Sains Malaysiana 48(9)(2019): 1855–1865
http://dx.doi.org/10.17576/jsm-2019-4809-06
Pengkulturan dan
Pencirian Penanda Molekul Sel Stem Manusia daripada Pulpa Gigi Susu (SHED) dan Gigi Kekal (DPSC)
(Culture and Molecular
Markers Characterization of Stem Cells from Human Deciduous (SHED)
and Permanent (DPSC) Teeth Pulp)
SHAHRUL HISHAM ZAINAL ARIFFIN1*, THANALETCHUMI MANOGARAN1, INTAN ZARINA ZAINOL ABIDIN2, ZAIDAH ZAINAL ARIFFIN3 & ROHAYA MEGAT ABDUL WAHAB4
1Pusat
Bioteknologi dan Makanan Berfungsi, Fakulti Sains dan Teknologi, Universiti
Kebangsaan Malaysia, 43600 Bangi, Selangor Darul Ehsan, Malaysia
2Centre
for Research and Postgraduate Studies, Cyberjaya University College of Medical
Sciences, 63000 Cyberjaya, Selangor Darul Ehsan, Malaysia
3Pusat
Pengajian Biologi, Fakulti Sains Gunaan, Universiti Teknologi MARA, 40450 UiTM
Shah Alam, Selangor Darul Ehsan, Malaysia
4Unit
Ortodontik, Pusat Kesihatan Pergigian Keluarga, Fakulti Pergigian, Universiti
Kebangsaan Malaysia, 50300 Kuala Lumpur, Wilayah Persekutuan, Malaysia
Diserahkan: 25
Februari 2019/Diterima: 25 Jun 2019
ABSTRAK
Sel stem pulpa gigi manusia
yang dipencilkan daripada tisu pulpa gigi merupakan sel stem dewasa
bersifat multipoten. Objektif kajian ini adalah untuk mengenal pasti
teknik pengkulturan in vitro sel stem pulpa gigi susu (SHED)
dan gigi kekal (DPSC) melalui penentuan pasaj, kesan
eraman tripsin-EDTA dan potensi proliferasi serta untuk
mencirikan kedua-dua sel ini melalui profil penanda molekul.
Kaedah pencernaan enzim digunakan pada tisu pulpa gigi susu dan
gigi kekal masing-masing untuk pemencilan sel SHED dan DPSC.
Kedua-dua sel dikulturkan daripada pasaj 1 hingga 5 dan pewarnaan
tripan biru digunakan untuk memperoleh lengkuk pertumbuhan bagi
menentukan masa penggandaan populasi sel (PDT) pada setiap pasaj. Kesan tripsin-EDTA terhadap
kedua-dua sel dikaji menggunakan pewarnaan Alamar biru untuk menentukan
masa eraman yang optimum semasa proses pengsubkulturan. Potensi
proliferasi in vitro bagi kedua-dua sel selama 21 hari ditentukan
melalui asai 3-(4,5-dimetiltiazol-2-il)-2,5-difeniltetrazolium bromida
(MTT).
Pencirian kedua-dua sel melalui pengekspresan penanda biologi molekul
ditentukan melalui pendekatan RT-PCR. Morfologi kedua-dua sel
didapati menyerupai sel fibroblas pada kesemua pasaj. Sel SHED dan
DPSC
pada pasaj 3 menunjukkan PDT terendah iaitu masing-masing
43 ± 2.3 dan 63 ± 3.1 jam. Pendedahan SHED terhadap
tripsin-EDTA menunjukkan penurunan peratus sel viabel berbanding
DPSC.
Pertumbuhan sel SHED didapati ~2.3 kali ganda lebih tinggi
berbanding DPSC. Pencirian molekul kedua-dua sel
menunjukkan pengekspresan penanda sel stem mesekima dan bukannya
penanda sel stem hematopoietik. Kesimpulannya, morfologi sel yang
homogenus dan nilai PDT
terendah yang ditunjukkan oleh sel daripada pasaj
3 menjadikannya pasaj terbaik untuk menentukan potensi proliferasi
sel dan pengekpresan penanda molekul. SHED
didapati mampu berproliferasi dengan lebih baik berbanding
DPSC.
Walau bagaimanapun, DPSC lebih rentan terhadap tripsin-EDTA
berbanding SHED. Pencirian molekul pula mendapati
kedua-dua sel merupakan sel stem jenis mesenkima.
Kata kunci: Kesan
tripsin-EDTA; masa penggandaan sel; potensi
proliferasi; profil penanda biologi molekul; sel stem pulpa gigi manusia
ABSTRACT
Human dental pulp stem
cells are adult multipotent stem cells isolated from dental pulp
tissue. Our objective was to determine in vitro culture technique
for stem cells from deciduous tooth (SHED) and permanent tooth (DPSC)
through cell passage identification, the effect of trypsin-EDTA and
proliferation potential, and to characterize both cells using molecular
markers profile. Enzyme digestion method was used on dental pulp
tissue from deciduous and permanent tooth for SHED and DPSC isolation,
respectively. Both cells were cultured at passage 1 until 5 and
trypan blue assay was used to obtain growth curve in determining
cell population doubling time (PDT)
for each passage. Effect of trypsin-EDTA on both cells were studied
using Alamar blue assay to determine optimum incubation time for
subculturing process. Cell proliferation potential for both cells
within 21 days was determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium
bromide (MTT)
assay. Cell characterization through molecular biology markers was
performed using RT-PCR. Both cells at all passages appeared fibroblast-like.
SHED and DPSC at
passage 3 exhibited the lowest PDT with 43 ± 2.3 and 63
± 3.1 h, respectively. SHED exposed to trypsin-EDTA
showed decrease in cell viability percentage compared
to DPSC.
Cell growth for SHED was ~2.3-fold higher than DPSC.
Both cells expressed mesenchymal stem cell markers and not hematopoietic
stem cell markers. In conclusion, homogenous morphology and lowest
PDT value
indicated that cells at passage 3 are the best to determine proliferation
potential and molecular markers expression. SHED proliferated
better than DPSC. However, DPSC was more resistant to trypsin-EDTA than SHED. Based on molecular marker
profile, both cells are mesenchymal stem cells.
Keywords: Cell
doubling time; human dental pulp stem cells; molecular biology markers profile;
proliferation potential; trypsin-EDTA effect
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*Pengarang untuk surat-menyurat; email:
hisham@ukm.edu.my
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