CREB3L2 Regulates Hemidesmosome Formation during Epithelial Sealing

半桥粒 细胞生物学 PI3K/AKT/mTOR通路 下调和上调 间充质干细胞 化学 转录因子 基因敲除 蛋白激酶B 生物 信号转导 基因 生物化学 基底膜
作者
Yinghui Li,Jian Zhang,Wenju Cai,Chao Wang,Zhiyong Yu,Zhiwei Jiang,Kairan Lai,Yong Wang,Guoli Yang
出处
期刊:Journal of Dental Research [SAGE]
卷期号:102 (11): 1199-1209 被引量:3
标识
DOI:10.1177/00220345231176520
摘要

The long-term success rate of dental implants can be improved by establishing a favorable biological sealing with a high-quality epithelial attachment. The application of mesenchymal stem cells (MSCs) holds promise for facilitating the soft tissue integration around implants, but the molecular mechanism is still unclear and the general application of MSC sheet for soft tissue integration is also relatively unexplored. We found that gingival tissue–derived MSC (GMSC) sheet treatment significantly promoted the expression of hemidesmosome (HD)–related genes and proteins in gingival epithelial cells (GECs). The formation of HDs played a key role in strengthening peri-implant epithelium (PIE) sealing. Further, high-throughput transcriptome sequencing showed that GMSC sheet significantly upregulated the PI3K/AKT pathway, confirming that cell adhesion and HD expression in GECs were regulated by GMSC sheet. We observed that the expression of transcription factor CREB3L2 in GECs was downregulated. After treatment with PI3K pathway inhibitor LY294002, CREB3L2 messenger RNA and protein expression levels were upregulated. Further experiments showed that overexpression or knockdown of CREB3L2 could significantly inhibit or promote HD-related genes and proteins, respectively. We confirmed that CREB3L2 was a transcription factor downstream of the PI3K/AKT pathway and participated in the formation of HDs regulated by GMSC sheet. Finally, through the establishment of early implant placement model in rats, we clarified the molecular function of CREB3L2 in PIE sealing as a mechanical transmission molecule in GECs. The application of GMSC sheet–implant complex could enhance the formation of HDs at the implant–PIE interface and decrease the penetration distance of horseradish peroxidase between the implant and PIE. Meanwhile, GMSC sheet reduced the length of CREB3L2 protein expression on PIE. These findings elucidate the potential function and molecular mechanism of MSC sheet regulating the epithelial sealing around implants, providing new insights and ideas for the application of stem cell therapy in regenerative medicine.
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