iPS- #1 Breakthrough of 2008 Now at Allele!

Hailed as Science Magazine’s “#1 Breakthrough of the Year” for 2008, induced pluripotent stem (iPS) cell research is proving to be the most promising means of worldwide disease comprehension and eradication since the discovery of penicillin. iPS research is moving fast and institutions are racing to make the coveted advancements to: reveal the triggering and oppressing mechanisms of the four pluripotency inducing genes, elucidate how a cell is assigned a role by investigating cell protein signaling pathways, and reduce possible side effects like cancerous tumors at iPS cell therapy sites. As an in vitro reagent, iPS cells, unlike human cell lines, can be easily maintained in the lab. By maintaining iPS cell lines from patients with diseases like Parkinson’s it is possible for researchers to examine disease pathology in an affected living cell in ways that cannot be done with in vivo cells. Thanks to induced pluripotency, these cell lines can be created with simple, non-invasive hair follicle procurements! Additionally, juxtaposed to the 10 years of controversy following the discovery of human embryonic stem cells, induced pluripotent stem cells will not elicit the same moral or bioethical dilemmas followed by political interference due to their fully developed origin.

Author of Breakthrough of the Year: Reprogramming Cells, Gretchen Vogel stated, “…several more breakthroughs are needed before cellular reprogramming yields its first cure for disease.” Researchers must take advantage of Allele Biotech’s ground-breaking iPS product line. Our scientists have done all the preliminary work to design and construct these easy to use iPS kits to make this phenomenal field of study accessible to all. The global challenge for iPS discovery has begun!

Tags: Allele Biotech, induced pluripotent stem cells, iPS, ips stem cell lines, research kits, science and bioethics, Science Magazine Top Breakthroughs, scientific breakthrough 2008, stem cell controversey

Episomal Expression of iPS Inducing Genes — No Trace of Transgenes Afterwards

The potential use of induced pluripotent stem cells (iPS) in basic research and therapeutics is still mostly on the level of imagination. However, few doubt that this field will be one of the most actively contested and fastest evolving research topics in recent history. It reminds me of the early days of RNAi discovery, when 5 papers on DNA-based shRNA/RNAi appeared within a span of a few days (one draft from the Allele team was considered a few days too late to catch up with Nature Biotech by Science, but in the end we were the only recipient of patents on the subject).

The latest big news is a publication in Science by Junying Yu et al in the Thomson lab, who induced human iPS by using OriP/EBNA1 plasmid vector [1]. This method avoids integration of transgenes into the genome, thus reducing the risk of causing mutations.

A bit about the background: OriP/EBNA1 system originated from Epstein-Bar virus, which allows the establishment of stable episomes at 5-20 copies per cell, and duplication occurs once per cell division.

There are very few suppliers of vectors with the OriP/EBNA1, because of low demand (I was told so by the only supplier at the time, which explains why it was terminated altogether). The Phoenix™ Retrovirus system (for pdf from Orbigen, now part of Allele download from here) actually has the complete episomal cassette on the packing vector pBMN, which if not used in packaging Eco or Ampho cells, will behave as a regular plasmid. Therefore, the Retrovirus based iPS product within Allele’s iPS product group will provide two systems in one: a retroviral vector as published by Takahashi et al, and a OriP/EBNA1 system by Yu et al. They will also contain the brightest green fluorescent protein, mWasabi.

1. Yu, J., et al., Human Induced Pluripotent Stem Cells Free of Vector and Transgene Sequences. Science, 2009.

Tags: adenovirus, episomal, Epstein-Barr nuclear antigen-1, exogenous reprogramming factors, free of vector, human stem cells, iPS, lentivirus, OriP/EBNA1, plasmid vectors, retrovirus, without integration

Launch of Allele-iPS Product Line

Induced pluripotent stem cells, or iPS (or iPSC as some call it), are differentiated cells from adult that “regained” capabilities to differentiate into all 3 germ layer specific cell types. The iPS induction process currently involves using viral vectors to introduce 3 or 4 cDNAs, which seemed surprisingly simple considering how complex it is for stem cells to go through each differentiation pathway.

The potentials of using iPS as models for research, cell assay systems, drug screening, toxicological testing, etc., seem to be tremendous at this point. However, for therapeutic use, the biggest hurdle standing in the way is the tendency of these iPS cells to form tumors once transplanted. It could be due to the oncogenic nature of the stemness inducing cDNAs themselves, or the retrovirus or lentivirus used for bring the cDNAs into the cells. A number of labs like that of Sheng Ding at Scripps, San Diego (Li et al., 2009), and Doug Melton at Harvard (Huangfu et al., 2008a; Huangfu et al., 2008b), are screening chemicals that would replace the use of some or maybe eventually all of the cDNAs. Such advances may help mitigate the oncogenic effects possibly associated with the inducing genes. Using non-integrating vectors as carriers would be preferred method for gene transfer if the retroviral or lentiviral vectors are the cause of tumors from iPS.

