The Therapy of Burn Wound Healing in Rat (Wistar) by Using the Combination of Peripheral Blood Mononuclear Cells (PBMCs) and Bone Marroe BM-Derived Mesenchymal Stem Cell
Downloads
The therapy to heal the bum wound is still imperfect, therefore it is important to conduct specific research concerning this topic that benefits to society. Using both Bone Marrow-stem cell (BM-MSc) and peripheral blood mononuclear cells (PBMCs) from allogenic donors as part of the therapy to heal the bum wound seems to give positive prospect for the future treatment. In this experiment, PBMC and rat BM- derived from mesenchymal stem cell were used as the therapy model. lmmunocytochemistry was used as the method to characterize the phenotype of MSc, It was also used to express the collagen type I and the Indirect ELISA in analyzing the TGF·P 1 secretion. The rats with bum wound were divided into 2 kinds of group; the first group of rats was selected to control the use of PBS; while second group of rats was used as the treatment object that was medicated by the applying of the combination of both BM-MSC and PBMC. Stem-cells subcutaneously administered dose applied to each rat was around of 2 x 106 cells. The result showed that the levels of TGF-β1 secretion in day 3rd and day 7th on the rats which were treated by using the combination of BM-MSC and PBMC were higher compared to the rats from the control group. The experiment that concerns on the thickness of the collagen showed that combination between BM-MSC and PBMC stem cell make it possible in increasing the thickness of collagen 1, besides; it also showed significant differences (p=0.000). This research proved that the combination of BM-MSC and PBMC stem cell served can accelerate the healing process for the bum wound on rats through Increasing of TGF-P 1 secretion and collagen type 1 expression, It means that PBMCs can be applied as good as chemoattractant.
Abe R, Donnely SC, Peng T, Bucala R, Metz CN. 2001. Peripheral blood fibrocytes: differentiation pathway and migration to wound sites. J. lmmunol. (166): pp. 7556-62.
Evers LH, Bhavar D, Malla.nder P. 2010. The biology of bum injury. Experi. Dermatol. (19): pp. 777-783.
Herdrich BJ, Lind RC, Liechty KW. 2008. REVIEW Multi potent adult progenitor cells: their role in wound healing and the treatment of dermal wounds. Cytotherapy10 (6): pp. 543-550.
Kumar S, Peng FW, David JL. 2004. What is new in wound healing. Turkish J. Med. Sci. (34): pp. 147-160.
Lau K, Paus R, Tiede S, Oay P, Bayat A. 2009. Exploring the role of stem cells in cutaneous wound healing. Experi. Dermatol. (18): pp. 921-933.
Liu ZJ, Zhuge Y, Velazquez OC. 2008. Trafficking and differentiation of mesenchymal stem cells. J. Cellul. Biochem. (106): pp. 984-991.
Maxson S, Lopez EA, Yoo D, Miagkova AD, Leroux MA. 2012. Concise Review: Role of mesenchymal stem cells in wound repair. Stem cells translation medicine; (1): pp. 142-149.
Medina A, Erin B, Nicholas C, Aziz G. 2009. Circulating monocytes have the capacity to be trans-differentiated into keratinocyte-like cells. Wound repair and regeneration 17, pp. 268-277 by the Wound Healing Society.
Metcalfe AD, Ferguson MWJ. 2007. Tissue engineering of replacement skin: the crossroads of biomaterials, wound healing, embryonic development, stem cells and regeneration. J. Royal Soc. Interface. (4): pp. 413-437.
Moioli EK, Clark PA, Chen M, Dennis JE, Erickson HP, Gerson SL and Mao JJ. 2008. Synergistic actions of hematopoietic and mesenchymal stem/progenitor cells in vascularizing Bioengineered Tissues. Plos One 3 (12): pp.1-11.
Newman SL, Tucci MA. 1990. Regulation of human monocyte/macrophage function by extracellular matrix adherence of monocytes to collagen matrices enhances phagocytosis of opsonized bacteria by activation of complement receptors and enhancement of Fc receptor function. J. Clin. lnvestig. 86, pp. 703-714.
Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, Mosca JD, Moorman MA, Simonetti OW, Craig S, Marshak OR. 1999. Multi-lineage potential of adult human mesenchymal stem cells. Science (284): pp. 143--147.
Sasaki M, R Abe, Y Fujita, S Ando, D lnokuma, Hiroshi Shimizu. 2008. Mesenchymal stem cells are recruited into skin cell type repair by trans-differentiation into multiple wounded skin and contribute to wound. J. lmmunol. 2008; (180): pp. 2581-2587.
Smith AN, Willis E, Chan VT, Muffley LA, lsik FF,Gibran NS, Hocking AM. 2010. Mesenchymal stem cells induce dermal fibroblast responses to injury Experimental Cell Research. January 1; 316(1 ): pp. 48-54.
Syamsuhidayat R. 1997. Buku ajar ilmu bedah. Edisi Revisi, Penerbit Buku Kedokteran EGC.Jakarta Vem AK, BA Latense. 2001. Specimen collection and analysis bum wound. Methods in molecular medicine wound healing. Edited by Luisa D & Aime LB. 78. Human Press Inc.
