Sains Malaysiana 48(3)(2019): 637–644
http://dx.doi.org/10.17576/jsm-2019-4803-17
Exploring
The Potential of Dermal Fibroblast Conditioned Medium on Skin Wound Healing and
Anti-Ageing
(Meneroka
Potensi Fibroblas Derma Medium Terkondisi untuk Penyembuhan Luka Pada Kulit dan
Anti-Penuaan)
SHIPLU ROY CHOWDHURY*, LIM SHAUN JING, MUHAMMAD NOOR HAZIQ
BIN ZOLKAFLI, NUR’ AQILAH
BINTI MOHD ABU ZARIN, WAN ALYANI
BINTI WAN ABDULLAH, NURUL AIDAH
BINTI MD MOTHAR, MANIRA MAAROF
& NUR ATIQAH HAIZUM ABDULLAH
Tissue Engineering Centre, Faculty of Medicine, Universiti
Kebangsaan Malaysia, Jalan Yaacob Latif, 56000 Cheras, Kuala Lumpur, Federal
Territory, Malaysia
Diserahkan: 17 April 2018/Diterima: 29 November 2018
ABSTRACT
Skin ageing is associated with a decrease in collagen and delayed
wound healing. The previous study has shown that supplementation of growth
factors can enhance the production of extracellular matrix (ECM)
and efficiency of wound healing. This study aimed to produce a Dermal
Fibroblast Conditioned Medium (DFCM) and evaluate its
potential on in vitro skin wound
healing and anti-ageing properties. DFCM were obtained by culturing
confluent human dermal fibroblasts (n=3) in keratinocyte-specific medium
(DFCM-KM),
fibroblast-specific medium (DFCM-FM) and
fibroblast-specific medium with growth supplements (DFCM-GM).
Protein concentration was determined by Bicinchoninic Acid (BCA)
assay. To evaluate the wound healing and anti-ageing properties, human dermal
fibroblasts were supplemented with three different DFCM.
Fibroblasts cultured with F12:DMEM+10%FBS was
used as a control. The growth rate of fibroblasts was evaluated by culturing
cells until day 4. Migration rate was evaluated at 12 h after seeding. In
vitro healing rate was evaluated via scratch assay. Anti-ageing potential of DFCM was evaluated via RT2 Profiler PCR Array.
Concentration of total protein was found to be significantly higher in DFCM-GM (2914.79±150.67mg/mL) compared to DFCM-KM and DFCM-FM.
Out of the tested 12 anti-ageing genes, fibroblasts supplemented with DFCM-GM demonstrated a significantly higher expression of WRN compared
to other conditions. In conclusion, DFCM-GM contains more proteins
and found superior in modulating wound healing and anti-ageing properties.
Keywords: Anti-ageing; conditioned medium; dermal fibroblast
conditioned medium; fibroblasts; wound healing
ABSTRAK
Penuaan kulit dikaitkan dengan pengurangan kolagen dan penyembuhan
luka yang lambat. Kajian terdahulu menunjukkan bahawa penambahan faktor
pertumbuhan boleh meningkatkan penghasilan matriks ekstrasel (ECM)
serta keberkesanan proses penyembuhan luka. Kajian ini bertujuan untuk
menghasilkan medium terkondisi daripada fibroblas (DFCM)
serta menilai kesannya terhadap proses penyembuhan luka dan anti-penuaan. DFCM diperoleh dengan mengkultur sel fibroblas derma manusia (n = 3) di dalam medium khusus keratinosit (DFCM-KM),
medium khusus fibroblas (DFCM-FM) dan medium khusus fibroblas
dengan penambahan faktor pertumbuhan (DFCM-GM). Kepekatan protein
ditentukan dengan menggunakan asai acid Bicinchoninic (BCA).
Untuk menilai proses penyembuhan luka dan anti-penuaan, kultur fibroblas
ditambah dengan tiga DFCM yang berbeza. Fibroblas yang
dikultur di dalam F12: DMEM + 10% FBS digunakan
sebagai kumpulan kawalan. Kadar pertumbuhan fibroblas dinilai melalui
pengkulturan sel sehingga hari ke-4 manakala kadar migrasi dinilai bermula dari
12 jam selepas pengkulturan. Kadar penyembuhan luka secara in vitro dinilai
menggunakan teknik pencalaran. Potensi anti-penuaan DFCM dinilai
melalui RT2 Profiler PCR Array. Kepekatan protein DFCM-GM (2914.79 ± 150.67 μg/mL) didapati jauh lebih tinggi
berbanding dengan DFCM-KM dan DFCM-FM.
Analisis pengekspresan 12 gen anti-penuaan menunjukkan bahawa ekspresi WRN pada
fibroblas yang ditambah dengan DFCM-GM adalah jauh lebih
tinggi berbanding kumpulan yang lain. Kesimpulannya, DFCM-GM mengandungi
lebih banyak protein, boleh meningkatkan serta mengawal proses penyembuhan luka
dan bersifat anti-penuaan.
Kata kunci: Anti-penuaan;
fibroblas; medium terkondisi; medium terkondisi daripada fibroblas; penyembuhan
luka
RUJUKAN
Chowdhury, S.R., Aminuddin, B.S. & Ruszymah,
B.H.I. 2012. Effect of supplementation of dermal fibroblasts conditioned medium
on expansion of keratinocytes through enhancing attachment. Indian Journal
of Experimental Biology 50: 332-339.
Eaglstein, W.H. 1986. Wound healing and aging. Dermatologic
Clinics 4(3): 481-484.
Farage, M.A., Miller, K.W., Elsner, P. &
Maibach, H.I. 2013. Characteristics of the aging skin. Advances in Wound
Care 2(1): 5-10.
