Dynamic expression patterns of tenascin, proteoglycans, and cell adhesion molecules during human hair follicle morphogenesis

The development of skin appendages such as hair, feathers, and teeth is brought about by reciprocal interactions between epidermal and mesenchymal tissues and is thought to be influenced in part by cell adhesion molecules and components of the extracellular matrix. The developmental distributions of...

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Veröffentlicht in:Developmental dynamics 1994-02, Vol.199 (2), p.141-155
Hauptverfasser: Kaplan, Elizabeth D., Holbrook, Karen A.
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description The development of skin appendages such as hair, feathers, and teeth is brought about by reciprocal interactions between epidermal and mesenchymal tissues and is thought to be influenced in part by cell adhesion molecules and components of the extracellular matrix. The developmental distributions of tenascin, neural cell adhesion molecule (NCAM), E‐cadherin, intercellular adhesion molecule 1 (ICAM‐1), chondroitin sulfate proteoglycan (CSPG), and the heparan sulfate proteoglycan perlecan were studied in relation to hair follicle morphogenesis in fetal human skin. Tenascin first appeared in developing skin in focal concentrations at the epidermal‐mesenchymal interface, just prior to, and presumably correlated with, hair follicle initiation. Tenascin immunostaining remained prominent in the basement membrane zone and extracellular matrix of the follicle sheath during subsequent morphogenetic stages. Two forms of tenascin (Mr 250 × 103 and 280–300 × 103), were revealed by Western blots of skin extracts. NCAM immunolabeling was initially present throughout the dermis, and became progressively restricted to the dermal condensation and the follicle sheath. Western blot analysis revealed an isoform of NCAM (Mr 160 × 103) which lacked polysialic acid. At all stages, E‐cadherin staining was diminished on follicle cells situated adjacent to the basement membrane, relative to cells in the follicle interior. Follicle‐specific immunostaining for ICAM‐1 was transient, appearing only at the pre‐germ and hair germ stages of development. Antibodies to three distinct CSPG determinants revealed unique immunolabeling patterns following follicle initiation: One CSPG epitope co‐distributed with tenascin in the follicle basement membrane and follicle sheath extracellular matrix; one CSPG epitope was similarly expressed, and was also found on follicle epithelial cells; and the third CSPG determinant was noticeably absent from the follicle sheath during elongation of the developing appendage. Perlecan was concentrated in the dermal papilla, in addition to its distribution in all skin basement membranes. A model for how these diverse molecules may inter/act to influence human hair follicle morphogenesis is presented. © 1994 Wiley‐Liss, Inc.
doi_str_mv 10.1002/aja.1001990207
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The developmental distributions of tenascin, neural cell adhesion molecule (NCAM), E‐cadherin, intercellular adhesion molecule 1 (ICAM‐1), chondroitin sulfate proteoglycan (CSPG), and the heparan sulfate proteoglycan perlecan were studied in relation to hair follicle morphogenesis in fetal human skin. Tenascin first appeared in developing skin in focal concentrations at the epidermal‐mesenchymal interface, just prior to, and presumably correlated with, hair follicle initiation. Tenascin immunostaining remained prominent in the basement membrane zone and extracellular matrix of the follicle sheath during subsequent morphogenetic stages. Two forms of tenascin (Mr 250 × 103 and 280–300 × 103), were revealed by Western blots of skin extracts. NCAM immunolabeling was initially present throughout the dermis, and became progressively restricted to the dermal condensation and the follicle sheath. Western blot analysis revealed an isoform of NCAM (Mr 160 × 103) which lacked polysialic acid. At all stages, E‐cadherin staining was diminished on follicle cells situated adjacent to the basement membrane, relative to cells in the follicle interior. Follicle‐specific immunostaining for ICAM‐1 was transient, appearing only at the pre‐germ and hair germ stages of development. Antibodies to three distinct CSPG determinants revealed unique immunolabeling patterns following follicle initiation: One CSPG epitope co‐distributed with tenascin in the follicle basement membrane and follicle sheath extracellular matrix; one CSPG epitope was similarly expressed, and was also found on follicle epithelial cells; and the third CSPG determinant was noticeably absent from the follicle sheath during elongation of the developing appendage. Perlecan was concentrated in the dermal papilla, in addition to its distribution in all skin basement membranes. A model for how these diverse molecules may inter/act to influence human hair follicle morphogenesis is presented. © 1994 Wiley‐Liss, Inc.