Stem cell potency

Lead Research Organisation: University of Cambridge
Department Name: Biochemistry

Abstract

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Technical Summary

Recent reports suggest that under certain conditions adult mammalian stem cells may be able to escape lineage restriction and exhibit broad differentiation capacity. If these findings can be reproduced, understood and controlled, the implications for future healthcare strategies are considerable. However, this is a very new area of research that challenges previous orthodoxies and raises basic questions about mechanisms of cell determination and genomic programming. In this proposal we aim to determine the true incidence and nature of stem cell plasticity, to achieve a molecular definition of the stem cell state, and to examine whether the developmental potency of stem cells translates into a propensity for reprogramming by nuclear transfer.
 
Description Signals and genes that control stem cells
Exploitation Route Basic and biomedical research
Sectors Healthcare,Pharmaceuticals and Medical Biotechnology

 
Description BBSRC Stem Cell Potency
Amount £841,267 (GBP)
Organisation Biotechnology and Biological Sciences Research Council (BBSRC) 
Sector Public
Country United Kingdom
Start 08/2006 
End 02/2008
 
Title CULTURE MEDIUM CONTAINING KINASE INHIBITORS. AND USES THEREOF 
Description Pluripotent cells are maintained in a self-renewing state in serum-free culture medium comprising a MEK inhibitor, a GSK3 inhibitor and, optionally, an antagonist of an FGF receptor. Pluripotent cells are also maintained in a self-renewing state in serum-free culture medium comprising a MEK inhibitor and an antagonist of an FGF receptor. 
IP Reference WO2007113505 
Protection Patent granted
Year Protection Granted 2007
Licensed No
Impact N/A
 
Title DIRECTED NEURAL DIFFERENTIATION 
Description Differentiation towards a neural fate, and away from a non-neural fate, is promoted by activation of Notch signalling in ES cells and then transferring the cells into neural differentiation protocols. Media for neural differentiation comprises a Notch activator, e.g. a notch ligand that can be clustered. Genetic manipulation is used as an alternative to media additives for Notch activation. 
IP Reference WO2006095175 
Protection Patent granted
Year Protection Granted 2006
Licensed No
Impact N/A
 
Title IMPROVED REPROGRAMMING OF MAMMALIAN CELLS, AND THE CELLS OBTAINED 
Description Expression of reprogramming factors such as Sox2, klf4, c-myc, Nanog, LIN28 and Oct4 followed by culture in a MEK inhibitor and a GSK3 inhibitor reprograms tissue cells. The invention provides new uses of these inhibitors, for example in inducing completion of the transcriptional resetting of so-called pre-pluripotent (pre-iPS) stem cells, for example as obtained from mammalian neural stem cells or epiblast stem cells treated with single or combinations of the reprogramming factors, expressed transiently or by integrative vectors. Also provided are systems for reprogramming an epiplast stem cells independently of the use of there inhibitors. 
IP Reference WO2009101407 
Protection Patent granted
Year Protection Granted 2009
Licensed Yes
Impact N/A
 
Title PLURIPOTENCY DETERMINING FACTORS AND USES THEREOF 
Description Pluripotency determining factors are described which act intracellularly and maintain a pluripotent cell in a pluripotent state in the absence of gp130 activation, which maintain or confer pluripotency of a human stem cell, which maintain or confer pluripotency of a mouse ES cell, and which maintain or confer pluripotency of a stem cell from a non-permissive strain of mice. The factors and vectors encoding or activating the factors are used to maintain and derive pluripotent cells, especially of higher mammals, including humans. 
IP Reference WO03064463 
Protection Patent granted
Year Protection Granted 2003
Licensed No
Impact n.a
 
Title REPROGRAMMING AND GENETIC MODIFICATION OF CELLS 
Description Methods for reprogramming and optional genetic modification of cells are provided. A pluripotent genome is obtained from a differentiated genome by fusing a pluripotent cell with a differentiated cell in the presence of Nanog or a MEK inhibitor. A cell is genetically modified by providing first and second cells, each containing chromosomes, fusing the first cell and the second cell, and culturing the fused cell so as to obtain a diploid cell containing at least one chromosome from the first cell and at least one chromosome form the second cell. A method of cell fusion comprises fusing a first cell and a second cell in the presence of Nanog or a MEK inhibitor. Cells obtained thereby and their uses are also described. 
IP Reference WO2007054720 
Protection Patent granted
Year Protection Granted 2007
Licensed No
Impact N/A
 
Description 25 Years of Embryonic Stem Cells in Cambridge 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? Yes
Geographic Reach National
Primary Audience Other academic audiences (collaborators, peers etc.)
Results and Impact Discussion post event
Year(s) Of Engagement Activity 2006
 
Description International Summer School, Cambridge 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Schools
Results and Impact University of Cambridge International Summer School, Guest Lecturer

N/A
Year(s) Of Engagement Activity 2006
 
Description International Summer School, Cambridge 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Schools
Results and Impact University of Cambridge International Summer School, Guest Lecturer

N/A
Year(s) Of Engagement Activity 2008
 
Description International Summer School, Cambridge 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Schools
Results and Impact University of Cambridge International Summer School, Guest Lecturer

N/A
Year(s) Of Engagement Activity 2007
 
Description Stem Cell Dream Event 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? Yes
Geographic Reach National
Primary Audience Public/other audiences
Results and Impact Platform Speaker in the Stem Cell Dream, public event

n.a
Year(s) Of Engagement Activity 2007
 
Description Stem Cell Dream Event 2008 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? Yes
Geographic Reach National
Primary Audience Public/other audiences
Results and Impact Speaker at the Stem Cell dream event - this resulted in discussion afterwards
Year(s) Of Engagement Activity 2008