Totowa NJ, Yang L, Chan T, Demare J, lwashina T, Ghahary A, Scott PG, Tredget EE. 2001. Healing of Bum Wounds in Transgenic Mice Overexpressing Transforming Growth Factor-β1 in the Epidermis. Ameri. J. Pathol. 159 (6), Yang L, Qiu ex, Ludlow A Ferguson MWJ, Brunner. 1999. Technical advance active transforming growth factor-b in wound repair determination using a new assay. Am. J. Pathol. (154): pp. 10&-111.
1. As an author you (or your employer or institution) may do the following:
- make copies (print or electronic) of the article for your own personal use, including for your own classroom teaching use;
- make copies and distribute such copies (including through e-mail) of the article to research colleagues, for the personal use by such colleagues (but not commercially or systematically, e.g. via an e-mail list or list server);
- present the article at a meeting or conference and to distribute copies of the article to the delegates attending such meeting;
- for your employer, if the article is a ‘work for hire', made within the scope of your employment, your employer may use all or part of the information in the article for other intra-company use (e.g. training);
- retain patent and trademark rights and rights to any process, procedure, or article of manufacture described in the article;
- include the article in full or in part in a thesis or dissertation (provided that this is not to be published commercially);
- use the article or any part thereof in a printed compilation of your works, such as collected writings or lecture notes (subsequent to publication of the article in the journal); and prepare other derivative works, to extend the article into book-length form, or to otherwise re-use portions or excerpts in other works, with full acknowledgement of its original publication in the journal;
- may reproduce or authorize others to reproduce the article, material extracted from the article, or derivative works for the author's personal use or for company use, provided that the source and the copyright notice are indicated, the copies are not used in any way that implies JSCRTE endorsement of a product or service of any employer, and the copies themselves are not offered for sale.
All copies, print or electronic, or other use of the paper or article must include the appropriate bibliographic citation for the article's publication in the journal.
2. Requests from third parties
Although authors are permitted to re-use all or portions of the article in other works, this does not include granting third-party requests for reprinting, republishing, or other types of re-use. Requests for all uses not included above, including the authorization of third parties to reproduce or otherwise use all or part of the article (including figures and tables), should be referred to JSCRTE by going to our website at http://e-journal.unair.ac.id/index.php/JSCRTE
3. Author Online Use
- Personal Servers. Authors and/or their employers shall have the right to post the accepted version of articles pre-print version of the article, or revised personal version of the final text of the article (to reflect changes made in the peer review and editing process) on their own personal servers or the servers of their institutions or employers without permission from JSCRTE, provided that the posted version includes a prominently displayed JSCRTE copyright notice and, when published, a full citation to the original publication, including a link to the article abstract in the journal homepage. Authors shall not post the final, published versions of their papers;
- Classroom or Internal Training Use. An author is expressly permitted to post any portion of the accepted version of his/her own articles on the author's personal web site or the servers of the author's institution or company in connection with the author's teaching, training, or work responsibilities, provided that the appropriate copyright, credit, and reuse notices appear prominently with the posted material. Examples of permitted uses are lecture materials, course packs, e-reserves, conference presentations, or in-house training courses;
- Electronic Preprints. Before submitting an article to an JSCRTE, authors frequently post their manuscripts to their own web site, their employer's site, or to another server that invites constructive comment from colleagues. Upon submission of an article to JSCRTE, an author is required to transfer copyright in the article to JSCRTE, and the author must update any previously posted version of the article with a prominently displayed JSCRTE copyright notice. Upon publication of an article by the JSCRTE, the author must replace any previously posted electronic versions of the article with either (1) the full citation to the work with a Digital Object Identifier (DOI) or link to the article abstract in JSCRTE homepage, or (2) the accepted version only (not the final, published version), including the JSCRTE copyright notice and full citation, with a link to the final, published article in journal homepage.
4. Articles in Press (AiP) service
JSCRTE may choose to publish an abstract or portions of the paper before we publish it in the journal. Please contact our Production department immediately if you do not want us to make any such prior publication for any reason, including disclosure of a patentable invention.
5. Author/Employer Rights
If you are employed and prepared the article on a subject within the scope of your employment, the copyright in the article belongs to your employer as a work-for-hire. In that case, JSCRTE assumes that when you sign this Form, you are authorized to do so by your employer and that your employer has consented to the transfer of copyright, to the representation and warranty of publication rights, and to all other terms and conditions of this Form. If such authorization and consent has not been given to you, an authorized representative of your employer should sign this Form as the Author.
6. JSCRTE Copyright Ownership
It is the formal policy of JSCRTE to own the copyrights to all copyrightable material in its technical publications and to the individual contributions contained therein, in order to protect the interests of the JSCRTE, its authors and their employers, and, at the same time, to facilitate the appropriate re-use of this material by others. JSCRTE distributes its technical publications throughout the world and does so by various means such as hard copy, microfiche, microfilm, and electronic media. It also abstracts and may translate its publications, and articles contained therein, for inclusion in various compendiums, collective works, databases and similar publications
Every accepted manuscript should be accompanied by "Copyright Transfer Agreement" prior to the article publication.