👤 Karsten Köhler

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4
Articles
4
Name variants
Also published as: Ina Köhler, Lisa-Maria Köhler, Rolf Köhler
articles
Alexander Ewerling-Haehnel, Ina Köhler, Isa Graebling +6 more · 2025 · Scientific reports · Nature · added 2026-04-24
Cilia were one of the characteristic traits of the last eukaryotic common ancestor and are highly conserved among eukaryotes. Their proteomic makeup is remarkably similar throughout all eukaryotic lin Show more
Cilia were one of the characteristic traits of the last eukaryotic common ancestor and are highly conserved among eukaryotes. Their proteomic makeup is remarkably similar throughout all eukaryotic lineages. Recently, several ciliary transport proteins, namely the Bardet-Biedl Syndrome (BBS) proteins, were shown to traverse the nuclear envelope, and to modulate gene expression. Insects have been critically understudied in cilia biology since they only exhibit cilia on a subset of cells. We present evidence that the BBSome is largely conserved in multiple insect lineages. To examine BBS protein expression within insects, we profiled tissues, castes, and sexes of the honeybee Apis mellifera, a species where the genome encodes for multiple behavioural and morphological phenotypes. We find variation in expression profiles of putative BBSome-associated genes across different tissues, including those lacking cilia, indicating possible non-ciliary functions. We also demonstrate that expression of individual BBS proteins varies significantly between queens' and males' tissues, especially in neuronal tissue. Particularly high overexpression of BBS4 in glandular tissue indicates a cilia-independent role. Our findings provide evolutionary insight into the conservation of BBSome components across insects, suggesting potential additional roles for cilia proteins in non-ciliated tissues, providing candidate genes from diverse insect orders for future experimental work. Show less
📄 PDF DOI: 10.1038/s41598-025-19137-w
BBS4
Mikhail Feofanov, Gerrit Martin Daubner, Andrea Saltalamacchia +11 more · 2025 · Biochemistry and biophysics reports · Elsevier · added 2026-04-24
Replacing growth factors with a synthetic alternative molecule is an attractive opportunity to increase consistency, scalability, and cost-effectiveness of cell-based products. Herein, we describe the Show more
Replacing growth factors with a synthetic alternative molecule is an attractive opportunity to increase consistency, scalability, and cost-effectiveness of cell-based products. Herein, we describe the discovery of a chemical class of FGFR1 agonists that mimic the action of basic fibroblast growth factor (bFGF), an essential component of cell culture media. The guanylhydrazone-based molecule, TCB-32, was identified via structure-based virtual screening of the orthosteric binding site of FGFR1. It was shown to significantly increase cell proliferation by activating the FGFR1 signaling pathway like bFGF and exhibited enhanced thermostability over bFGF by retaining activity over the course of several days. After extensive structure-activity relationship studies, it was possible to increase potency and efficacy leading to three highly potent agonists. This finding has the potential to remove current bottlenecks in large-scale cell production, as required for applications such as cultivated meat or cell therapy. Show less
📄 PDF DOI: 10.1016/j.bbrep.2025.102167
FGFR1
Alexandra Niedermayer, Jana Stursberg, Anke Katharina Bergmann +9 more · 2025 · Leukemia · Nature · added 2026-04-24
📄 PDF DOI: 10.1038/s41375-025-02591-w
MLLT10
Tom Le Voyer, Sonoko Sakata, Miyuki Tsumura +44 more · 2021 · Journal of immunology (Baltimore, Md. : 1950) · added 2026-04-24
Autosomal recessive (AR) STAT1 deficiency is a severe inborn error of immunity disrupting cellular responses to type I, II, and III IFNs, and IL-27, and conferring a predisposition to both viral and m Show more
Autosomal recessive (AR) STAT1 deficiency is a severe inborn error of immunity disrupting cellular responses to type I, II, and III IFNs, and IL-27, and conferring a predisposition to both viral and mycobacterial infections. We report the genetic, immunological, and clinical features of an international cohort of 32 patients from 20 kindreds: 24 patients with complete deficiency, and 8 patients with partial deficiency. Twenty-four patients suffered from mycobacterial disease (bacillus Calmette-Guérin = 13, environmental mycobacteria = 10, or both in 1 patient). Fifty-four severe viral episodes occurred in sixteen patients, mainly caused by Show less
📄 PDF DOI: 10.4049/jimmunol.2001451
IL27