Efficient cell specific differentiation systems for iPSC

Sponsored by: Life Technologies
Session ends: Closed
Answers by: Dr. Mohan C Vemuri, Director of Research and Development for Cell Biology at Thermo Fisher Scientific

Introduction


The promise of human pluripotent stem cells will be realized only when these cells are successfully coaxed into different cell types found in the human body, through the process of directed differentiation. This is critical to getting the desired cell types and numbers needed for drug screening, translational cell therapy and regenerative medicine applications. Most of the existing methods of differentiation are suboptimal, involving laborious mechanical and manual steps leading to issues of reproducibility and reduced efficiency in downstream processing of functionally mature lineages. The complex developmental process of differentiation and the challenges associated need to be efficiently deciphered in order to successfully direct the hPSC differentiation to target cell types.

During this Ask the Experts session, we will be discussing the challenges associated with hPSC differentiation to neural and cardiac lineages, how Thermo Fisher Scientific can address how these processes can be efficiently simplified with tools and cGMP cell culture media systems for robust, efficient and scalable differentiation of these two critical cell lineages. Use of these reagent systems will enable researchers to precisely control and direct the differentiation to terminal lineages in a relatively easy manner, and speedily with high efficiency.

This Ask the Expert session will be hosted by Dr. Mohan C Vemuri, the Director of Research and Development for Cell Biology at Thermo Fisher Scientific. In this capacity, Dr. Vemuri leads R&D activities in stem cell product development in the areas of human iPSC, adult stem cells, immune cells and cell lineage specific differentiation in GMP environment for research use and subsequently for use in cell therapy with regulatory compliance.

Ask the Expert Image

This session is sponsored by
Life Technologies


Questions & Answers

Rapid protocol for differentiation of iPSCs into dopaminergic neurons?

Rapid in this case may not be as important as efficient. The developmental biology of TH+ neurons is not understood well enough to ‘speed up’ the development of different types of neurons including dopaminergic or cortical motor neurons. A recent study found that Dibutyryl cyclic-AMP (dbcAMP) was shown to induce up to 85% in vitro […]» Read More

What are your thoughts on single-cell sequencing vs. population averaging methods in confirming/evaluating differentiation?

Each method has its own advantages and some disadvantages. Biological phenotype is a result of a complex cellular architecture and multiple interactions of several cell types (sometimes single cells) based on their environmental niche with in the human body. Recently, advances in single cell genomic profiling approaches has created an opportunity to see and understand […]» Read More

Hi! What is the best differention medium for hepatogenic differentiation of iPS cells derived from human skin fibroblasts? Thanks.

Several researchers are working on iPSC to hepatic differentiation. Commonly, the first step required is definitive endoderm differentiation. Following the definitive endoderm fate, the cells need to be taken through posterior foregut fate and then towards hepatic. There is no one culture media to accomplish these different steps available today. Currently this process involves the […]» Read More

What would be an efficient protocol for hESCs differentiation into epidermal cells, with an optimal subculture afterwards?

Epidermal cells consist of a variety of cells including any of the cells making up the skin such as keratinocytes, melanocytes, melanoblast (precursor of melanocyte) Langerhans cells, and Merkel cells. It is important to identify the desired cell type for differentiation. Most methods for keratinocytes and melanocytes are still developing in the literature. That said, […]» Read More

I am trying to culture human iPSCs without a feeder layer and keep them undifferentiated. I am using a commercial iPSCs media. I am trying to do this without matrigel, but the cells keep differentiating. Do I need to add Matrigel or is there a way to do this without?

(A) iPSC feeder free cultures would primarily require a matrix ( substrate) and robust culture media systems to enable and sustain stem cell state and at the same time allow expansion of the iPSC within the culture system. Without a substrate and culture media system, the cells will crash. You could consider using alternative substrates […]» Read More

Our lab is differentiating iPSCs into cardiomyocytes and we have initial success for a few times then our efficiency drops. The only thing that is changing is cell density. Do you think the cell density is affecting our efficiency and if so, what kind of passaging do you recommend for the best efficiency?

iPSC quality of the starter population and seeding densities are critical for cardiac differentiation depending on the protocol you are adopting for your differentiation to cardiomyocytes. If you have expanding populations in the beginning during differentiation, the stochastic ratios alter and could lead to less robust methods of generating desired cell types. Similarly if the […]» Read More

I am looking for a system that can detect differentiation using imaging techniques that are not invasive to the culture. Do you have any recommendations?

There are two possible approaches you could use for a system to detect differentiation using non-invasive imaging techniques. The first is simple phase contrast microscopy. Using this approach you would look for the spike appearance of differentiating cells. Using imaging tools you can mask the undifferentiated cells and mark the differentiated cells. You may want […]» Read More