Dr. rer. nat. Katja Stange
Forschungsinteressen
- Skelettmuskelentwicklung
- Physiologische Rolle myogener Zellen von Säugetieren
- Differenzierung myogener Vorläufer
- Möglichkeiten der Einflussnahme auf das Skelettmuskelwachstum
Lebenslauf
- 2015-heute: Postdoc am Leibniz Institut für Nutztierbiologie (FBN) Dummerstorf, Institut für Muskelbiologie und Wachstum
- 2015: Promotion zum Dr. rer. nat. an der Humboldt-Universität Berlin und Abschluss des Promotionsstudiums „Regenerative Therapien“ der Charité Universitätsmedizin Berlin
- 2012-2014: Doktorandenstipendiatin der Sonnenfeld-Stiftung
- 2011-2015: Promotionsstudium am Berlin Brandenburger Zentrum für Regenerative Therapien (BCRT), Modellsysteme für Zelldifferenzierung und Besuch der Berlin Brandenburg Schule für Regenerative Therapien (BSRT)
- 2011: Abschluss als Dipl.-Ing. der Technischen Universität Berlin
- 2005-2011: Studium der Medizinischen Biotechnologie an der Technischen Universität Berlin
Publikationen
Stange, K.; Schumacher, T.; Miersch, C.; Whelan, R.; Klünemann, M.; Röntgen, M. (2023):
Methionine Sources Differently Affect Production of Reactive Oxygen Species, Mitochondrial Bioenergetics, and Growth of Murine and Quail Myoblasts In Vitro. CURR ISSUES MOL BIOL
45 (4): 2661-2680
Stange, K.; Keric, A.; Friese, A.; Röntgen, M. (2022):
Preparation of spheroids from primary pig cells in a mid-scale bioreactor retaining their myogenic potential. Cells-Basel 11 (9): 1453, 1-18
Grunow, B.; Stange, K.; Bochert, R.; Tönißen, K. (2021):
Histological and biochemical evaluation of skeletal muscle in the two salmonid species Coregonus maraena and Oncorhynchus mykiss. Plos One 16: e0255062, 1-17
https://doi.org/10.1371/journal.pone.0255062
Zhao, Y.; Albrecht, E.; Stange, K.; Li, Z.; Schregel, J.; Sciascia, Q. L.; Metges, C. C.; Maak, S. (2021):
Glutamine supplementation stimulates cell proliferation in skeletal muscle and cultivated myogenic cells of low birth weight piglets. Sci Rep-UK 11: 13432, 1-15
https://doi.org/10.1038/s41598-021-92959-6
Stange, K.; Ahrens, H. E.; von Maltzahn, J.; Röntgen, M. (2020):
Isolation and ex vivo cultivation of single myofibers from porcine muscle. IN VITRO CELL DEV-AN 56 (8): 585-592
https://doi.org/10.1007/s11626-020-00492-z
Stange, K.; Miersch, C.; Sponder, G.; Röntgen, M. (2020):
Low birth weight influences the postnatal abundance and characteristics of satellite cell subpopulations in pigs. Sci Rep-UK 10: 6149, 1-14
https://doi.org/10.1038/s41598-020-62779-1
Hildebrand, L.; Schmidt-von Kegler, M.; Walther, M.; Seemann, P.; Stange, K. (2019):
Limb specific Acvr1-knockout during embryogenesis in mice exhibits great toe malformation as seen in Fibrodysplasia Ossificans Progressiva (FOP). Dev Dynam 248 (5): 396-403
https://doi.org/10.1002/dvdy.24
Miersch, C.; Stange, K.; Röntgen, M. (2018):
Effects of trypsinization and of a combined trypsin, collagenase, and DNase digestion on liberation and in vitro function of satellite cells isolated from juvenile porcine muscles. IN VITRO CELL DEV-AN 54 (6): 406-412
https://doi.org/10.1007/s11626-018-0263-5
Miersch, C.; Stange, K.; Röntgen, M. (2018):
Separation of functionally divergent muscle precursor cell populations from porcine juvenile muscles by discontinuous Percoll density gradient centrifugation. BMC Cell Biol 19: 2, 1-12
https://doi.org/10.1186/s12860-018-0156-1
Miersch, C.; Stange, K.; Hering, S.; Kolisek, M.; Viergutz, T.; Röntgen, M. (2017):
Molecular and functional heterogeneity of early postnatal porcine satellite cell populations is associated with bioenergetic profile. Sci Rep-UK 7: 45052, 1-14
https://dx.doi.org//10.1038/srep45052
Hildebrand, L.; Stange, K.; Deichsel, A.; Gossen, M.; Seemann, P. (2017):
The Fibrodysplasia Ossificans Progressiva (FOP) mutation p.R206H in ACVR1 confers an altered ligand response. CELL SIGNAL 29: 23-30
https://dx.doi.org/10.1016/j.cellsig.2016.10.001
Stange, K.; Ott, C.E.; Schmidt-von Kegler, M.; Gillesen-Kaesbach, G.; Mundlos, S.; Dathe, K.; Seemann, P. (2015):
Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?. J Hum Genet 60 (8): 419-425
https://dx.doi.org/10.1038/jhg.2015.48
Stange, K.; Désir, J.; Kakar, N.; Müller, T.D.; Budde, B.S.; Gordon, C.T.; Horn, D.; Seemann, P.; Borck, G. (2015):
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia. Orphanet J Rare Dis 10: 84, 1-6
https://dx.doi.org/10.1186/s13023-015-0299-5