Features | Partner Sites | Information | LinkXpress
Sign In
Demo Company

Deletion of the FOXO1 Gene Transforms Intestinal Cells into Insulin Producers

By BiotechDaily International staff writers
Posted on 13 Jul 2014
Image: Human gastrointestinal cells from patients were engineered to express insulin (fluorescent green) in the laboratory (Photo courtesy of Columbia University).
Image: Human gastrointestinal cells from patients were engineered to express insulin (fluorescent green) in the laboratory (Photo courtesy of Columbia University).
After having demonstrated that gut endocrine progenitor cells of mice could be differentiated into glucose-responsive, insulin-producing cells by elimination of the transcription factor FOXO1 (forkhead box O1), diabetes researchers have extended these findings by obtaining similar results with human gut endocrine progenitor and serotonin-producing cells.

Generation of alternative sources of insulin-producing beta-cells has been a goal of researchers in the field of diabetes therapy. While most efforts have been directed at differentiating embryonic or induced pluripotent stem (iPS) cells into beta-like-cells, investigators at Columbia University (New York, NY, USA) have shown that shown that mouse intestinal cells could be transformed into insulin-producing cells by deactivating the cells’ FOXO1 gene.

In a paper published in the June 30, 2014, online edition of the journal Nature Communications, the investigators revealed that FOXO1 was present in human gut endocrine progenitor and serotonin-producing cells. Using gut organoids derived from human iPS cells, they demonstrated that inhibition of FOXO1 using a dominant-negative mutant or Lentivirus-encoded small hairpin RNA promoted generation of insulin-positive cells that expressed all markers of mature pancreatic beta-cells and survived in vivo following transplantation into mice.

“People have been talking about turning one cell into another for a long time, but until now we had not gotten to the point of creating a fully functional insulin-producing cell by the manipulation of a single target,” said senior author Dr. Domenico Accili, professor of diabetes at Columbia University. “By showing that human cells can respond in the same way as mouse cells, we have cleared a main hurdle and can now move forward to try to make this treatment a reality.”

Related Links:

Columbia University


Drug Discovery

view channel
Image: Endoscopic image of a bowel section known as the sigmoid colon afflicted with ulcerative colitis. The internal surface of the colon is blotchy and broken in places (Photo courtesy of Wikimedia Commons).

Orally Delivered Curcumin-Loaded Microparticles Effectively Treat Mouse Model of Ulcerative Colitis

Microparticles (MPs) loaded with the efficient anti-inflammatory agent curcumin were found to effectively treat a mouse model of ulcerative colitis. Ulcerative colitis is a chronic relapsing disease... Read more


view channel

Biopharmaceutical Partners Seek Alternatives to Glucocorticoid Steroid Drugs

Collaboration between American and Japanese biopharmaceutical companies is expected to lead to the development of a new class of small molecule drugs for treatment of hematological and inflammatory diseases. Gencia LLC (Charlottesville, VA, USA) and Takeda Pharmaceutical Company Ltd. (Osaka, Japan) announced the formation... Read more


17 Oct 2015 - 21 Oct 2015
25 Oct 2015 - 29 Oct 2015
16 Nov 2015 - 19 Nov 2015
Copyright © 2000-2015 Globetech Media. All rights reserved.