Patricia A Murray1, Adrian S Woolf. 1. aInstitute of Translational Medicine, University of Liverpool, Liverpool bInstitute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre and the Royal Manchester Children's Hospital, Manchester, UK.
Abstract
PURPOSE OF REVIEW: There is considerable interest in the idea of generating stem and precursor cells that can differentiate into kidney cells and be used to treat kidney diseases. Within this field, we highlight recent research articles focussing on mesenchymal stem cells (MSCs), embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs) and kidney-derived stem/progenitor cells (KSPCs). RECENT FINDINGS: In preclinical studies, MSCs ameliorate varied acute and chronic kidney diseases. Their efficacy depends on immunomodulatory and paracrine properties but MSCs do not differentiate into functional kidney epithelia. iPSCs can be derived from healthy individuals and from kidney patients by forced expression of precursor genes. Like ESCs, iPSCs are pluripotent and so theoretically they have the potential to form functional kidney epithelia when used therapeutically. KSPCs, existing as cell subsets within adult and developing kidneys, constitute attractive future therapeutic agents. SUMMARY: Results from preclinical studies are encouraging but caution is required regarding potential human therapeutic applications because molecular, morphological and functional characterization of 'kidney cells' generated from ECSs, iPSCs, KSPCs have not been exhaustive. The long-term safety of renal stem and precursor cells needs more study, including potential negative effects on renal growth and their potential for tumor formation.
PURPOSE OF REVIEW: There is considerable interest in the idea of generating stem and precursor cells that can differentiate into kidney cells and be used to treat kidney diseases. Within this field, we highlight recent research articles focussing on mesenchymal stem cells (MSCs), embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs) and kidney-derived stem/progenitor cells (KSPCs). RECENT FINDINGS: In preclinical studies, MSCs ameliorate varied acute and chronic kidney diseases. Their efficacy depends on immunomodulatory and paracrine properties but MSCs do not differentiate into functional kidney epithelia. iPSCs can be derived from healthy individuals and from kidney patients by forced expression of precursor genes. Like ESCs, iPSCs are pluripotent and so theoretically they have the potential to form functional kidney epithelia when used therapeutically. KSPCs, existing as cell subsets within adult and developing kidneys, constitute attractive future therapeutic agents. SUMMARY: Results from preclinical studies are encouraging but caution is required regarding potential human therapeutic applications because molecular, morphological and functional characterization of 'kidney cells' generated from ECSs, iPSCs, KSPCs have not been exhaustive. The long-term safety of renal stem and precursor cells needs more study, including potential negative effects on renal growth and their potential for tumor formation.
Authors: Lauren Scarfe; Nathalie Brillant; J Dinesh Kumar; Noura Ali; Ahmed Alrumayh; Mohammed Amali; Stephane Barbellion; Vendula Jones; Marije Niemeijer; Sophie Potdevin; Gautier Roussignol; Anatoly Vaganov; Ivana Barbaric; Michael Barrow; Neal C Burton; John Connell; Francesco Dazzi; Josefina Edsbagge; Neil S French; Julie Holder; Claire Hutchinson; David R Jones; Tammy Kalber; Cerys Lovatt; Mark F Lythgoe; Sara Patel; P Stephen Patrick; Jacqueline Piner; Jens Reinhardt; Emanuelle Ricci; James Sidaway; Glyn N Stacey; Philip J Starkey Lewis; Gareth Sullivan; Arthur Taylor; Bettina Wilm; Harish Poptani; Patricia Murray; Chris E P Goldring; B Kevin Park Journal: NPJ Regen Med Date: 2017-10-19