TY - JOUR
T1 - GABPβ2 expression during osteogenic differentiation from human osteoblast-like Saos-2 cells
AU - Xu, Xiaoyuan
AU - Xiong, Jianjun
AU - Wang, Tao
AU - Zheng, Meirong
AU - Wu, Ping
AU - Wang, Xinping
AU - Jiang, H.
AU - Yi, Benyi
AU - Lang, Bin
AU - Li, Weidong
N1 - Publisher Copyright:
© Polish Society for Histochemistry and Cytochemistry Folia Histochem Cytobiol. 2014.
PY - 2014
Y1 - 2014
N2 - The E26 transformation-specific (ETS) family of transcription factors plays an important role in osteogenic differentiation. Whether GA-binding protein β2 (GABPβ2), a member of the ETS family, is involved in osteogenic differentiation has not been previously reported. In the present study, directed differentiation of human osteoblast-like Saos-2 cells was induced and validated by examining alkaline phosphatase (ALP) activity, presence of mineralized nodule and other phenotypic characteristics of the cells on days 0, 3, 6 and 9, thus establishing their osteogenic potential. Real-time PCR revealed that similarly to the bone-specific transcription factor Runx2, the expression of Gabpb2 in Saos-2 cells also peaked on day 3 and was significantly reduced on days 6 and 9. Immunocytochemical staining showed that changes in the immunoreactivity of GABPβ2 also exhibited a similar trend to that of Runx2. Initially, Runx2 was predominantly localized in the nuclei, while GABPβ2 was relatively diffuse. Both exhibited a significant increase in immunoreactivity on day 3, with presence in both the nuclei and cytoplasm. By day 6, both showed a significant decrease in immunoreactivity and were mainly localized in the nuclei. Therefore, we surmise that GABPβ2, as an ETS family member, may play a regulatory role in early osteoblastic differentiation and potentially act in synergy with Runx2.
AB - The E26 transformation-specific (ETS) family of transcription factors plays an important role in osteogenic differentiation. Whether GA-binding protein β2 (GABPβ2), a member of the ETS family, is involved in osteogenic differentiation has not been previously reported. In the present study, directed differentiation of human osteoblast-like Saos-2 cells was induced and validated by examining alkaline phosphatase (ALP) activity, presence of mineralized nodule and other phenotypic characteristics of the cells on days 0, 3, 6 and 9, thus establishing their osteogenic potential. Real-time PCR revealed that similarly to the bone-specific transcription factor Runx2, the expression of Gabpb2 in Saos-2 cells also peaked on day 3 and was significantly reduced on days 6 and 9. Immunocytochemical staining showed that changes in the immunoreactivity of GABPβ2 also exhibited a similar trend to that of Runx2. Initially, Runx2 was predominantly localized in the nuclei, while GABPβ2 was relatively diffuse. Both exhibited a significant increase in immunoreactivity on day 3, with presence in both the nuclei and cytoplasm. By day 6, both showed a significant decrease in immunoreactivity and were mainly localized in the nuclei. Therefore, we surmise that GABPβ2, as an ETS family member, may play a regulatory role in early osteoblastic differentiation and potentially act in synergy with Runx2.
KW - GABPβ2
KW - Human osteoblast-like Saos-2 cells
KW - IHC
KW - Osteogenic differentiation
KW - QPCR
KW - Runx2
UR - http://www.scopus.com/inward/record.url?scp=84907805853&partnerID=8YFLogxK
U2 - 10.5603/FHC.2014.0026
DO - 10.5603/FHC.2014.0026
M3 - Article
C2 - 25308738
AN - SCOPUS:84907805853
SN - 0239-8508
VL - 52
SP - 225
EP - 231
JO - Folia Histochemica et Cytobiologica
JF - Folia Histochemica et Cytobiologica
IS - 3
ER -