René Krüger

ORCID: 0000-0003-3731-0224
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About
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Research Areas
  • Renal Diseases and Glomerulopathies
  • 3D Printing in Biomedical Research
  • Renal and related cancers
  • Renal cell carcinoma treatment
  • Cancer Cells and Metastasis
  • Genetic and Kidney Cyst Diseases
  • Cellular Mechanics and Interactions
  • Epigenetics and DNA Methylation
  • Cancer, Hypoxia, and Metabolism
  • Chronic Kidney Disease and Diabetes
  • Receptor Mechanisms and Signaling
  • Birth, Development, and Health
  • Immune cells in cancer
  • Genetic Associations and Epidemiology
  • Ion Transport and Channel Regulation
  • Multiple Myeloma Research and Treatments
  • MRI in cancer diagnosis
  • Neonatal Respiratory Health Research
  • Inflammasome and immune disorders
  • Protein Degradation and Inhibitors
  • Glycosylation and Glycoproteins Research
  • Single-cell and spatial transcriptomics
  • Diabetes Treatment and Management
  • Nuclear Structure and Function
  • Ubiquitin and proteasome pathways

Universitätsklinikum Erlangen
2021-2025

Friedrich-Alexander-Universität Erlangen-Nürnberg
2021-2024

RELX Group (United States)
2023

Abstract Biofabrication techniques enable the performance of bioinspired three‐dimensional (3D) matrices resembling primary tumors. To validate their reliability, embedded cells may express complex biophysical responses. Among others, emergence tumor heterogeneity and generation Polyploid Giant Cancer Cells (PGCC), as a result mechanical stress, are two most challenging hallmarks to resemble in vitro. Here, these phenomena studied cultured on two‐dimensional (2D) flasks, 3D spheroids, or...

10.1002/adfm.202311139 article EN cc-by-nc Advanced Functional Materials 2024-02-10

Evolution of clear cell renal carcinoma is guided by dysregulation hypoxia-inducible transcription factor (HIF) pathways following loss the von Hippel-Lindau tumor suppressor protein. Renal (RCC)-associated polymorphisms influence HIF-DNA interactions at enhancers important oncogenes thereby modulating risk developing cancer. A strong signal genome-wide association with RCC was determined for single nucleotide polymorphism (SNP) rs4903064, located on chr14q.24.2 within an intron DPF3,...

10.1016/j.jbc.2022.101699 article EN cc-by-nc-nd Journal of Biological Chemistry 2022-02-08

Individuals of African ancestry carrying two pathogenic variants apolipoprotein 1 (APOL1) have a substantially increased risk for developing chronic kidney disease. The course APOL1 nephropathy is extremely heterogeneous and shaped by systemic factors such as response to interferon. However, additional environmental operating in this second-hit model been less well defined. Here, we reveal that stabilization hypoxia-inducible transcription (HIF) hypoxia or HIF prolyl hydroxylase inhibitors...

10.1016/j.kint.2023.03.035 article EN cc-by-nc-nd Kidney International 2023-04-23

Signaling-pathway analyses and the investigation of gene responses to different stimuli are usually performed in 2D monocultures. However, within glomerulus, cells grow 3D involved direct paracrine interactions with glomerular cell types. Thus, results from monoculture experiments must be taken caution. We cultured endothelial cells, podocytes mesangial 2D/3D monocultures co-cultures analyzed survival, self-assembly, expression, cell-cell interaction, pathways using live/dead assay,...

10.3390/ijms241210384 article EN International Journal of Molecular Sciences 2023-06-20

Podocytes are critical components of the glomerular filtration barrier, sitting on outside basement membrane. Primary and secondary foot processes characteristic for podocytes, but cell that develop in culture were not studied much past. Moreover, protocols diverse visualization methods mostly can only be used one technique, due to differences fixation, drying handling. However, we detected by single-cell RNA sequencing (scRNAseq) analysis cells reveal high variability genes involved...

10.3390/cells12091245 article EN cc-by Cells 2023-04-25

Objective We have recently shown that priming of synovial fibroblasts (SFs) drives arthritis flares. Pathogenic SFs is essentially mediated by epigenetic reprogramming. Bromodomain and extraterminal motif (BET) proteins translate changes into transcription. Here, we used a BET inhibitor (I‐BET151) to target inflammatory tissue reduce flare severity in murine experimental model. Methods BALB/c mice were treated intraperitoneal injection or local the paw with I‐BET151, which blocks interaction...

10.1002/art.42378 article EN cc-by-nc Arthritis & Rheumatology 2022-10-17

Abstract In this work, we studied the generation and rising of polyploid cancer cells as a product mechanical stress. To purpose, MCF7 breast were cultured on 2D ( i.e . flasks, or flat hydrogels), in 3D milieus Spheroids, immobilized within alginate-gelatin microbeads, named work tumor-like microcapsules), further analyzed by biophysical genetic methods (i.e. single-cell Traction Force Microscopy RNA-seq respectively). Our results show that preconditioned onto surfaces exhibit low number...

