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PLAC1 is involved in human trophoblast syncytialization.
Chang, Wen-Lin; Wang, Huiying; Cui, Lina; Peng, Nan-Ni; Fan, Xiujun; Xue, Li-Qun; Yang, Qing.
Afiliação
  • Chang WL; College of Veterinary Medicine, Hunan Agricultural University, Changsha, China; State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China; Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Institute of Urology, Pek
  • Wang H; Beijing Shijitan Hospital, Capital Medical University, Beijing, China; Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
  • Cui L; State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China; Graduate School of Chinese Academy of Sciences, Beijing, China.
  • Peng NN; Reproductive Medical Center of Luohu Hospital Shenzhen, Shenzhen, Guangdong, China.
  • Fan X; Laboratory for Reproductive Health, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Xue LQ; College of Veterinary Medicine, Hunan Agricultural University, Changsha, China. Electronic address: liqun_xue@aliyun.com.
  • Yang Q; College of Veterinary Medicine, Hunan Agricultural University, Changsha, China. Electronic address: qingyanghn@hunau.edu.cn.
Reprod Biol ; 16(3): 218-224, 2016 Sep.
Article em En | MEDLINE | ID: mdl-27692364
ABSTRACT
Placenta specific protein 1 (PLAC1) is thought to be important for murine and human placentation because of its abundant expression in placenta; however, the trophoblast subtypes that express PLAC1 at the fetomaternal interface and the major role of PLAC1 in placentation are still unclear. This study investigated the expression pattern of PLAC1 at the human fetomaternal interface and its involvement in trophoblast syncytialization. Localization of PLAC1 at the fetomaternal interface was studied using in situ hybridization (ISH) and immunohistochemistry (IHC) assays. Real time RT-PCR and Western Blot were employed to exhibit the expression pattern of PLAC1 during human spontaneous syncytialization of term primary cytotrophoblast cells (CTBs). Spontaneous syncytialization of a primary term CTBs model transfected with siRNA specific to PLAC1 was used to investigate the role of PLAC1 during human trophoblast syncytialization. The results showed that PLAC1 was mainly expressed in the human villous syncytiotrophoblast (STB) layer throughout gestation, and the expression level of PLAC1 was significantly elevated during human trophoblast syncytialization. Down-regulation of PLAC1 via specific PLAC1 siRNA transfection attenuated spontaneous syncytialization of primary term CTBs (p<0.05) as indicated by cell fusion index and the expression patterns of the corresponding markers. These data demonstrate the facilitative role of PLAC1 in normal human trophoblast syncytialization.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Placentação / Proteínas da Gravidez / Trofoblastos / Regulação da Expressão Gênica no Desenvolvimento Limite: Female / Humans / Pregnancy Idioma: En Revista: Reprod Biol Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Placentação / Proteínas da Gravidez / Trofoblastos / Regulação da Expressão Gênica no Desenvolvimento Limite: Female / Humans / Pregnancy Idioma: En Revista: Reprod Biol Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2016 Tipo de documento: Article