Deficiency in Retinal TGF beta Signaling Aggravates Neurodegeneration by Modulating Pro-Apoptotic and MAP Kinase Pathways

Bielmeier, Christina B. and Schmitt, Sabrina and Kleefeldt, Nikolai and Boneva, Stefaniya K. and Schlecht, Anja and Vallon, Mario and Tamm, Ernst R. and Hillenkamp, Jost and Ergün, Süleyman and Neueder, Andreas and Braunger, Barbara M. (2022) Deficiency in Retinal TGF beta Signaling Aggravates Neurodegeneration by Modulating Pro-Apoptotic and MAP Kinase Pathways. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (5): 2626. ISSN 1422-0067

Full text not available from this repository.

Abstract

Transforming growth factor beta (TGF beta) signaling has manifold functions such as regulation of cell growth, differentiation, migration, and apoptosis. Moreover, there is increasing evidence that it also acts in a neuroprotective manner. We recently showed that TGF beta receptor type 2 (Tgfbr2) is upregulated in retinal neurons and Muller cells during retinal degeneration. In this study we investigated if this upregulation of TGF beta signaling would have functional consequences in protecting retinal neurons. To this end, we analyzed the impact of TGF beta signaling on photoreceptor viability using mice with cell type-specific deletion of Tgfbr2 in retinal neurons and Muller cells (Tgfbr2(& UDelta;OC)) in combination with a genetic model of photoreceptor degeneration (VPP). We examined retinal morphology and the degree of photoreceptor degeneration, as well as alterations of the retinal transcriptome. In summary, retinal morphology was not altered due to TGF beta signaling deficiency. In contrast, VPP-induced photoreceptor degeneration was drastically exacerbated in double mutant mice (Tgfbr2(& UDelta;OC); VPP) by induction of pro-apoptotic genes and dysregulation of the MAP kinase pathway. Therefore, TGF beta signaling in retinal neurons and Muller cells exhibits a neuroprotective effect and might pose promising therapeutic options to attenuate photoreceptor degeneration in humans.

Item Type: Article
Uncontrolled Keywords: RETINITIS-PIGMENTOSA; USHER-SYNDROME; MYOSIN VIIA; MECHANISMS; EXPRESSION; NEURONS; REACTIVITY; RECEPTOR; FATE; FOS; TGF beta signaling; retina; retinitis pigmentosa; MAP kinase pathway; ferroptosis; neuro-/photoreceptor degeneration
Subjects: 500 Science > 570 Life sciences
600 Technology > 610 Medical sciences Medicine
Divisions: Biology, Preclinical Medicine > Institut für Anatomie > Lehrstuhl für Humananatomie und Embryologie > Prof. Dr. Ernst Tamm
Depositing User: Dr. Gernot Deinzer
Date Deposited: 16 Feb 2024 10:22
Last Modified: 16 Feb 2024 10:22
URI: https://pred.uni-regensburg.de/id/eprint/58057

Actions (login required)

View Item View Item