセイは製造業者の取扱説明書に従って、Cytotoxicity Detection Kit PLUS (LDH)(Roche, Basel, Switzerland)を用いて行った。kCer添加2時間後に培養上清を回収し、それらを反応溶液と30分間反応後、停止溶液を添加し、波長490nmの吸光度を測定した。細胞障害率(%)を「(kCer添加群の平均値/溶媒対照群の吸光度の平均値)×100」の式から求め、細胞生存率(%)を「100−細胞障害率」の式によって求めた。
MTTアッセイは製造業者の取扱説明書に従って、Cell−counting kit 8(Dojindo,Kumamoto,Japan)を用いて行った。kCer添加48時間後にCell−Counting Kit−8溶液を細胞に添加し、一定時間経過後に波長450nmの吸光度を測定した。生細胞率(%)は「各ウェルの吸光度/溶媒対照群の吸光度の平均値×100」の式により求めた。
得られたデータについて、実験例1と同様に、統計ソフトGraphPad Prism(GraphPad Software Inc.,CA,USA)を用いてBonferroni法による有意差検定による解析を行った。P<0.05を統計学的に有意差有りとした。
ドライスキンモデルマウスの病変部に対するkCerの作用
ドライスキンモデルマウスの病変部にkCer溶液を外用する実験を行った。ICRマウス(10週齢)の除毛した腰背部にアセトン溶液を浸した脱脂綿を5分間静置することで、急性ドライスキンモデルを作成した。マウスは(i)未処置、(ii)アセトン処理後すぐに溶媒のエタノールのみ塗布、(iii)アセトン処理後すぐに0.1%kCer塗布の3群(各群6匹)に分類した。各試料の塗布はアセトン処理後1回のみとした。ドライスキン誘発前後で経時的に経表皮水分蒸散量(TEWL)の測定を行った。アセトン処理の48時間後に皮膚を摘出し、0.02%トリプシン/EDTA溶液に一晩浸漬後、表皮を剥離して、RNAを抽出した。その後、定量リアルタイムPCRで表皮におけるSema3A mRNAの発現量を解析した。使用したプライマーを表3に示す。
また、図5に、アセトン処理48時間後の表皮中のSema3A転写レベルを示す。0.1%kCer塗布群は、未処理群及びエタノール塗布群と比較して、表皮のSema3A転写レベルは有意に(*P<0.05,***P<0.001)促進された。この結果は、kCerがSema3Aの発現を亢進し得ることを示唆する。
Claims (3)
- 植物由来スフィンゴ糖脂質及び/又はセラミドを有効成分とするセマフォリン3A発現亢進剤。
- 植物由来スフィンゴ糖脂質及び/又はセラミドが、コンニャク由来である請求項1に記載のセマフォリン3A発現亢進剤。
- 請求項1又は2に記載のセマフォリン3A発現亢進剤を含有するセマフォリン3A発現亢進用の皮膚外用剤。
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Citations (4)
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JP2003231640A (ja) * | 2002-02-04 | 2003-08-19 | Unitika Ltd | アトピー性皮膚炎治療剤 |
JP2008107275A (ja) * | 2006-10-27 | 2008-05-08 | Juntendo | アレルギー性皮膚炎の診断法 |
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WO2016035804A1 (ja) * | 2014-09-02 | 2016-03-10 | 東レ株式会社 | 掻痒性皮膚疾患の治療又は予防剤 |
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JP2003231640A (ja) * | 2002-02-04 | 2003-08-19 | Unitika Ltd | アトピー性皮膚炎治療剤 |
JP2008107275A (ja) * | 2006-10-27 | 2008-05-08 | Juntendo | アレルギー性皮膚炎の診断法 |
JP2011111416A (ja) * | 2009-11-27 | 2011-06-09 | Kao Corp | セマフォリン発現増強剤 |
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