Literature DB >> 28497366

Evaluation of persistence and distribution of intra-dermally administered PKH26 labelled goat bone marrow derived mesenchymal stem cells in cutaneous wound healing model.

M D Pratheesh1,2, Nitin E Gade1,3, Amar Nath1,4, Pawan K Dubey1,5, T B Sivanarayanan6, D N Madhu6, T R Sreekumar1,2, G Saikumar7, G Taru Sharma8.   

Abstract

The current study was designed to study the persistence and distribution of caprine bone marrow derived mesenchymal stem cells (cBM-MSCs) when administered intra-dermally in experimentally induced cutaneous wounds in rabbits. MSC's from goat bone marrow were isolated and their differentiation potential towards adipogenic and osteogenic lineages were assayed in vitro. The isolated cells were phenotypically analysed using flow cytometry for the expression of MSC specific matrix receptors (CD73, CD105 and Stro-1) and absence of hematopoietic lineage markers. Further, these in vitro expanded MSCs were stained with PKH26 lipophilic cell membrane red fluorescent dye and prepared for transplantation into cutaneous wounds created on rabbits. Five, 2 cm linear full thickness skin incisions were created on either side of dorsal midline of New Zealand white rabbits (n = 4). Four wounds in each animal were implanted intra-dermally with PKH26 labelled cBM-MSCs suspended in 500 µl of Phosphate Buffer Saline (PBS). Fifth wound was injected with PBS alone and treated as negative control. The skin samples were collected from respective wounds on 3, 7, 10 and 14 days after the wound creation, and cryosections of 6 µM were made from it. Fluorescent microscopy of these cryosections showed that the PKH26 labelled transplanted cells and their daughter cells demonstrated a diffuse pattern of distribution initially and were later concentrated towards the wound edges and finally appeared to be engrafted with the newly developed skin tissues. The labelled cells were found retained in the wound bed throughout the period of 14 days of experimental study with a gradual decline in their intensity of red fluorescence probably due to the dye dilution as a result of multiple cell division. The retention of transplanted MSCs within the wound bed even after the complete wound healing suggests that in addition to their paracrine actions as already been reported, they may have direct involvement in various stages of intricate wound healing process which needs to be explored further.

Entities:  

Keywords:  Bone marrow derived mesenchymal stem cells; Caprine; Cutaneous wound healing; Hair regeneration; In vivo tracking; PKH26

Year:  2017        PMID: 28497366      PMCID: PMC5660742          DOI: 10.1007/s10616-017-0097-0

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  33 in total

Review 1.  Fluorescent dyes for lymphocyte migration and proliferation studies.

Authors:  C R Parish
Journal:  Immunol Cell Biol       Date:  1999-12       Impact factor: 5.126

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3.  PKH26 can transfer to host cells in vitro and vivo.

Authors:  Peng Li; Run Zhang; Haitao Sun; Lei Chen; Fang Liu; Chen Yao; Mouxuan Du; Xiaodan Jiang
Journal:  Stem Cells Dev       Date:  2012-10-19       Impact factor: 3.272

4.  Paracrine effects of mesenchymal stem cells enhance vascular regeneration in ischemic murine skin.

Authors:  Stefan Schlosser; Cyrill Dennler; Riccardo Schweizer; Daniel Eberli; Jens V Stein; Volker Enzmann; Pietro Giovanoli; Dominique Erni; Jan A Plock
Journal:  Microvasc Res       Date:  2012-02-25       Impact factor: 3.514

5.  Human mesenchymal stem cells persist, demonstrate site-specific multipotential differentiation, and are present in sites of wound healing and tissue regeneration after transplantation into fetal sheep.

Authors:  T C Mackenzie; A W Flake
Journal:  Blood Cells Mol Dis       Date:  2001 May-Jun       Impact factor: 3.039

6.  Serial in vivo imaging of the porcine heart after percutaneous, intramyocardially injected 111In-labeled human mesenchymal stromal cells.

Authors:  Stig Lyngbaek; Rasmus S Ripa; Mandana Haack-Sørensen; Annette Cortsen; Linda Kragh; Claus B Andersen; Erik Jørgensen; Andreas Kjaer; Jens Kastrup; Birger Hesse
Journal:  Int J Cardiovasc Imaging       Date:  2009-11-18       Impact factor: 2.357

7.  The immunosuppressive effects of human bone marrow-derived mesenchymal stem cells target T cell proliferation but not its effector function.

Authors:  Rajesh Ramasamy; Chih Kong Tong; Heng Fong Seow; Sharmili Vidyadaran; Francesco Dazzi
Journal:  Cell Immunol       Date:  2008-05-27       Impact factor: 4.868

8.  A comparative study of PKH67, DiI, and BrdU labeling techniques for tracing rat mesenchymal stem cells.

Authors:  Miriam Nagyova; Lucia Slovinska; Juraj Blasko; Ivana Grulova; Maria Kuricova; Viera Cigankova; Denisa Harvanova; Dasa Cizkova
Journal:  In Vitro Cell Dev Biol Anim       Date:  2014-04-16       Impact factor: 2.416

9.  Vascular endothelial growth factor promotes cardiac stem cell migration via the PI3K/Akt pathway.

Authors:  Junming Tang; Jianing Wang; Xia Kong; Jianye Yang; Linyun Guo; Fei Zheng; Lei Zhang; Yongzhang Huang; Yu Wan
Journal:  Exp Cell Res       Date:  2009-10-02       Impact factor: 3.905

10.  Role of whole bone marrow, whole bone marrow cultured cells, and mesenchymal stem cells in chronic wound healing.

Authors:  Luis Rodriguez-Menocal; Shahjahan Shareef; Marcela Salgado; Arsalan Shabbir; Evangelos Van Badiavas
Journal:  Stem Cell Res Ther       Date:  2015-03-13       Impact factor: 6.832

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