</description><identifier>ISSN: 1058-8388</identifier><identifier>EISSN: 1097-0177</identifier><identifier>DOI: 10.1002/aja.1001990207</identifier><identifier>PMID: 7515726</identifier><identifier>CODEN: DEDYEI</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Blotting, Western ; Cadherins - analysis ; Cell Adhesion Molecules - analysis ; Cell Adhesion Molecules, Neuronal - analysis ; Cell Differentiation - physiology ; Chondroitin Sulfates - analysis ; Electrophoresis, Polyacrylamide Gel ; Embryology: invertebrates and vertebrates. Teratology ; Embryonic and Fetal Development - physiology ; Extracellular matrix ; Extracellular Matrix Proteins - analysis ; E‐cadherin ; Fundamental and applied biological sciences. Psychology ; Gestational Age ; Hair - chemistry ; Hair - cytology ; Hair - embryology ; Hair follicle morphogenesis ; Human ; Humans ; ICAM‐1 ; Immunohistochemistry ; Intercellular Adhesion Molecule-1 ; Morphogenesis - physiology ; NCAM ; Organogenesis. Fetal development ; Organogenesis. 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The developmental distributions of tenascin, neural cell adhesion molecule (NCAM), E‐cadherin, intercellular adhesion molecule 1 (ICAM‐1), chondroitin sulfate proteoglycan (CSPG), and the heparan sulfate proteoglycan perlecan were studied in relation to hair follicle morphogenesis in fetal human skin. Tenascin first appeared in developing skin in focal concentrations at the epidermal‐mesenchymal interface, just prior to, and presumably correlated with, hair follicle initiation. Tenascin immunostaining remained prominent in the basement membrane zone and extracellular matrix of the follicle sheath during subsequent morphogenetic stages. Two forms of tenascin (Mr 250 × 103 and 280–300 × 103), were revealed by Western blots of skin extracts. NCAM immunolabeling was initially present throughout the dermis, and became progressively restricted to the dermal condensation and the follicle sheath. Western blot analysis revealed an isoform of NCAM (Mr 160 × 103) which lacked polysialic acid. At all stages, E‐cadherin staining was diminished on follicle cells situated adjacent to the basement membrane, relative to cells in the follicle interior. Follicle‐specific immunostaining for ICAM‐1 was transient, appearing only at the pre‐germ and hair germ stages of development. Antibodies to three distinct CSPG determinants revealed unique immunolabeling patterns following follicle initiation: One CSPG epitope co‐distributed with tenascin in the follicle basement membrane and follicle sheath extracellular matrix; one CSPG epitope was similarly expressed, and was also found on follicle epithelial cells; and the third CSPG determinant was noticeably absent from the follicle sheath during elongation of the developing appendage. Perlecan was concentrated in the dermal papilla, in addition to its distribution in all skin basement membranes. A model for how these diverse molecules may inter/act to influence human hair follicle morphogenesis is presented. © 1994 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Cadherins - analysis</subject><subject>Cell Adhesion Molecules - analysis</subject><subject>Cell Adhesion Molecules, Neuronal - analysis</subject><subject>Cell Differentiation - physiology</subject><subject>Chondroitin Sulfates - analysis</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Embryonic and Fetal Development - physiology</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix Proteins - analysis</subject><subject>E‐cadherin</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gestational Age</subject><subject>Hair - chemistry</subject><subject>Hair - cytology</subject><subject>Hair - embryology</subject><subject>Hair follicle morphogenesis</subject><subject>Human</subject><subject>Humans</subject><subject>ICAM‐1</subject><subject>Immunohistochemistry</subject><subject>Intercellular Adhesion Molecule-1</subject><subject>Morphogenesis - physiology</subject><subject>NCAM</subject><subject>Organogenesis. Fetal development</subject><subject>Organogenesis. Physiological fonctions</subject><subject>Perlecan</subject><subject>Proteoglycans - analysis</subject><subject>Tenascin</subject><issn>1058-8388</issn><issn>1097-0177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi0EKm3hyg3JB8SpW-w4ydjHVaF8qBIXOEezzmTXlWMHO1FZiR-Pl10Vbpw80jzveOZh7JUU11KI6h3e46GQxohKwBN2LoWBlZAATw91o1daaf2cXeR8L4TQbS3P2Bk0soGqPWe_3u8Djs5y-jklytnFwCecZ0oh8zjwmQJm68IVn1KcKW793mLIVxxDzy15z7Hf0Z_YGD3ZxVPm_ZJc2PLdMmLgO3SJD9F7Zz0VKE27uKVQMvkFezagz_Ty9F6y77cfvt18Wt19_fj5Zn23sqotxxBW1tgWFEBjwOq6RkV9DY0GM0iB1aZqe6lU09tKqwplrS1K2gw11NIMoC7Z2-PccsOPhfLcjS4flsdAcckdtI0E0bYFvD6CNsWcEw3dlNyIad9J0R10d0V391d3Cbw-TV42I_WP-Mlv6b859YtF9EPCYF1-xJTR0ChdMHPEHpyn_X8-7dZf1v-s8BulAppf</recordid><startdate>199402</startdate><enddate>199402</enddate><creator>Kaplan, Elizabeth D.