TY - JOUR KW - Animals KW - Cell Movement KW - Cell Survival KW - Epigenesis, Genetic KW - Epithelial-Mesenchymal Transition KW - Granuloma KW - Host-Pathogen Interactions KW - Humans KW - leprosy KW - Macrophages KW - Mice KW - Mice, Nude KW - Mycobacterium leprae KW - Peripheral nerves KW - Schwann Cells KW - Stem Cells AU - Masaki T AU - Qu J AU - Cholewa-Waclaw J AU - Burr K AU - Raaum R AU - Rambukkana A AB -

Differentiated cells possess a remarkable genomic plasticity that can be manipulated to reverse or change developmental commitments. Here, we show that the leprosy bacterium hijacks this property to reprogram adult Schwann cells, its preferred host niche, to a stage of progenitor/stem-like cells (pSLC) of mesenchymal trait by downregulating Schwann cell lineage/differentiation-associated genes and upregulating genes mostly of mesoderm development. Reprogramming accompanies epigenetic changes and renders infected cells highly plastic, migratory, and immunomodulatory. We provide evidence that acquisition of these properties by pSLC promotes bacterial spread by two distinct mechanisms: direct differentiation to mesenchymal tissues, including skeletal and smooth muscles, and formation of granuloma-like structures and subsequent release of bacteria-laden macrophages. These findings support a model of host cell reprogramming in which a bacterial pathogen uses the plasticity of its cellular niche for promoting dissemination of infection and provide an unexpected link between cellular reprogramming and host-pathogen interaction.

BT - Cell C1 - http://www.ncbi.nlm.nih.gov/pubmed/23332746?dopt=Abstract CN - MASAKI 2013 DA - 2013 Jan 17 DO - 10.1016/j.cell.2012.12.014 IS - 1-2 J2 - Cell LA - eng N2 -

Differentiated cells possess a remarkable genomic plasticity that can be manipulated to reverse or change developmental commitments. Here, we show that the leprosy bacterium hijacks this property to reprogram adult Schwann cells, its preferred host niche, to a stage of progenitor/stem-like cells (pSLC) of mesenchymal trait by downregulating Schwann cell lineage/differentiation-associated genes and upregulating genes mostly of mesoderm development. Reprogramming accompanies epigenetic changes and renders infected cells highly plastic, migratory, and immunomodulatory. We provide evidence that acquisition of these properties by pSLC promotes bacterial spread by two distinct mechanisms: direct differentiation to mesenchymal tissues, including skeletal and smooth muscles, and formation of granuloma-like structures and subsequent release of bacteria-laden macrophages. These findings support a model of host cell reprogramming in which a bacterial pathogen uses the plasticity of its cellular niche for promoting dissemination of infection and provide an unexpected link between cellular reprogramming and host-pathogen interaction.

PY - 2013 SP - 51 EP - 67 T2 - Cell TI - Reprogramming adult Schwann cells to stem cell-like cells by leprosy bacilli promotes dissemination of infection. UR - http://onlinedigeditions.com/publication/frame.php?i=187850&p=&pn=&ver=flex VL - 152 SN - 1097-4172 ER -