Igf signaling couples retina growth with body growth by modulating progenitor cell division

How the body and organs balance their relative growth is of key importance for coordinating size and function. This is of particular relevance in organisms, which continue to grow over their entire life span. We addressed this issue in the neuroretina of medaka fish (Oryzias latipes), a well-studied...

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Hauptverfasser: Becker, Clara (VerfasserIn) , Lust, Katharina (VerfasserIn) , Wittbrodt, Joachim (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 15 April 2021
In: Development
Year: 2021, Jahrgang: 148, Heft: 7, Pages: 1-13
ISSN:1477-9129
DOI:10.1242/dev.199133
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1242/dev.199133
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Verfasserangaben:Clara Becker, Katharina Lust and Joachim Wittbrodt
Beschreibung
Zusammenfassung:How the body and organs balance their relative growth is of key importance for coordinating size and function. This is of particular relevance in organisms, which continue to grow over their entire life span. We addressed this issue in the neuroretina of medaka fish (Oryzias latipes), a well-studied system with which to address vertebrate organ growth. We reveal that a central growth regulator, Igf1 receptor (Igf1r), is necessary and sufficient for proliferation control in the postembryonic retinal stem cell niche: the ciliary marginal zone (CMZ). Targeted activation of Igf1r signaling in the CMZ uncouples neuroretina growth from body size control, and we demonstrate that Igf1r operates on progenitor cells, stimulating their proliferation. Activation of Igf1r signaling increases retinal size while preserving its structural integrity, revealing a modular organization in which progenitor differentiation and neurogenesis are self-organized and highly regulated. Our findings position Igf signaling as a key module for controlling retinal size and composition, with important evolutionary implications.
Beschreibung:Gesehen am 29.07.2021
Beschreibung:Online Resource
ISSN:1477-9129
DOI:10.1242/dev.199133