Nuclear factor-κB p65 subunit determines the fate of aging epithelial cells
Nuclear factor (NF)-κB signaling is not only important for the immune and inflammatory responses but also for the normal development of epithelial cells, such as those in the skin and tooth. Here, we generated epithelial cell-specific p65-deficient (p65Δepi−/−) mice to analyze the roles of NF-κB sig...
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Veröffentlicht in: | Biochemical and biophysical research communications 2024-08, Vol.722, p.150143, Article 150143 |
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description | Nuclear factor (NF)-κB signaling is not only important for the immune and inflammatory responses but also for the normal development of epithelial cells, such as those in the skin and tooth. Here, we generated epithelial cell-specific p65-deficient (p65Δepi−/−) mice to analyze the roles of NF-κB signaling in epithelial cell developent. Notably, p65Δepi−/− mice exhibited no abnormalities in their appearance compared to the control (p65flox/flox) littermates. Furthermore, no major changes were observed in the skin, hair growth, and shape and color of the incisors and molars. However, 65 % of p65Δepi−/− mice exhibited corneal thickening after 8 weeks of age, and 30 % of p65Δepi−/− mice exhibited hair growth from the mandibular incisors around 24 weeks of age. No hair growth was observed at 36 and 42 weeks of age. However, micro-computed tomography images revealed a large cavity below the mandibular incisors extending to the root of the incisor. Histological analysis revealed that the cavity was occupied by a connective tissue containing hair-like structures with many dark brown granules that disappeared after melanin bleaching, confirming the presence of hair. Although inflammatory cells were also observed near the eruption site of the incisor teeth of p65Δepi−/− mice, no major disturbance was observed in the arrangement of enamel epithelial cells. Overall, these results highlight the role of p65 in the maintenance of epithelial cell homeostasis during aging.
•Epithelial-specific p65-deficient (p65Δepi−/−) mice grew without any abnormalities.•Corneal thickening and plaque formation occurred with aging.•Hair growth was observed on the labial side of lower incisors from ∼24 weeks of age.•p65 contributed to the maintenance of epithelial cell homeostasis during aging. |
doi_str_mv | 10.1016/j.bbrc.2024.150143 |
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•Epithelial-specific p65-deficient (p65Δepi−/−) mice grew without any abnormalities.•Corneal thickening and plaque formation occurred with aging.•Hair growth was observed on the labial side of lower incisors from ∼24 weeks of age.•p65 contributed to the maintenance of epithelial cell homeostasis during aging.</description><identifier>ISSN: 0006-291X</identifier><identifier>ISSN: 1090-2104</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2024.150143</identifier><identifier>PMID: 38795451</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aging - metabolism ; Animals ; Cellular Senescence ; Corneal cell ; Epithelial cell ; Epithelial Cells - cytology ; Epithelial Cells - metabolism ; Hair growth ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; NF-κB ; p65 ; Signal Transduction ; Transcription Factor RelA - genetics ; Transcription Factor RelA - metabolism</subject><ispartof>Biochemical and biophysical research communications, 2024-08, Vol.722, p.150143, Article 150143</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c222t-e33a10be1869913c11ca47544599fbde34b2d5a4faafde9d7a3e307e8504bc033</cites><orcidid>0000-0003-3616-5299 ; 0000-0002-5219-2652</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X2400679X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38795451$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Tian</creatorcontrib><creatorcontrib>Kawabata, Yuko</creatorcontrib><creatorcontrib>Kiyoshima, Tamotsu</creatorcontrib><creatorcontrib>Jimi, Eijiro</creatorcontrib><title>Nuclear factor-κB p65 subunit determines the fate of aging epithelial cells</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Nuclear factor (NF)-κB signaling is not only important for the immune and inflammatory responses but also for the normal development of epithelial cells, such as those in the skin and tooth. Here, we generated epithelial cell-specific p65-deficient (p65Δepi−/−) mice to analyze the roles of NF-κB signaling in epithelial cell developent. Notably, p65Δepi−/− mice exhibited no abnormalities in their appearance compared to the control (p65flox/flox) littermates. Furthermore, no major changes were observed in the skin, hair growth, and shape and color of the incisors and molars. However, 65 % of p65Δepi−/− mice exhibited corneal thickening after 8 weeks of age, and 30 % of p65Δepi−/− mice exhibited hair growth from the mandibular incisors around 24 weeks of age. No hair growth was observed at 36 and 42 weeks of age. However, micro-computed tomography images revealed a large cavity below the mandibular incisors extending to the root of the incisor. Histological analysis revealed that the cavity was occupied by a connective tissue containing hair-like structures with many dark brown granules that disappeared after melanin bleaching, confirming the presence of hair. Although inflammatory cells were also observed near the eruption site of the incisor teeth of p65Δepi−/− mice, no major disturbance was observed in the arrangement of enamel epithelial cells. Overall, these results highlight the role of p65 in the maintenance of epithelial cell homeostasis during aging.