Ganceviciene, R., Liakou, A.I., Theodoridis, A., Makrantonaki, E.
& Zouboulis, C.C. 2012. Skin anti-aging strategies. Dermato-endocrinology 4(3): 308-319.
Grinnell, F. &
Burgess, L. 1981. Distribution of fibronectin during wound healing in vivo. Journal of Investigative Dermatology 76(3): 181-189.
Heukeshoven, J. & Dernick, R. 1988. Improved silver
staining procedure for fast staining in PhastSystem Development Unit. I.
Staining of sodium dodecyl sulfate gels. Electrophoresis 9(1): 28-32.
Jung, S., Sen, A., Rosenberg, L. & Behie, L.A. 2012.
Human mesenchymal stem cell culture: Rapid and efficient isolation and
expansion in a defined serum-free medium. Journal of Tissue Engineering and
Regenerative Medicine 6(5): 391- 403.
Kamath-Loeb, A.S., Shen, J.C., Schmitt, M.W. & Loeb,
L.A. 2012. The Werner Syndrome exonuclease facilitates DNA degradation and
high-fidelity DNA polymerization by human DNA polymerase δ. Journal of
Biological Chemistry 287(15): 12480-12490.
Kim, W.S., Park, B.S., Sung, J.H., Yang, J.M., Park, S.B.,
Kwak, S.J. & Park, J.S. 2007. Wound healing effect of adipose-derived stem
cells: A critical role of secretory factors on human dermal fibroblasts. Journal
of Dermatological Science 48(1): 15-24.
Laemmli, U.K. 1970. Cleavage of structural proteins during
the assembly of the head of bacteriophage T4. Nature 227(5259): 680-685.
Lee, D.Y., Yang, J.M. & Park, K.H. 2007. A dermal
equivalent developed from fibroblast culture alone: Effect of EGF and insulin. Wound
Repair and Regeneration 15: 936-939.
Lee, J.W., Kusumoto, R., Doherty, K.M., Lin, G.X., Zeng, W.,
Cheng, W.H., von Kobbe, C., Brosh, R.M. Jr., Hu, J.S. & Bohr, V.A. 2005.
Modulation of Werner Syndrome protein function by a single mutation in the
conserved RecQ domain. Journal of Biological Chemistry 280(47): 39627-39636.
Manira, M., Yogeswaran, L., Ruszymah, B.H.I., Aminuddin, B.S.
& Chowdhury, S.R. 2018. Proteomic analysis of human
dermal fibroblast conditioned medium (DFCM). The Protein Journal 37: 589-607.
Manira, M., Law, J.X., Chowdhury, S.R., Khairul, A.K.,
Aminuddin, B.S. & Ruszymah, B.H.I. 2016. Secretion of wound healing
mediators by single and bi-layer skin substitutes. Cytotechnology 68(5):
1873-1884.
Manira, M., Chowdhury, S.R., Rosliza, A., Yi Ling, A.,
Abidah, A., Vittarino, J., Nurul Izzah, A., Aminuddin, B.S. & Ruszymah,
B.H.I. 2014. Concentration dependent effect of dermal fibroblast conditioned
medium on in vitro wound healing properties of keratinocytes. Regenerative
Research 3(2): 30-32.
Nurul 'Izzah, A.G., Aminuddin, B.S., Ruszymah, B.H.I. &
Chowdhury, S.R. 2016. Calcium in dermal fibroblast conditioned
medium (DFCM) enhance keratinocytes wound healing in vitro.
Abstract in 6th Malaysian Tissue Engineering & Regenerative
Medicine Scientific Meeting. p. 48.
Rando, T.A. & Chang, H.Y. 2012. Aging, rejuvenation, and
epigenetic reprogramming: Resetting the aging clock. Cell 148(1-2):
46-57.
Reed, M.J., Koike, T. & Puolakkainen, P. 2003. Wound
repair in aging. In Wound Healing. Methods in Molecular Medicine™,
edited by DiPietro, L.A. & Burns, A.L. vol 78. Totowa, NJ: Humana Press.
Richard, A.F.C. 1983. Fibronectin in the skin. The
Journal of Investigative Dermatology 81(6): 475-479.
Seet, W.T., Maarof, M., Khairul Anuar, K., Chua, K.H., Ahmad
Irfan, A.W., Ng, M.H., Aminuddin, B.S. & Ruszymah, B.H.I. 2012. Shelf-life
evaluation of bilayered human skin equivalent, MyDermTM. PLoS
ONE 7(8): e40978.
Seifert, A.W., Monaghan, J.R., Voss, S.R. & Maden, M.
2012. Skin regeneration in adult axolotls: A blueprint for scar-free healing in
vertebrates. PloS ONE 7(4): e32875.
Stephens, P. 2011. Dysfunctional wound healing in chronic
wounds. In Advanced Wound Repair Therapies, edited by David Farrar. 1st ed.
Cambridge, UK: Woodhead Publishing Limited.
Varani, J., Dame, M.K., Rittie, L., Fligiel, S.E.G., Kang,
S., Fisher, G.J. & Voorhees, J.J. 2006. Decreased collagen production in
chronologically aged skin: Roles of age-dependent alteration in fibroblast function
and defective mechanical stimulation. The American Journal of Pathology 168(6):
1861-1868.
Xie, J., Bian, H., Qi, S., Xu, Y., Tang, J., Li, T. &
Liu, X. 2008. Effects of basic fibroblast growth factor on the expression of
extracellular matrix and matrix metalloproteinase-1 in wound healing. Clinical
and Experimental Dermatology 33(2): 176-182.
*Pengarang
untuk surat-menyurat; email: shiplu@ppukm.ukm.edu.my