Scientists in the team of Marieke Essers and her doctoral student Simon Haas have now discovered an emergency program in mice that bypasses the known pathway of blood stem cell differentiation so that the vital thrombocytes are rapidly replenished. Dr. Essers is a research scientist at HI-STEM, the stem cell institute jointly sponsored by the German Cancer Research Center and the Dietmar Hopp Foundation.
Essers and her co-workers have discovered, within the hematopoietic stem cells, a small cell population that is defined molecularly to induce differentiation of megakaryocytes, the progenitors of platelets. This population of quiescent stem cells does not provide the normal supply of platelets but serves as an emergency backup.
When quiescent, these cells express only few proteins. In the event of an acute infection, they are aroused from their quiescent state by the messenger substance interferon α, express the typical megakaryocyte proteins and are rapidly differentiated into advanced precursor cells. This emergency system rapidly replaces the thrombocytes that were lost as a result of the infection.
This elegant emergency backup bypasses the lengthy process of normal hematopoietic cell differentiation, thereby ensuring that any life-threatening loss of thrombocytes is compensated for quickly. However, repeated infections can result in the reservoir of emergency stem cells being depleted.
Simon Haas, Jenny Hansson, Daniel Klimmeck, Dirk Loeffler, Lars Velten, Hannah Uckelmann, Stephan Wurzer, Áine M. Prendergast, Alexandra Schnell, Klaus Hexel, Rachel Santarella-Mellwig, Sandra Blaszkiewicz, Andrea Kuck, Hartmut Geiger, Michael D. Milsom, Lars M. Steinmetz, Timm Schroeder, Andreas Trumpp, Jeroen Krijgsveld, Marieke A. G. Essers: Inflammation-induced Emergency Megakaryopoiesis Driven by Hematopoietic Stem Cell-like Megakaryocyte Progenitors. Cell Stem Cell 2015, 10.1016/j.stem.2014.07.005