Sten Eirik W. Jacobsen Lab (Hematopoietic Stem Cell Biology Group)
Unraveling normal and malignant hematopoietic stem and progenitor cell biology at the single cell level
Establishing the normal lineage commitment pathways from hematopoietic stem cells to lineage-restricted progenitors remains an important goal towards unravelling the regulation of blood lineage development, and how this is perturbed in hematological malignancies.
The Jacobsen Lab has for more than a decade had a focus on establishing key lineage commitment/restriction steps and blood lineage pathways in normal hematopoiesis (Adolfsson Cell 2005; Boiers Cell Stem Cell 2013; Sanjuan-Pla Nature 2013; Luis Nature Immunology 2016; Drissen Nature Immunology 2016; Carrelha Nature 2018). Distinct cancer stem cells (CSCs) might underlie relapses after complete remissions. The Jacobsen Lab has identified and characterized distinct and rare candidate CSCs and their therapeutic resistance in the chronic hematological malignancies myelodysplastic syndromes (MDS; Tehranchi New Engl J Med 2010; Woll Cancer Cell 2014) and myeloproliferative neoplasms (Mead N Engl J Med 2012; Giustacchini Nature Medicine 2017).
The current focus of the research program of the Jacobsen lab is to apply different genetic tools and functional as well as molecular single cell analysis to unravel the dynamics of stem and progenitor cells in unperturbed hematopoiesis as well as in response to distinct challenges, in mice as well as in normal human subjects. We also model the impact of recurrent genetic lesions at distinct stages of hematopoietic lineage commitment, to identify key cellular targets and molecular events in the transformation from normal to malignant hematopoiesis. In parallel we track the cellular fate and genetic evolution of clonal hematopoiesis in normal individuals as well as pre-leukemic and leukemic stem cells in patients during the natural course of hematopoietic malignancies and following treatment. Through these research directions we aim to identify novel therapeutic strategies towards regenerative hematopoiesis and targeting of leukemic stem cells.
|Sten Eirik W. Jacobsen||M.D. Ph.D., Professor, Group Leader|
|Dimitra Vasileiadi||M.Sc., Research Administrator/ Personal Assistant|
|Ellen Markljung||Ph.D., Senior Lab Manager|
|Kari Högstrand||Ph.D., Senior Lab Manager|
|Amy Hillen||M.Sc., Research Technician|
|Allegra Matheson Lord||Post doc|
|Edyta Wójtowicz||Post doc|
|Marios Dimitriou||Post doc|
|Laura Kettyle||Post doc|
|Karin Belander-Strålin||M.D. PhD student|
Hierarchically related lineage-restricted fates of multipotent haematopoietic stem cells.
Nature 2018 Feb;554(7690):106-111
Ezh2 and Runx1 Mutations Collaborate to Initiate Lympho-Myeloid Leukemia in Early Thymic Progenitors.
Cancer Cell 2018 Feb;33(2):274-291.e8
Single-cell transcriptomics uncovers distinct molecular signatures of stem cells in chronic myeloid leukemia.
Nat. Med. 2017 Jun;23(6):692-702
Initial seeding of the embryonic thymus by immune-restricted lympho-myeloid progenitors.
Nat. Immunol. 2016 Dec;17(12):1424-1435
Distinct myeloid progenitor-differentiation pathways identified through single-cell RNA sequencing.
Nat. Immunol. 2016 06;17(6):666-676
A dynamic niche provides Kit ligand in a stage-specific manner to the earliest thymocyte progenitors.
Nat. Cell Biol. 2016 Feb;18(2):157-67
Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo.
Cancer Cell 2014 Jun;25(6):794-808
Lymphomyeloid contribution of an immune-restricted progenitor emerging prior to definitive hematopoietic stem cells.
Cell Stem Cell 2013 Nov;13(5):535-48
Platelet-biased stem cells reside at the apex of the haematopoietic stem-cell hierarchy.
Nature 2013 Oct;502(7470):232-6
Germline JAK2 mutation in a family with hereditary thrombocytosis.
N. Engl. J. Med. 2012 Mar;366(10):967-9
The earliest thymic T cell progenitors sustain B cell and myeloid lineage potential.
Nat. Immunol. 2012 Feb;13(4):412-9
Persistent malignant stem cells in del(5q) myelodysplasia in remission.
N. Engl. J. Med. 2010 Sep;363(11):1025-37