10.1101/2022.09.22.508846 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-09-23

Mutations in polycystin-1 which is encoded by the PKD1 gene are main causes for development of autosomal dominant polycystic kidney disease. However, only little known about physiological function and even less regulation its expression. Here, we show that expression induced hypoxia compounds stabilize hypoxia-inducible transcription factor (HIF) 1 α primary human tubular epithelial cells. Knockdown HIF subunits confirms HIF-1α-dependent Furthermore, ChIP-seq reveals interacts with a...

10.1098/rsos.220992 article EN cc-by Royal Society Open Science 2023-05-01

The interplay between genetic and environmental factors influences the course of chronic kidney disease (CKD). In this context, alterations in gene MUC1 (Mucin1) predispose to development CKD. These variations comprise polymorphism rs4072037, which alters splicing mRNA, length a region with variable number tandem repeats (VNTR), rare autosomal-dominant inherited dominant-negative mutations or 5' VNTR that causes autosomal dominant tubulointerstitial (ADTKD-MUC1). As hypoxia plays pivotal...

10.26508/lsa.202302078 article EN cc-by Life Science Alliance 2023-06-14

Abstract Background Genome-wide association studies (GWAS) have identified hundreds of genetic loci associated with kidney function. By combining these findings post-GWAS information (e.g., statistical fine-mapping to identify independent signals and narrow down causal variants; or different sources annotation data), new hypotheses regarding physiology disease aetiology can be obtained. These need tested in laboratory experiments, for example, therapeutic targets. For this purpose, the...

10.1186/s12859-023-05472-0 article EN cc-by BMC Bioinformatics 2023-09-21

Uncovering the function of understudied G protein-coupled receptors (GPCRs) provides a wealth untapped therapeutic potential. The poorly understood adhesion GPCR Gpr126 (Adgrg6) is widely expressed in developing kidneys. In adulthood, expression enriched parietal epithelial cells (PECs) and collecting duct urothelium. Whether plays role kidney disease remains unclear. Here, we characterized diseased kidneys mice, rats, humans. RT-PCR data show that altered disease. A quantitative RNAscope®...

10.3390/cells13100874 article EN cc-by Cells 2024-05-18

Abstract Background and Aims Podocytes typically represent a distinct morphology with long, interdigitating primary secondary foot processes wrapping around glomerular capillaries forming the filtration unit of kidney. In diseases like genetic focal segmental glomerulosclerosis (FSGS), podocyte alterations are often related to dysfunction barrier development proteinuria. Genetic mutations in relevant genes, important for process or actin cytoskeleton dynamics, known induce severe injury....

10.1093/ndt/gfad063c_5919 article EN Nephrology Dialysis Transplantation 2023-06-01
Gerhard Malnic Adriana Castello Costa Girardi Rolf A.K. Stahl Elion Hoxha William Couser and 95 more Tobias B. Huber Caroline Stigant Katherine A. Barraclough Mark Harber Nigel S. Kanagasundaram Charu Malik Vivekanand Jha Raymond Open Reiko Inagi Kentaro Yoshioka Mark R. Hanudel Mark J. Koury Volker H. Haase Chunni Lu A. Richard Kitching Roger G. Evans Paola Romagnani Laura Barisoni Masaomi Nangaku Peter Boor Alessia Fornoni Jürgen Floege P Coates Jonathan Himmelfarb Rachel Lennon Hans‐Joachim Anders Benjamin D. Humphreys Fergus Caskey Agnes B. Fogo M. Ben Hmida Tahar Mechichi Giorgina Barbara Piccoli Mohamed Ksibi Steffen Grampp René Krüger Victoria Lauer Sebastian Uebel Karl X. Knaup Julia Naas Verena Höffken Thomas Weide Mario Schiffer Stephanie Naas Johannes Schödel Violante Olivari Simona Maria Di Modica Maria Rosa Lidonnici Mariam Aghajan Celia Cordero-Sánchez Emanuele Tanzi Mariateresa Pettinato Alessia Pagani Francesca Tiboni Laura Silvestri Shuling Guo Giuliana Ferrari Antonella Nai Georg R. Herrnstadt Christoph B. Niehus Torben Ramcke Julia Hagenstein Laura-Isabell Ehnold Anna Nosko Matthias T. Warkotsch Frederic C. Feindt Simon Melderis Hans‐Joachim Paust Varshi Sivayoganathan Saskia-Larissa Jauch-Speer Milagros N. Wong Daniela Indenbirken Christian Krebs Ulf Panzer Victor G. Puelles Malte A. Kluger Oliver M. Steinmetz Tobias Sieckmann Gunnar Schley Neslihan Ögel Simon Kelterborn Felix Boivin Michael Fähling Muhammad Ashraf Martin Reichel Emilia Vigolo Andrea Hartner Falk‐Bach Lichtenberger Tilman Breiderhoff Felix Knauf Christian Rosenberger Felix Aigner Kai M. Schmidt‐Ott Holger Scholz Karin M. Kirschner Wenbin Liu

10.1016/s0085-2538(23)00349-6 article EN Kidney International 2023-06-20

Universitatsklinikum Erlangen Medizinische Klinik 4 Nephrologie und Hypertensiologie, Erlangen, Germany.

10.1681/asn.20213210s1191c article DE Journal of the American Society of Nephrology 2021-10-01
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