TY - JOUR
T1 - Inhibitory effect of retinoic acid receptor agonists on in vitro chondrogenic differentiation
AU - Sumitani, Yusuke
AU - Uchibe, Kenta
AU - Yoshida, Kaya
AU - Weng, Yao
AU - Guo, Jiajie
AU - Yuan, Haoze
AU - Ikegame, Mika
AU - Kamioka, Hiroshi
AU - Okamura, Hirohiko
N1 - Funding Information:
This study was supported in part by JSPS KAKENHI [Grant Numbers JP16K21186 (to K.U.) and JP19H03859 (to H.K.)].
Publisher Copyright:
© 2019, Japanese Association of Anatomists.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Retinoic acid (RA), an active metabolite of vitamin A, plays pivotal roles in a wide variety of biological processes, such as body patterning, organ development, and cell differentiation and proliferation. RA signaling is mediated by nuclear retinoic acid receptors, α, β, and γ (RARα, RARβ, and RARγ). RA is a well-known regulator of cartilage and skeleton formation and RARs are also essential for skeletal growth and hypertrophic chondrocyte-specific gene expression. These important roles of RA and RARs in chondrogenesis have been widely investigated using in vivo mouse models. However, few reports are available on the function of each subtype of RARs on in vitro chondrocyte differentiation. Here, we examined the effect of specific agonists of RARs on chondrogenic differentiation of ATDC5 and C3H10T1/2 cells. Subtype-specific RAR agonists as well as RA decreased the expressions of chondrogenic differentiation marker genes and inhibited chondrogenic differentiation, which was accompanied with morphological change to spindle-shaped cells. Among RAR agonists, RARα and RARγ agonists revealed a strong inhibitory effect on chondrogenic differentiation. RARα and RARγ agonists also hampered viability of ATDC5 cells. These observations suggested that RARα and RARγ are dominant receptors of RA signaling that negatively regulate chondrogenic differentiation.
AB - Retinoic acid (RA), an active metabolite of vitamin A, plays pivotal roles in a wide variety of biological processes, such as body patterning, organ development, and cell differentiation and proliferation. RA signaling is mediated by nuclear retinoic acid receptors, α, β, and γ (RARα, RARβ, and RARγ). RA is a well-known regulator of cartilage and skeleton formation and RARs are also essential for skeletal growth and hypertrophic chondrocyte-specific gene expression. These important roles of RA and RARs in chondrogenesis have been widely investigated using in vivo mouse models. However, few reports are available on the function of each subtype of RARs on in vitro chondrocyte differentiation. Here, we examined the effect of specific agonists of RARs on chondrogenic differentiation of ATDC5 and C3H10T1/2 cells. Subtype-specific RAR agonists as well as RA decreased the expressions of chondrogenic differentiation marker genes and inhibited chondrogenic differentiation, which was accompanied with morphological change to spindle-shaped cells. Among RAR agonists, RARα and RARγ agonists revealed a strong inhibitory effect on chondrogenic differentiation. RARα and RARγ agonists also hampered viability of ATDC5 cells. These observations suggested that RARα and RARγ are dominant receptors of RA signaling that negatively regulate chondrogenic differentiation.
KW - Chondrocyte
KW - Chondrogenesis
KW - Differentiation
KW - Retinoic acid
KW - Retinoic acid receptor
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U2 - 10.1007/s12565-019-00512-3
DO - 10.1007/s12565-019-00512-3
M3 - Article
C2 - 31732869
AN - SCOPUS:85075155051
SN - 1447-6959
VL - 95
SP - 202
EP - 208
JO - Anatomical Science International
JF - Anatomical Science International
IS - 2
ER -