Silvano Serena, Napolitano Tiziana, Plaisant Magali, Sousa-De-Veiga Anette, Fofo Hugo, Ayachi Chaïma, Allegrini Benoit, Rekima Samah, Pichery Estelle, Becam Jérôme, Lepage Valentin, Treins Caroline, Etasse Laura, Tran Loan, Thévenet Julien, Pasquetti Gianni, Kerr-Conte Julie, Pattou François, Botti Paolo, Arduini Arduino, Mizrahi Jacques, Charles Benjamin, Collombat Patrick
DiogenX, 180 Avenue du Prado, 13008 Marseille, France.
University Nice Cote D'Azur, Inserm, CNRS, iBV, 06100 Nice, France; iBV, Institut de Biologie Valrose, University Nice Sophia Antipolis, Centre de Biochimie, Parc Valrose, 28, Avenue Valrose, 06108 Nice Cedex 2, France.
Cell Rep Med. 2025 May 20;6(5):102126. doi: 10.1016/j.xcrm.2025.102126. Epub 2025 May 7.
Inducing the neogenesis of pancreatic insulin-producing β cells holds great promise for diabetes research. However, non-toxic compounds with such activities remain to be discovered. Herein, we report the identification of RSPO1, a key agonist of the Wnt/β-catenin pathway, as an inducer of β cell replication. Specifically, we provide evidence that RSPO1 promotes a significant increase in β cell neogenesis in vitro, ex vivo, and in vivo. Importantly, RSPO1 administration is sufficient to activate Wnt/β-catenin signaling in β cells and counter chemically induced or autoimmune-mediated diabetes. Similarly, an optimized analog of RSPO1, allowing for weekly administration, also prevents diabetes in vivo. Lastly, the treatment of transplanted human islets with RSPO1 induces a significant 2.78-fold increase in human β cell numbers in only 60 days, these cells being functional. Such activities of RSPO1 to promote β cell neogenesis could therefore represent an unprecedented hope in the continued search for diabetes alternative therapies.
诱导胰腺胰岛素分泌β细胞的新生对糖尿病研究具有巨大的前景。然而,具有此类活性的无毒化合物仍有待发现。在此,我们报告了RSPO1(Wnt/β-连环蛋白通路的关键激动剂)作为β细胞复制诱导剂的鉴定。具体而言,我们提供证据表明RSPO1在体外、离体和体内均能显著促进β细胞新生。重要的是,给予RSPO1足以激活β细胞中的Wnt/β-连环蛋白信号,并对抗化学诱导或自身免疫介导的糖尿病。同样,一种优化的RSPO1类似物,允许每周给药一次,也能在体内预防糖尿病。最后,用RSPO1处理移植的人胰岛,仅在60天内就能使人类β细胞数量显著增加2.78倍,这些细胞具有功能。因此,RSPO1促进β细胞新生的此类活性可能代表了在持续寻找糖尿病替代疗法方面前所未有的希望。