Literature DB >> 16871359

Effects of bio-active ceramic resources in cutaneous wound healing and the role of TGF-beta signaling.

Jae-Yong Chung1, Sun Hee Do, Won-Il Jeong, Da-Hee Jeong, Sang-Joon Park, Mi-Ran Ki, Dong-Mi Kwak, Soon-Bok Kim, Myung-Sook Choi, Kyu-Shik Jeong.   

Abstract

The wound healing process is a highly orchestrated process, which includes inflammation, re-epithelialization, granulation tissue formation, matrix formation and re-modeling. In this paper, we attempt to determine if bio-active ceramic resource powder particles had an effect on cutaneous wound healing. Furthermore, we investigated its related mechanism and the expression of Smads of cutaneous wound healing, which can be accelerated by bio-active ceramic ointment. Topically applied lesions of 5%, 10% and 15% bio-active ceramic ointment (AO) showed accelerated wound closure, re-epithelialization, and the related immediate down stream of TGF-beta (p-Smad2/3 and Smad3) was suppressed. In particular, 10% and 15% AO lesions became closed faster at Days 3 and 4 of post-wound and p-Smad2/3 was also suppressed. All AO lesions showed accelerated mild wound closure at Day 6, but there were no significant difference. Several papers reported that Smad3 may mediate the signaling pathways that is inhibitory to wound healing, as the deletion of Smad3 leads to enhanced re-epithelialization and contraction of the wound area. This study showed that topical, bio-active ceramic ointment applications accelerated wound closure, re-epithelialization and the suppression of Smad proteins (p-Smad2/3, Smad3). The data revealed that the suppression of Smad3, which was induced by bio-active ceramic resources powder particles affected re-epithelialization and cutaneous wound closure. At the end of this paper, we concluded that bio-active ceramic resources affect cutaneous wound healing by accelerating the re-epithelialization of keratinocytes and that is mediated by the suppression of related protein, Smad3.

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Year:  2006        PMID: 16871359     DOI: 10.1007/s11010-006-9283-7

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  31 in total

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Journal:  N Engl J Med       Date:  1999-09-02       Impact factor: 91.245

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Journal:  Science       Date:  1999-02-26       Impact factor: 47.728

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Journal:  J Immunol       Date:  2006-05-01       Impact factor: 5.422

Review 4.  Smads: transcriptional activators of TGF-beta responses.

Authors:  R Derynck; Y Zhang; X H Feng
Journal:  Cell       Date:  1998-12-11       Impact factor: 41.582

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Journal:  Lab Invest       Date:  1994-06       Impact factor: 5.662

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Journal:  Nat Cell Biol       Date:  1999-09       Impact factor: 28.824

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Authors:  Chang-Woo Lee; Won-Il Jeong; Dong-Hyung Noh; Da-Hee Jeong; Sun-Hee DO; Yoo-Kyeong Kim; Oh-Deog Kwon; Tae-Hwan Kim; Kyu-Shik Jeong
Journal:  J Vet Med Sci       Date:  2005-04       Impact factor: 1.267

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Authors:  A Igarashi; H Okochi; D M Bradham; G R Grotendorst
Journal:  Mol Biol Cell       Date:  1993-06       Impact factor: 4.138

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Authors:  F Grinnell
Journal:  J Cell Sci       Date:  1992-01       Impact factor: 5.285

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