Christophe Heinrich Team Leader / CR1
Until the last half of the 20th century, it was commonly believed that cell differentiation was unidirectional and irreversible. Strikingly, Gurdon and Yamanaka then made groundbreaking discoveries demonstrating instead that the identity of differentiated cells is not irreversibly determined but can be reprogrammed to a pluripotent state under appropriate signals. Importantly, seminal studies also showed that it is possible to turn one differentiated cell type directly into another without transitioning through a pluripotent ground state. This process has been termed direct lineage reprogramming.
Direct reprogramming or cell-fate conversion across cell lineages emerges as an innovative approach toward cell-based therapies for regenerative medicine. In the CNS, direct lineage reprogramming of non-neuronal cells into clinically relevant neurons represents a highly innovative strategy to regenerate lost neurons for brain repair in several neurological disorders (for review see Heinrich et al., Nature Cell Biol, 2015). Along this line, we contributed important work by demonstrating that mouse astroglia can be directly reprogrammed in vitro to generate functional induced neurons (iNs) with different neurotransmitter identity (Heinrich et al., 2010; Heinrich et al., 2011). A major challenge was the translation of these findings obtained in the culture dish into the context of the adult brain in vivo. We showed that NG2 glia can be converted into iNs in the adult mouse cortex in vivo and following acute invasive injury (Heinrich et al., 2014).
Based on these studies our current research aims now at reprogramming glial cells residing within the injured brain -in pathological conditions- into functional iNs that:
|2016||18(3):396-409||Identification and Successful Negotiation of a Metabolic Checkpoint in Direct Neuronal Reprogramming||Gascon S, Murenu E, Masserdotti G, Ortega F, Russo GL, Petrik D, Deshpande A, Heinrich C, Karow M, Robertson SP, Schroeder T, Beckers J, Irmler M, Berndt C, Angeli JP, Conrad M, Berninger B, Götz M||Cell Stem Cell||-|
|2015||17(3):204-11||In vivo reprogramming for tissue repair||Heinrich C, Spagnoli FM, Berninger B||Nat Cell Biol||-|
|2014||3(6):1000-14||Sox2-mediated conversion of NG2 glia into induced neurons in the injured adult cerebral cortex||Heinrich C, Bergami M, Gascón S, Lepier A, Viganò F, Dimou L, Sutor B, Berninger B, Götz M||Stem Cell Reports||-|
|2013||12(4):426-39||Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog||Sirko S, Behrendt G, Johansson PA, Tripathi P, Costa M, Bek S, Heinrich C, Tiedt S, Colak D, Dichgans M, Fischer IR, Plesnila N, Staufenbiel M, Haass C, Snapyan M, Saghatelyan A, Tsai LH, Fischer A, Grobe K, Dimou L, Götz M||Cell Stem Cell||-|
|2012||11(4):471-6||Reprogramming of pericyte-derived cells of the adult human brain into induced neuronal cells||Karow M, Sánchez R, Schichor C, Masserdotti G, Ortega F, Heinrich C, Gascón S, Khan MA, Lie DC, Dellavalle A, Cossu G, Goldbrunner R, Götz M, Berninger B||Cell Stem Cell||-|
|2011||6(2):214-28||Generation of subtype-specific neurons from postnatal astroglia of the mouse cerebral cortex||Heinrich C, Gascón S, Masserdotti G, Lepier A, Sanchez R, Simon-Ebert T, Schroeder T, Götz M, Berninger B||Nat Protoc||-|
|2011||42(1):35-47||Increase in BDNF-mediated TrkB signaling promotes epileptogenesis in a mouse model of mesial temporal lobe epilepsy||Heinrich C, Lähteinen S, Suzuki F, Anne-Marie L, Huber S, Häussler U, Haas C, Larmet Y, Castren E, Depaulis A||Neurobiol Dis||-|
|2011||21(2):413-24||Neuronal network formation from reprogrammed early postnatal rat cortical glial cells||Blum R, Heinrich C, Sánchez R, Lepier A, Gundelfinger ED, Berninger B, Götz M||Cereb Cortex||-|
|2010||8(5):e1000373||Directing astroglia from the cerebral cortex into subtype specific functional neurons||Heinrich C, Blum R, Gascón S, Masserdotti G, Tripathi P, Sánchez R, Tiedt S, Schroeder T, Götz M, Berninger B||PLoS Biol||-|