Mania Ackermann

Dr. Mania Ackermann

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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2015 in Stem Cell Reports
Verified
Journal Article
Open access
NLNico Lachmann
Nico Lachmann
MAMania Ackermann
Mania Ackermann
EFEileen Frenzel
Eileen Frenzel
SLSteffi Liebhaber
Steffi Liebhaber
SBSebastian Brennig
Sebastian Brennig
TMThomas Moritz
Thomas Moritz
Interleukin-3 (IL-3) is capable of supporting the proliferation of a broad range of hematopoietic cell types, whereas granulocyte colony-stimulating factor (G-CSF) and macrophage CSF (M-CSF) represent critical cytokines in myeloid differentiation. When this was investigated in a pluripotent-stem-cell-based hematopoietic differentiation model, IL-3/G-CSF or IL-3/M-CSF exposure resulted in the continuous generation of myeloid cells from an intermediate myeloid-cell-forming complex containing CD34(+) clonogenic progenitor cells for more than 2 months. Whereas IL-3/G-CSF directed differentiation toward CD45(+)CD11b(+)CD15(+)CD16(+)CD66b(+) granulocytic cells of various differentiation stages up to a segmented morphology displaying the capacity of cytokine-directed migration, respiratory burst response, and neutrophil-extracellular-trap formation, exposure to IL-3/M-CSF resulted in CD45(+)CD11b(+)CD14(+)CD163(+)CD68(+) monocyte/macrophage-type cells capable of phagocytosis and cytokine secretion. Hence, we show here that myeloid specification of human pluripotent stem cells by IL-3/G-CSF or IL-3/M-CSF allows for prolonged and large-scale production of myeloid cells, and thus is suited for cell-fate and disease-modeling studies as well as gene- and cell-therapy applications.

30 November 2018 in Nature Communications
Verified
Journal Article
Open access
PDF file
MAMania Ackermann
Mania Ackermann
HKHenning Kempf
Henning Kempf
MHMiriam Hetzel
Miriam Hetzel
CHChristina Hesse
Christina Hesse
AHAnna Rafiei Hashtchin
Anna Rafiei Hashtchin
NLNico Lachmann
Nico Lachmann
The increasing number of severe infections with multi-drug-resistant pathogens worldwide highlights the need for alternative treatment options. Given the pivotal role of phagocytes and especially alveolar macrophages in pulmonary immunity, we introduce a new, cell-based treatment strategy to target bacterial airway infections. Here we show that the mass production of therapeutic phagocytes from induced pluripotent stem cells (iPSC) in industry-compatible, stirred-tank bioreactors is feasible. Bioreactor-derived iPSC-macrophages (iPSC-Mac) represent a highly pure population of CD45 + CD11b + CD14 + CD163 + cells, and share important phenotypic, functional and transcriptional hallmarks with professional phagocytes, however with a distinct transcriptome signature similar to primitive macrophages. Most importantly, bioreactor-derived iPSC-Mac rescue mice from Pseudomonas aeruginosa -mediated acute infections of the lower respiratory tract within 4-8 h post intra-pulmonary transplantation and reduce bacterial load. Generation of specific immune-cells from iPSC-sources in scalable stirred-tank bioreactors can extend the field of immunotherapy towards bacterial infections, and may allow for further innovative cell-based treatment strategies.

20 August 2014 in Science Translational Medicine
Verified
Journal Article
Closed access
PDF file
CHChristine Happle
Christine Happle
NLNico Lachmann
Nico Lachmann
Jelena SkuljecJelena Skuljec
Jelena Skuljec
MWMartin Wetzke
Martin Wetzke
MAMania Ackermann
Mania Ackermann
GHGesine Hansen
Gesine Hansen
Macrophage progenitors are an effective and long-lasting therapy of hereditary pulmonary alveolar proteinosis.

