Adenoviral vector-mediated expression of the pancreatic and duodenal homeobox 1 gene (Pdx1; current designation in mice insulin promotor factor-1, Ipf1) in mice has previously been reported to result in hepatic, glucose-regulated insulin secretion sufficient to ameliorate experimentally induced diabetes . In studies designed to assess the clinical applicability of this approach, we developed a protocol employing non-human primates rendered insulin-deficient (and therefore diabetic) through selective intra-arterial streptozotocin (STZ) infusion into the pancreas . We obtained and amplified the adenoviral vector in which the CMV promoter drives rat Pdx1 expression (Ad-CMV-Pdx1 referred to hereafter as Ad-Pdx1), kindly provided by S. Ferber, Endocrine Institute, Sheba Medical Centre, Tel-Hashomer, Israel.
In order to document vector activity prior to proceeding to the large animal model, we tested Ad-Pdx1 lots for activity in 8- to 10-week-old C57Bl6 mice (Jackson Laboratories, Bar Harbor, ME, USA), which were housed and handled in accordance with the guidelines set forth by the Committee on the Care and Use of Laboratory Animals of the Institute of Laboratory Animal Resources in a protocol approved by the Animal Care and Use Committee of the National Institute of Diabetes, Digestive, and Kidney Diseases. Mice were rendered diabetic with STZ (200 mg/kg i.p.). We treated 40 mice with the Ad-Pdx1 vector, but compared with control mice, observed no improvement in glycaemia. All the mice lost significant weight and subsequently had to be killed (Fig. 1a), further supporting the absence of an insulin anabolic effect.
To test whether our negative results could be explained by the vector’s failure to promote Ipf1 expression, we employed quantitative real-time PCR (qPCR) to assay for both Ipf1 and insulin, and western blotting to assess IPF1 protein expression. These assays clearly indicated vector-driven Ipf1 expression in the liver of Ad-Pdx1-treated mice; RNA was detected at a low PCR cycle number, and western blotting revealed IPF1 protein levels comparable to that from a rat insulinoma cell line (Fig. 1b,c). In order to further quantitate insulin gene expression, we removed approximately 25% of a control mouse liver, divided it into four quarters, and extracted RNA; one quarter was used as a negative control, and to the other three we added the RNA extracted from either 100, 10 or 1 mouse islets. While insulin RNA from one islet was easily detectable (Table 1), that from Ad-Pdx1-treated mouse livers was at (shown) or below the limit of detection using 40 PCR cycles, similar to the negative control liver (final amplification plot in black). These results demonstrate that the hepatic insulin message induced by Ad-Pdx1 is less than that of one islet’s RNA mixed with RNA from one-sixteenth of a liver. As four more PCR cycles were required to detect insulin message from the Ad-Pdx1-treated liver (assuming the signal represents specific amplification) compared with the cycle number when one islet was mixed with one-sixteenth of a control mouse liver, the Ad-Pdx1-induced insulin message was 24 or 16-fold less than the insulin message resulting from one islet in one-sixteenth of a liver control. Thus, the overall liver insulin RNA content induced by Ad-Pdx1 is less than that of 1 islet equivalent.
While Ipf1-induced hepatic insulin production (however minimal) is intriguing, these data are consistent with our in vivo results. That is, such negligible insulin production is unlikely to significantly improve glycaemia control. Ferber et al. also found only very low levels of hepatic insulin in their non-diabetic mice (far lower than that of the native pancreas) . Together, these data suggest that an alternative explanation must be considered for the improved glycaemia reported in that study in diabetic animals treated with Ad-Pdx1. Indeed, some of our mice were also normoglycaemic, but only when fasted (they remained hyperglycaemic in the non-fasting state). We suggest that the hepatitis associated with Ad-Pdx1 gene delivery  may have decreased mouse food intake over the brief period monitored. Certainly, before insulin treatment was available, starvation was the standard of care for diabetes, and while controlled starvation helped lower blood glucose and prolong life, the treatment was associated with inexorable wasting and death . In their initial report , Ferber et al. did not record diabetic and control mouse weights, so we cannot address the possibility that weight loss explained their observations. In addition, the earlier report did not provide details on insulin expression in the diabetic mice. Interestingly, Kojima et al. recently reported liver insulin gene expression in mice with STZ-induced diabetes , raising the possibility that the liver retains cells capable of responding to hyperglycaemia, and this may have accounted for at least some of the effect reported by Ferber et al. We conclude that liver Ipf1 gene expression is insufficient to correct experimentally induced diabetes. Our results also demonstrate the vital importance of carefully quantifying gene expression  in pre-clinical as well as clinical studies related to potential gene therapy applications.
Ferber S, Halkin A, Cohen H et al (2000) Pancreatic and duodenal homeobox gene 1 induces expression of insulin genes in liver and ameliorates streptozotocin-induced hyperglycemia. Nat Med 6:568–572
Tal MG, Hirshberg B, Neeman Z et al (2004) Induction of diabetes in nonhuman primates by means of temporary arterial embolization and selective arterial injection of streptozotocin. Radiology 230:163–168
Ber I, Shternhall K, Perl S et al (2003) Functional, persistent, and extended liver to pancreas transdifferentiation. J Biol Chem 278:31950–31957
Feudtner JC (2003) Bittersweet: diabetes, insulin, and the transformation of illness, vol 2. University of North Carolina Press, Chapel Hill
Kojima H, Fujimiya M, Matsumura K et al (2004) Extrapancreatic insulin-producing cells in multiple organs in diabetes. Proc Natl Acad Sci USA 101:2458–2463
Rajagopal J, Anderson WJ, Kume S et al (2003) Insulin staining of ES cell progeny from insulin uptake. Science 299:363
This research was supported by the Intramural Research Program of the National Institute Diabetes and Digestive and Kidney disease, National Institutes of Health.
Duality of interest statement
The authors state that they have no duality of interest.
About this article
Cite this article
Perl, S., Hirshberg, B., Harlan, D.M. et al. How much insulin is enough? A quantitative assessment of the transdifferentiaton potential of liver. Diabetologia 50, 690–692 (2007). https://doi.org/10.1007/s00125-006-0549-0
- Insulin Gene Expression
- Gene Therapy Application
- Pdx1 Expression
- Insulinoma Cell Line