•Epithelial-specific p65-deficient (p65Δepi−/−) mice grew without any abnormalities.•Corneal thickening and plaque formation occurred with aging.•Hair growth was observed on the labial side of lower incisors from ∼24 weeks of age.•p65 contributed to the maintenance of epithelial cell homeostasis during aging.</description><subject>Aging - metabolism</subject><subject>Animals</subject><subject>Cellular Senescence</subject><subject>Corneal cell</subject><subject>Epithelial cell</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - metabolism</subject><subject>Hair growth</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>NF-κB</subject><subject>p65</subject><subject>Signal Transduction</subject><subject>Transcription Factor RelA - genetics</subject><subject>Transcription Factor RelA - metabolism</subject><issn>0006-291X</issn><issn>1090-2104</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoun78AQ-So5euM0nabsCLLn7BohcFbyFNp5ql265JK_jX_BH-JltWPXoaGJ73ZeZh7BhhioDZ2XJaFMFNBQg1xRRQyS02QdCQCAS1zSYAkCVC4_Me249xCYCoMr3L9uQs16lKccIW972ryQZeWde1Ifn6vOTrLOWxL_rGd7ykjsLKNxR590oD1RFvK25ffPPCae2HZe1tzR3VdTxkO5WtIx39zAP2dH31OL9NFg83d_OLReKEEF1CUlqEgnCWaY3SITqr8lSpVOuqKEmqQpSpVZW1VUm6zK0kCTnNUlCFAykP2Ommdx3at55iZ1Y-jhfYhto-GgkZ5GpsH1CxQV1oYwxUmXXwKxs-DIIZLZqlGS2a0aLZWBxCJz_9fbGi8i_yq20AzjcADV--ewomOk-No9IHcp0pW_9f_zdZYYMh</recordid><startdate>20240830</startdate><enddate>20240830</enddate><creator>Gao, Tian</creator><creator>Kawabata, Yuko</creator><creator>Kiyoshima, Tamotsu</creator><creator>Jimi, Eijiro</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>7X8</scope><orcidid>https://orcid.org/0000-0003-3616-5299</orcidid><orcidid>https://orcid.org/0000-0002-5219-2652</orcidid></search><sort><creationdate>20240830</creationdate><title>Nuclear factor-κB p65 subunit determines the fate of aging epithelial cells</title><author>Gao, Tian ; Kawabata, Yuko ; Kiyoshima, Tamotsu ; Jimi, Eijiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c222t-e33a10be1869913c11ca47544599fbde34b2d5a4faafde9d7a3e307e8504bc033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aging - metabolism</topic><topic>Animals</topic><topic>Cellular Senescence</topic><topic>Corneal cell</topic><topic>Epithelial cell</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - metabolism</topic><topic>Hair growth</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>NF-κB</topic><topic>p65</topic><topic>Signal Transduction</topic><topic>Transcription Factor RelA - genetics</topic><topic>Transcription Factor RelA - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Tian</creatorcontrib><creatorcontrib>Kawabata, Yuko</creatorcontrib><creatorcontrib>Kiyoshima, Tamotsu</creatorcontrib><creatorcontrib>Jimi, Eijiro</creatorcontrib><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>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Tian</au><au>Kawabata, Yuko</au><au>Kiyoshima, Tamotsu</au><au>Jimi, Eijiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nuclear factor-κB p65 subunit determines the fate of aging epithelial cells</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2024-08-30</date><risdate>2024</risdate><volume>722</volume><spage>150143</spage><pages>150143-</pages><artnum>150143</artnum><issn>0006-291X</issn><issn>1090-2104</issn><eissn>1090-2104</eissn><abstract>Nuclear factor (NF)-κB signaling is not only important for the immune and inflammatory responses but also for the normal development of epithelial cells, such as those in the skin and tooth. Here, we generated epithelial cell-specific p65-deficient (p65Δepi−/−) mice to analyze the roles of NF-κB signaling in epithelial cell developent. Notably, p65Δepi−/− mice exhibited no abnormalities in their appearance compared to the control (p65flox/flox) littermates. Furthermore, no major changes were observed in the skin, hair growth, and shape and color of the incisors and molars. However, 65 % of p65Δepi−/− mice exhibited corneal thickening after 8 weeks of age, and 30 % of p65Δepi−/− mice exhibited hair growth from the mandibular incisors around 24 weeks of age. No hair growth was observed at 36 and 42 weeks of age. However, micro-computed tomography images revealed a large cavity below the mandibular incisors extending to the root of the incisor. Histological analysis revealed that the cavity was occupied by a connective tissue containing hair-like structures with many dark brown granules that disappeared after melanin bleaching, confirming the presence of hair. Although inflammatory cells were also observed near the eruption site of the incisor teeth of p65Δepi−/− mice, no major disturbance was observed in the arrangement of enamel epithelial cells. Overall, these results highlight the role of p65 in the maintenance of epithelial cell homeostasis during aging.
•Epithelial-specific p65-deficient (p65Δepi−/−) mice grew without any abnormalities.•Corneal thickening and plaque formation occurred with aging.•Hair growth was observed on the labial side of lower incisors from ∼24 weeks of age.•p65 contributed to the maintenance of epithelial cell homeostasis during aging.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38795451</pmid><doi>10.1016/j.bbrc.2024.150143</doi><orcidid>https://orcid.org/0000-0003-3616-5299</orcidid><orcidid>https://orcid.org/0000-0002-5219-2652</orcidid></addata></record> |
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subjects | Aging - metabolism Animals Cellular Senescence Corneal cell Epithelial cell Epithelial Cells - cytology Epithelial Cells - metabolism Hair growth Mice Mice, Inbred C57BL Mice, Knockout NF-κB p65 Signal Transduction Transcription Factor RelA - genetics Transcription Factor RelA - metabolism |
title | Nuclear factor-κB p65 subunit determines the fate of aging epithelial cells |
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