Today is the day that Allele launches its iPS product line, officially in this exciting field as one of the very first companies that produce products to make iPS research easier for everybody. New products in the pipeline include those for iPS induction and detection, stem cell culturing, differentiation tracking, and safer, novel delivery methods. It is just the beginning!

Huangfu, D., Maehr, R., Guo, W., Eijkelenboom, A., Snitow, M., Chen, A.E., and Melton, D.A. (2008a). Induction of pluripotent stem cells by defined factors is greatly improved by small-molecule compounds. Nature biotechnology 26, 795-797.
Huangfu, D., Osafune, K., Maehr, R., Guo, W., Eijkelenboom, A., Chen, S., Muhlestein, W., and Melton, D.A. (2008b). Induction of pluripotent stem cells from primary human fibroblasts with only Oct4 and Sox2. Nature biotechnology 26, 1269-1275.
Li, W., Wei, W., Zhu, S., Zhu, J., Shi, Y., Lin, T., Hao, E., Hayek, A., Deng, H., and Ding, S. (2009). Generation of rat and human induced pluripotent stem cells by combining genetic reprogramming and chemical inhibitors. Cell stem cell 4, 16-19.

Tags: antibodies, cancer stem cells, CSCs, iPS, lentivirus, Nanog, Oct3, oncogenic, primer set, reprogramming, retrovirus, stem cells, tumor

NIH Challenge Grant, First Released Program Based on the Stimulus Fund

At least 200 million dollars will be channeled through a new, one off mechanism called the Challenge Grants that were designed as jumpstart funds for 2-year projects. The review process will be quicker than normal; the start date will be by the end of September 09. Among the topics are 15 areas designated as Specific Challenge Topics by the NIH, and high priority topics that individual institute such as the NCI added by their choices. For instance, the Clinical Proteomic Technologies for Cancer program, of which Allele is a participant through a cancer marker antibody development project, is running several proteomic related topics that the Challenge Grants will fund.

Many new areas such as iPS, cancer stem cells, and resource development for stem cells are among the selected topics. All domestic institutions, academic or for-profit, are encouraged to apply. This announcement came a couple of weeks after the passage of the stimulus bill, from the NIH that does not yet have a permanent director or a HHS boss, one has to commend it as efficient work with focus. We are expecting that more programs are to come every week here on out until it becomes clear how all ARRA (The American Recovery and Reinvestment Act of 2009 or the stimulus fund) will be spent in the biomedical research field.

Tags: 200 million, Allele, antibody selection, ARRA, Challenge Grants, iPS, NCI, NIH, stem cells, stimulus package

Reprogramming Life

President Obama is expected to lift the ban on federal fund for embryonic stem cell research soon. However, that does not seem to be the hottest topic these days concerning stem cell research. In 2006, Shinya Yamanaka showed that mouse skin cells could be reprogrammed back into something called induced pluripotent stem (iPS) cells by introducing a handful of cDNAs using retroviral vectors. The process was later repeated in human cells and by other groups including those of Thomson and Melton, sometimes with a slightly different set of inducing cDNAs, or with chemicals or shRNA repressing the repressors of the inducer genes.

The iPS cells are not exactly the same as ES cells, and no animals have been created using iPS cells, but they are close enough to be of great interest to lots of people, particularly for basic research purposes. The method to create iPS by reversing chromosomal changes along differentiation pathways appears to be surprisingly simple, like erasing an old audio tape, there may still be acoustic information left if analyzed by the right equipment, but to most people it is as clean as new. You’d wish a few things in life could be reversed that easily!

For labs that are not already in the stem cell field but feel a need to get their feet wet, then they want reagents that are pre-assembled and pre-tested. Such reagents may include: iPS cultures, iPS inducing viral particles, antibodies to stem cell specific markers, cell assays, and even PCR primer sets (synthesizing hundreds of oligos used in the Yamanaka papers alone will take a lot time and unnecessary costs). That’s where a fast-moving, research-oriented company like Allele comes in. We will bring what we think as starter sets for you, and listen to what you think as needed as we along. The new iPS product line will be launched within weeks, hopefully coinciding with our brand new webpages for all our current product lines!

Tags: c-myc, desease tissue regeneration, differetiation, iPS, Klf4, Lin28, Nanog, Oct3/4, pathways, pluripotent, re-programming, Sox2, stem cells, therapy