15 January 2014 in American Journal of Respiratory and Critical Care Medicine
Verified
Journal Article
Closed access
NLNico Lachmann
Nico Lachmann
CHChristine Happle
Christine Happle
MAMania Ackermann
Mania Ackermann
DLDoreen Lüttge
Doreen Lüttge
MWMartin Wetzke
Martin Wetzke
TMThomas Moritz
Thomas Moritz
Rationale: Hereditary pulmonary alveolar proteinosis (hPAP) caused by granulocyte–macrophage colony–stimulating factor (GM-CSF) receptor α-chain (CSF2RA) deficiency is a rare, life-threatening lung disease characterized by accumulation of proteins and phospholipids in the alveolar spaces. The disease is caused by a functional insufficiency of alveolar macrophages, which require GM-CSF signaling for terminal differentiation and effective degradation of alveolar proteins and phospholipids. Therapeutic options are extremely limited, and the pathophysiology underlying the defective protein degradation in hPAP alveolar macrophages remains poorly understood. Objectives: To further elucidate the cellular mechanisms underlying hPAP and evaluate novel therapeutic strategies, we here investigated the potential of hPAP patient-derived induced pluripotent stem cell (PAP-iPSCs) derived monocytes and macrophages. Methods: Patient-specific PAP-iPSCs were generated from CD34+ bone marrow cells of a CSF2RA-deficient patient with PAP. We assessed pluripotency, chromosomal integrity, and genetic correction of established iPSC lines. On hematopoietic differentiation, genetically corrected or noncorrected monocytes and macrophages were investigated in GM-CSF–dependent assays. Measurements and Main Results: Although monocytes and macrophages differentiated from noncorrected PAP-iPSCs exhibited distinct defects in GM-CSF–dependent functions, such as perturbed CD11b activation, phagocytic activity, and STAT5 phosphorylation after GM-CSF exposure and lack of GM-CSF uptake, these defects were fully repaired on lentiviral gene transfer of a codon-optimized CSF2RA-cDNA. Conclusions: These data establish PAP-iPSC–derived monocytes and macrophages as a valid in vitro disease model of CSF2RA-deficient PAP, and introduce gene-corrected iPSC-derived monocytes and macrophages as a potential autologous cell source for innovative therapeutic strategies. Transplantation of such cells to patients with hPAP could serve as a paradigmatic proof for the potential of iPSC-derived cells in clinical gene therapy.

17 January 2022 in Nature Protocols
Verified
Journal Article
Closed access
PDF file
MAMania Ackermann
Mania Ackermann
AHAnna Rafiei Hashtchin
Anna Rafiei Hashtchin
FMFelix Manstein
Felix Manstein
MOMarco Carvalho Oliveira
Marco Carvalho Oliveira
HKHenning Kempf
Henning Kempf
NLNico Lachmann
Nico Lachmann

14 July 2015 in EMBO Molecular Medicine
Verified
Journal Article
Open access
PDF file
MAMania Ackermann
Mania Ackermann
SLSteffi Liebhaber
Steffi Liebhaber
JKJan‐Henning Klusmann
Jan‐Henning Klusmann
NLNico Lachmann
Nico Lachmann
Pluripotent stem cells (PSCs) such as embryonic stem cells or induced pluripotent stem cells represent a promising cell type to gain novel insights into human biology. Understanding the differentiation process of PSCs in vitro may allow for the identification of cell extrinsic/intrinsic factors, driving the specification process toward all cell types of the three germ layers, which may be similar to the human in vivo scenario. This would not only lay the ground for an improved understanding of human embryonic development but would also contribute toward the generation of novel cell types used in cell replacement therapies. In this line, especially the developmental process of mesodermal cells toward the hematopoietic lineage is of great interest. Therefore, this review highlights recent progress in the field of hematopoietic specification of pluripotent stem cell sources. In addition, we would like to shed light on emerging factors controlling primitive and definitive hematopoietic development and to highlight recent approaches to improve the differentiation potential of PSC sources toward hematopoietic stem/progenitor cells. While the generation of fully defined hematopoietic stem cells from PSCs remains challenging in vitro , we here underline the instructive role of cell extrinsic factors such as cytokines for the generation of PSC‐derived mature hematopoietic cells. Thus, we have comprehensively examined the role of cytokines for the derivation of mature hematopoietic cell types such as macrophages, granulocytes, megakaryocytes, erythrocytes, dendritic cells, and cells of the B‐ and T‐cell lineage.