</creator><creator>Holbrook, Karen A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>199402</creationdate><title>Dynamic expression patterns of tenascin, proteoglycans, and cell adhesion molecules during human hair follicle morphogenesis</title><author>Kaplan, Elizabeth D. ; Holbrook, Karen A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3697-ea2c9c67377597c844a3ed475879f10a2b26d1335dc2832a148ca1ebf47419f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Cadherins - analysis</topic><topic>Cell Adhesion Molecules - analysis</topic><topic>Cell Adhesion Molecules, Neuronal - analysis</topic><topic>Cell Differentiation - physiology</topic><topic>Chondroitin Sulfates - analysis</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Embryonic and Fetal Development - physiology</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix Proteins - analysis</topic><topic>E‐cadherin</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gestational Age</topic><topic>Hair - chemistry</topic><topic>Hair - cytology</topic><topic>Hair - embryology</topic><topic>Hair follicle morphogenesis</topic><topic>Human</topic><topic>Humans</topic><topic>ICAM‐1</topic><topic>Immunohistochemistry</topic><topic>Intercellular Adhesion Molecule-1</topic><topic>Morphogenesis - physiology</topic><topic>NCAM</topic><topic>Organogenesis. Fetal development</topic><topic>Organogenesis. Physiological fonctions</topic><topic>Perlecan</topic><topic>Proteoglycans - analysis</topic><topic>Tenascin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaplan, Elizabeth D.</creatorcontrib><creatorcontrib>Holbrook, Karen A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaplan, Elizabeth D.</au><au>Holbrook, Karen A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamic expression patterns of tenascin, proteoglycans, and cell adhesion molecules during human hair follicle morphogenesis</atitle><jtitle>Developmental dynamics</jtitle><addtitle>Dev Dyn</addtitle><date>1994-02</date><risdate>1994</risdate><volume>199</volume><issue>2</issue><spage>141</spage><epage>155</epage><pages>141-155</pages><issn>1058-8388</issn><eissn>1097-0177</eissn><coden>DEDYEI</coden><abstract>The development of skin appendages such as hair, feathers, and teeth is brought about by reciprocal interactions between epidermal and mesenchymal tissues and is thought to be influenced in part by cell adhesion molecules and components of the extracellular matrix. The developmental distributions of tenascin, neural cell adhesion molecule (NCAM), E‐cadherin, intercellular adhesion molecule 1 (ICAM‐1), chondroitin sulfate proteoglycan (CSPG), and the heparan sulfate proteoglycan perlecan were studied in relation to hair follicle morphogenesis in fetal human skin. Tenascin first appeared in developing skin in focal concentrations at the epidermal‐mesenchymal interface, just prior to, and presumably correlated with, hair follicle initiation. Tenascin immunostaining remained prominent in the basement membrane zone and extracellular matrix of the follicle sheath during subsequent morphogenetic stages. Two forms of tenascin (Mr 250 × 103 and 280–300 × 103), were revealed by Western blots of skin extracts. NCAM immunolabeling was initially present throughout the dermis, and became progressively restricted to the dermal condensation and the follicle sheath. Western blot analysis revealed an isoform of NCAM (Mr 160 × 103) which lacked polysialic acid. At all stages, E‐cadherin staining was diminished on follicle cells situated adjacent to the basement membrane, relative to cells in the follicle interior. Follicle‐specific immunostaining for ICAM‐1 was transient, appearing only at the pre‐germ and hair germ stages of development. Antibodies to three distinct CSPG determinants revealed unique immunolabeling patterns following follicle initiation: One CSPG epitope co‐distributed with tenascin in the follicle basement membrane and follicle sheath extracellular matrix; one CSPG epitope was similarly expressed, and was also found on follicle epithelial cells; and the third CSPG determinant was noticeably absent from the follicle sheath during elongation of the developing appendage. Perlecan was concentrated in the dermal papilla, in addition to its distribution in all skin basement membranes. A model for how these diverse molecules may inter/act to influence human hair follicle morphogenesis is presented. © 1994 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7515726</pmid><doi>10.1002/aja.1001990207</doi><tpages>15</tpages></addata></record>
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ispartof Developmental dynamics, 1994-02, Vol.199 (2), p.141-155
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subjects Biological and medical sciences
Blotting, Western
Cadherins - analysis
Cell Adhesion Molecules - analysis
Cell Adhesion Molecules, Neuronal - analysis
Cell Differentiation - physiology
Chondroitin Sulfates - analysis
Electrophoresis, Polyacrylamide Gel
Embryology: invertebrates and vertebrates. Teratology
Embryonic and Fetal Development - physiology
Extracellular matrix
Extracellular Matrix Proteins - analysis
E‐cadherin
Fundamental and applied biological sciences. Psychology
Gestational Age
Hair - chemistry
Hair - cytology
Hair - embryology
Hair follicle morphogenesis
Human
Humans
ICAM‐1
Immunohistochemistry
Intercellular Adhesion Molecule-1
Morphogenesis - physiology
NCAM
Organogenesis. Fetal development
Organogenesis. Physiological fonctions
Perlecan
Proteoglycans - analysis
Tenascin
title Dynamic expression patterns of tenascin, proteoglycans, and cell adhesion molecules during human hair follicle morphogenesis
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