論文 - 詳細
| RRC ID | 75046 |
|---|---|
| 著者 | Zhang H, Yamaguchi T, Kawabata K. |
| タイトル | The maturation of iPS cell-derived brain microvascular endothelial cells by inducible-SOX18 expression. |
| ジャーナル | Fluids Barriers CNS |
| Abstract |
BACKGROUND:Brain microvascular endothelial cells (BMECs) play a major role in the blood-brain barrier (BBB), and are critical for establishing an in vitro BBB model. Currently, iPSC-derived BMECs (iBMECs) have been used to construct in vitro BBB models with physiological barrier functions, such as high trans-endothelial electrical resistance (TEER) and expression of transporter proteins. However, the relatively low p-glycoprotein (P-gp) level and a decrease in the efflux ratio of its substrates in iBMECs suggest their immature nature. Therefore, more mature iBMECs by optimizing the differentiation induction protocol is beneficial for establishing a more reliable in vitro BBB model for studying central nervous system (CNS) drug transport. METHODS:To identify human brain endothelial cell fate-inducing factors, HUVEC was transfected with Zic3A-, Zic3B-, and Sox18-expressing lentivirus vector. Since SOX18 was found to induce BMEC properties, we used a Dox-inducible Tet-on system to express SOX18 during iBMEC differentiation and explored the impact of SOX18 expression on iBMEC maturation. RESULTS:Sox18-mediated iBMECs achieved a higher TEER value than normal iBMECs (> 3000 Ω cm2). From day 6 to day 10 (d6-10 group), the iBMECs with SOX18 expression expressed a series of tight junction markers and showed upregulation of Mfsd2a, a specific marker of the BBB. The d6-10 group also expressed SLC2A1/Glut1 at levels as high as normal iBMECs, and upregulated ABCB1/P-gp and ABCC1/MRP1 expression. Moreover, Sox18-mediated iBMECs showed higher viability than normal iBMECs after puromycin treatment, indicating that SOX18 expression could upregulate P-gp activity in iBMECs. CONCLUSIONS:Inducible SOX18 expression in iBMECs gained BBB phenotypes, including high TEER values and upregulation of tight junction-related genes, endothelial cell (EC) markers, BBB transporters, and higher cell viability after treatment with puromycin. Collectively, we provide a differentiation method for the maturation of human iPS cell-derived BMECs with SOX18 expression, describing its contribution to form an in vitro BBB model for CNS drug transport studies. |
| 巻・号 | 20(1) |
| ページ | 10 |
| 公開日 | 2023-2-2 |
| DOI | 10.1186/s12987-023-00408-5 |
| PII | 10.1186/s12987-023-00408-5 |
| PMID | 36732767 |
| PMC | PMC9893670 |
| MeSH | Blood-Brain Barrier / metabolism Brain / blood supply Cells, Cultured Endothelial Cells* / metabolism Humans Induced Pluripotent Stem Cells* / physiology SOXF Transcription Factors / metabolism |
| IF | 4.47 |
| リソース情報 | |
| 遺伝子材料 | CSII-EF-MCS-IRES2-Venus (RDB04384) CSIV-TRE-RfA-CMV-KT (RDB12876) pCMV-VSV-G-RSV-Rev (RDB04393) pCAG-HIVgp (RDB04394) |