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Koenigs-Werner, H.

Publications and source records attributed to Koenigs-Werner, H..

2 recordsLinked to original sources

Differential behavior of pericytes and adipose stromal cells in vasculogenesis and angiogenesis

The pericyte is a key player in vascularization, protecting endothelial cells from external harm and promoting formation of new vessels and connections when necessary. However, pericytic identity and its relation with other cell types, such as the mesenchymal stromal/stem cells, is highly debated. To compare the behaviour of pericytes and unselected stromal cells in vascularization, we used multichannel microfluidic chips to replicate the two processes of vessel formation: vasculogenesis, the de novo vessel formation, and angiogenesis, the sprouting of new vessels from existing ones. In angiogenesis, pericytes promote significantly more and longer sproutings than stromal cells. In vasculogenesis, stromal cells promote the formation of structures ressembling the embryonic capillary plexus, whereas pericytes wrap around the endothelial cells, arresting their division and forcing them into tubulogenesis. Whole-transcriptome sequencing confirms an upregulation of pro-vascularization and cytostatic genes in co-cultures of pericytes and endothelial cells; while stromal cells strongly stimulate mitosis and organelle biogenesis pathways and decrease the release of pro-inflammatory cytokines. In this study, we offer new insights into the pericyte-endothelial cell relation and the mesenchymal stromal cell elusive identity, relevant in both vascular biology and tissue engineering.

cell biology↗

Transformation of primary murine peritoneal mast cells by constitutive KIT activation as a result of lost Cdkn2a/Arf expression

Mast cells (MCs) are immune cells of the myeloid lineage distributed in tissues throughout the body. Phenotypically, they are a heterogeneous group characterized by different protease repertoires stored in secretory granules and differential presence of receptors. To adequately address aspects of MC biology either primary MCs isolated from human or mouse tissue or different human MC lines, like HMC-1.1 and -1.2, or rodent MC lines like L138.8A or RBL-2H3 are frequently used. Nevertheless, cellular systems to study MC functions are very limited. We have generated a murine connective tissue-like MC line, termed PMC-306, derived from primary peritoneal MCs (PMCs), which spontaneously transformed. We analyzed PMC-306 cells regarding MC surface receptor expression, effector functions and respective signaling pathways, and found that the cells reacted very similar to primary wildtype (WT) PMCs. In this regard, stimulation with MAS-related G-protein-coupled receptor member B2 (MRGPRB2) ligands induced respective signaling and effector functions. Furthermore, PMC-306 cells revealed significantly accelerated cell cycle progression, which however was still dependent on IL-3 and stem cell factor (SCF). Phenotypically, PMC-306 cells adopted an immature connective tissue-like MCs appearance. The reason for immortalization most likely is the loss of the two critical cell cycle regulators Cdkn2a/INK4A and Arf/p19, respectively. The loss of Cdkn2a and Arf expression could be mimicked in primary bone marrow-derived mast cells (BMMCs) by SCF supplementation strongly arguing for an involvement of KIT activation in the transformation process. Hence, this new cell line might be a useful tool to study further aspects of PMC function and to address tumorigenic processes associated with MC leukemia.

immunology↗