Keratin-abhängige Regulation von Mitochondrien in Keratinozyten und in Mausepidermis
Zusammenfassung der Projektergebnisse
In this project, we investigated the role of keratins in mitochondrial dynamics and physiology, using keratinocytes which lack the entire keratin cytoskeleton following deletion of keratin gene clusters, in comparison to normal control an rescue cells that re-express a single keratin pair. In addition, we investigated the interplay of keratins and mitochondria in EBS and normal human keratinocytes. The comparative analysis of keratin-deficient and WT mouse keratinocytes and of human EBS and normal keratinocytes revealed a hitherto unknown role of keratins in mitochondrial positioning, dynamics and activity. In the absence of keratins, mitochondria were hyperfused. We showed that keratins modulate cellular redox homeostasis, which affects mitochondrial morphology and function partially via Drp1 translocation to mitochondria. This suggests that a crosstalk between keratins and mitochondria might adapt ROS signaling and metabolism to maintain epidermal integrity during tissue homeostasis, upon barrier defects, blistering skin disease and wounding. Our analysis of the EBS-associated K14R125C mutation revealed an impaired mitochondrial activity in primary and immortalized EBS keratinocytes which may be relevant for epidermal physiology, including barrier formation and diseases resulting in inflammation following barrier defects, such as atopic dermatitis.
Projektbezogene Publikationen (Auswahl)
- Lessons from Animal Models of Cytoplasmic Intermediate Filament Proteins. Subcell Biochem. 2017;82:171-230
Bouameur JE, Magin TM
(Siehe online unter https://doi.org/10.1007/978-3-319-49674-0_7) - Keratins Regulate p38MAPK-Dependent Desmoglein Binding Properties in Pemphigus. Front Immunol. 2018 Mar 19;9:528
Vielmuth F, Walter E, Fuchs M, Radeva MY, Buechau F, Magin TM, Spindler V, Waschke J
(Siehe online unter https://doi.org/10.3389/fimmu.2018.00528) - Mouse Keratinocytes Without Keratin Intermediate Filaments Demonstrate Substrate Stiffness Dependent Behaviors. Cell Mol Bioeng. 2018 May 2;11(3):163-174
Zarkoob H, Chinnathambi S, Halberg SA, Selby JC, Magin TM, Sander EA
(Siehe online unter https://doi.org/10.1007/s12195-018-0526-y) - Keratin defects trigger the itch- inducing cytokine thymic stromal lymphopoietin through amphiregulin-epidermal growth factor receptor signaling. J Allergy Clin Immunol. 2019 Dec;144(6):1719-1722.e3
Scheffschick A, Kiritsi D, Magin TM
(Siehe online unter https://doi.org/10.4014/jmb.1907.07011) - A dominant vimentin variant causes a rare syndrome with premature aging. Eur J Hum Genet. 2020 Sep;28(9):1218- 1230
Cogné B, Bouameur JE, Hayot G, Latypova X, Pattabiraman S, Caillaud A, Si-Tayeb K, Besnard T, Küry S, Chariau C, Gaignerie A, David L, Bordure P, Kaganovich D, Bézieau S, Golzio C, Magin TM, Isidor B
(Siehe online unter https://doi.org/10.1038/s41431-020-0583-2) - An intact keratin network is crucial for mechanical integrity and barrier function in keratinocyte cell sheets. Cell Mol Life Sci. 2020 Nov;77(21):4397-4411
Karsch S, Büchau F, Magin TM, Janshoff A
(Siehe online unter https://doi.org/10.1007/s00018-019-03424-7) - Disease-associated keratin mutations reduce traction forces and compromise adhesion and collective migration. J Cell Sci. 2020 Jul 29;133(14):jcs243956
Fujiwara S, Deguchi S, Magin TM
(Siehe online unter https://doi.org/10.1242/jcs.243956) - Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity. J Invest Dermatol. 2020 Jul;140(7):1438-1442.e5
Vetter A, Jahn K, Bouameur JE, Kiritsi D, Magin TM
(Siehe online unter https://doi.org/10.1016/j.jid.2019.10.023) - Epidermolysis bullosa. Nat Rev Dis Primers. 2020 Sep 24;6(1):78
Bardhan A, Bruckner-Tuderman L, Chapple ILC, Fine JD, Harper N, Has C, Magin TM, Marinkovich MP, Marshall JF, McGrath JA, Mellerio JE, Polson R, Heagerty AH
(Siehe online unter https://doi.org/10.1038/s41572-020-0210-0) - Old mitochondria accumulate in pachyonychia congenita. Br J Dermatol. 2020 Mar;182(3):529-530
Vetter A, Magin TM
(Siehe online unter https://doi.org/10.1111/bjd.18465)
