Protein Kinase C Is Involved in the Regulation of hairless mRNA Expression during Mouse Keratinocyte Differentiation

The hairless (hr) gene is a putative transcriptional factor whose mutations lead to hair loss in animals and humans. As a step toward understanding the role of the hr gene, we investigated the expression of hr mRNA in mouse keratinocyte differentiation. Treatment of mouse primary keratinocyte cultur...

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Veröffentlicht in:Biochemical and biophysical research communications 2001-06, Vol.284 (1), p.99-105
Hauptverfasser: Wan, Xiaozhu, Kong, Juan, Li, Yan Chun
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Kong, Juan
Li, Yan Chun
description The hairless (hr) gene is a putative transcriptional factor whose mutations lead to hair loss in animals and humans. As a step toward understanding the role of the hr gene, we investigated the expression of hr mRNA in mouse keratinocyte differentiation. Treatment of mouse primary keratinocyte cultures with phorbol-12-myristate-13-acetate (PMA) reduced DNA synthesis and sequentially induced an up-regulation of p21Cip1/WAF1 (p21), hr and involucrin (inv) mRNAs in a time-dependent fashion, suggesting that an increase in hr gene expression is associated with keratinocyte differentiation. This up-regulation was blocked by the RNA synthesis inhibitor actinomycin D. However, an increase in hr mRNA, but not in inv mRNA, was seen in cells treated with the protein synthesis inhibitor cycloheximide, suggesting that new protein synthesis is involved in the suppression of hr transcription or in the degradation of hr mRNA in the steady state. The up-regulation of hr mRNA expression by PMA was blocked by the protein kinase C (PKC) inhibitor, GF109203X. These data indicate that PKC activation is involved in the up-regulation of hr mRNA expression during mouse keratinocyte differentiation.
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As a step toward understanding the role of the hr gene, we investigated the expression of hr mRNA in mouse keratinocyte differentiation. Treatment of mouse primary keratinocyte cultures with phorbol-12-myristate-13-acetate (PMA) reduced DNA synthesis and sequentially induced an up-regulation of p21Cip1/WAF1 (p21), hr and involucrin (inv) mRNAs in a time-dependent fashion, suggesting that an increase in hr gene expression is associated with keratinocyte differentiation. This up-regulation was blocked by the RNA synthesis inhibitor actinomycin D. However, an increase in hr mRNA, but not in inv mRNA, was seen in cells treated with the protein synthesis inhibitor cycloheximide, suggesting that new protein synthesis is involved in the suppression of hr transcription or in the degradation of hr mRNA in the steady state. The up-regulation of hr mRNA expression by PMA was blocked by the protein kinase C (PKC) inhibitor, GF109203X. 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As a step toward understanding the role of the hr gene, we investigated the expression of hr mRNA in mouse keratinocyte differentiation. Treatment of mouse primary keratinocyte cultures with phorbol-12-myristate-13-acetate (PMA) reduced DNA synthesis and sequentially induced an up-regulation of p21Cip1/WAF1 (p21), hr and involucrin (inv) mRNAs in a time-dependent fashion, suggesting that an increase in hr gene expression is associated with keratinocyte differentiation. This up-regulation was blocked by the RNA synthesis inhibitor actinomycin D. However, an increase in hr mRNA, but not in inv mRNA, was seen in cells treated with the protein synthesis inhibitor cycloheximide, suggesting that new protein synthesis is involved in the suppression of hr transcription or in the degradation of hr mRNA in the steady state. The up-regulation of hr mRNA expression by PMA was blocked by the protein kinase C (PKC) inhibitor, GF109203X. These data indicate that PKC activation is involved in the up-regulation of hr mRNA expression during mouse keratinocyte differentiation.</description><subject>Animals</subject><subject>Cell Differentiation - physiology</subject><subject>Cells, Cultured</subject><subject>Cyclin-Dependent Kinase Inhibitor p21</subject><subject>Cyclins - genetics</subject><subject>Cyclins - metabolism</subject><subject>cycloheximide</subject><subject>DNA - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Enzyme Activators - pharmacology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Gene Expression Regulation</subject><subject>GF109203X</subject><subject>hairless gene</subject><subject>hr gene</subject><subject>involucrin</subject><subject>keratinocytes</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - drug effects</subject><subject>Keratinocytes - metabolism</subject><subject>Mice</subject><subject>phorbol ester</subject><subject>protein kinase C</subject><subject>Protein Kinase C - antagonists &amp; inhibitors</subject><subject>Protein Kinase C - metabolism</subject><subject>Protein Precursors - genetics</subject><subject>Protein Precursors - metabolism</subject><subject>Protein Synthesis Inhibitors - pharmacology</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>Transcription Factors</subject><subject>Up-Regulation</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtv3CAURlGVqpkk3XZZscrOUy7GD5bR5DVK-lCUSt0hjK8TKg9MAI-afx_cGamrrtDlnu8IPkI-AVsCY_WXrgtmyRmDpZC8fEcWwCQrODBxRBYsEwWX8OuYnMT4O1MgavmBHAOUjWibZkHSj-ATWkfvrNMR6YquI127nR932NN8n56RPuDTNOpkvaN-oM_ahhFjpJuHbxf06s825GHe9VOw7ol-9VMW3WHICefNa0J6aYcBA7pk_1rOyPtBjxE_Hs5T8vP66nF1W9x_v1mvLu4LUzaQirIDbhrd6lpLUSOUktdVq1kjmqoasOe8GloOssJykK0ELkAw04lOy5rpXpen5Hzv3Qb_MmFMamOjwXHUDvMjFTRziosMLvegCT7GgIPaBrvR4VUBU3PPau5ZzT2ruecc-HwwT90G-3_4odgMtHsA8_92FoOKxqIz2NuAJqne2_-53wBxMYzB</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Wan, Xiaozhu</creator><creator>Kong, Juan</creator><creator>Li, Yan Chun</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope></search><sort><creationdate>20010601</creationdate><title>Protein Kinase C Is Involved in the Regulation of hairless mRNA Expression during Mouse Keratinocyte Differentiation</title><author>Wan, Xiaozhu ; Kong, Juan ; Li, Yan Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-3b12c7a8a6a946e1392658a074755fed225f82195e3f989124140cb4ba960ada3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Cell Differentiation - physiology</topic><topic>Cells, Cultured</topic><topic>Cyclin-Dependent Kinase Inhibitor p21</topic><topic>Cyclins - genetics</topic><topic>Cyclins - metabolism</topic><topic>cycloheximide</topic><topic>DNA - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Enzyme Activators - pharmacology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Gene Expression Regulation</topic><topic>GF109203X</topic><topic>hairless gene</topic><topic>hr gene</topic><topic>involucrin</topic><topic>keratinocytes</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - drug effects</topic><topic>Keratinocytes - metabolism</topic><topic>Mice</topic><topic>phorbol ester</topic><topic>protein kinase C</topic><topic>Protein Kinase C - antagonists &amp; inhibitors</topic><topic>Protein Kinase C - metabolism</topic><topic>Protein Precursors - genetics</topic><topic>Protein Precursors - metabolism</topic><topic>Protein Synthesis Inhibitors - pharmacology</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>Transcription Factors</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wan, Xiaozhu</creatorcontrib><creatorcontrib>Kong, Juan</creatorcontrib><creatorcontrib>Li, Yan Chun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wan, Xiaozhu</au><au>Kong, Juan</au><au>Li, Yan Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protein Kinase C Is Involved in the Regulation of hairless mRNA Expression during Mouse Keratinocyte Differentiation</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>284</volume><issue>1</issue><spage>99</spage><epage>105</epage><pages>99-105</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>The hairless (hr) gene is a putative transcriptional factor whose mutations lead to hair loss in animals and humans. As a step toward understanding the role of the hr gene, we investigated the expression of hr mRNA in mouse keratinocyte differentiation. Treatment of mouse primary keratinocyte cultures with phorbol-12-myristate-13-acetate (PMA) reduced DNA synthesis and sequentially induced an up-regulation of p21Cip1/WAF1 (p21), hr and involucrin (inv) mRNAs in a time-dependent fashion, suggesting that an increase in hr gene expression is associated with keratinocyte differentiation. This up-regulation was blocked by the RNA synthesis inhibitor actinomycin D. However, an increase in hr mRNA, but not in inv mRNA, was seen in cells treated with the protein synthesis inhibitor cycloheximide, suggesting that new protein synthesis is involved in the suppression of hr transcription or in the degradation of hr mRNA in the steady state. The up-regulation of hr mRNA expression by PMA was blocked by the protein kinase C (PKC) inhibitor, GF109203X. These data indicate that PKC activation is involved in the up-regulation of hr mRNA expression during mouse keratinocyte differentiation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11374877</pmid><doi>10.1006/bbrc.2001.4923</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Cell Differentiation - physiology
Cells, Cultured
Cyclin-Dependent Kinase Inhibitor p21
Cyclins - genetics
Cyclins - metabolism
cycloheximide
DNA - metabolism
Dose-Response Relationship, Drug
Enzyme Activators - pharmacology
Enzyme Inhibitors - pharmacology
Gene Expression Regulation
GF109203X
hairless gene
hr gene
involucrin
keratinocytes
Keratinocytes - cytology
Keratinocytes - drug effects
Keratinocytes - metabolism
Mice
phorbol ester
protein kinase C
Protein Kinase C - antagonists & inhibitors
Protein Kinase C - metabolism
Protein Precursors - genetics
Protein Precursors - metabolism
Protein Synthesis Inhibitors - pharmacology
Proteins - genetics
Proteins - metabolism
RNA, Messenger - metabolism
Tetradecanoylphorbol Acetate - pharmacology
Transcription Factors
Up-Regulation
title Protein Kinase C Is Involved in the Regulation of hairless mRNA Expression during Mouse Keratinocyte Differentiation
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