HABP4 overexpression promotes apoptosis in goat turbinate bone cells

• Published in: Animal biotechnology Vol. 34; no. 9; pp. 4187 - 4195
• Main Authors: Wang, Xianjun, Hua, Xiang, Zhang, Huanrong, Ren, Yupeng, Yang, Falong, Zhu, Jiangjiang
• Format: Journal Article
• Language: English
• Published: Abingdon Taylor & Francis 11.12.2023; Taylor & Francis Ltd
• Subjects: Apoptosis; Bcl-2 protein; Bone; cell apoptosis; Cell cycle; Cell growth; Cell proliferation; Gene expression; goat; HABP4; Hyaluronic acid; interference; overexpression; p53 Protein; Poly(ADP-ribose) polymerase
• ISSN: 1049-5398; 1532-2378
• DOI: 10.1080/10495398.2022.2062601

Hyaluronic acid-binding protein (HABP4) plays important roles in regulating cell cycle and apoptosis. However, its functions in regulating cell apoptosis remain unclear. To reveal the effects of HABP4 on cell proliferation, cell cycle and apoptosis, the HABP4 sequence was cloned, and we investigated the gain and loss functions of HABP4 in goat turbinate bone cells. Our results showed that a 1,496-bp HABP4 sequence was cloned successfully. The interference effect of siRNA1 on HABP4 was the strongest, reducing its mRNA expression level by 83%, decreasing the cells in the G0/G1 and S phases of the cell cycle and inhibiting cell growth and apoptosis. The overexpression of HABP4 produced contrasting results. Furthermore, an HABP4 knockdown caused the up-regulated expression of genes associated with apoptosis, including Bcl-2 and BCL2L11, but the down-regulation of Caspase3, Caspase7, Bax, PARP1, SOCS2 and P53 mRNA levels. Additionally, HABP4 overexpression significantly up-regulated the expression levels of Bax, Caspase3, Caspase7, BCL2L11, P53, SOCS2 and PARP1. However, the expression of Bcl-2 was down-regulated. These data provide an important foundation for further in-depth studies of HABP4 functions.