Publication: Markers of senescence are often associated with neuronal differentiation in the developing sensory systems
Authors
Mera Rodríguez, José Antonio ; Álvarez Hernán, Guadalupe ; Gañán, Yolanda ; Solana Fajardo, Jorge ; Martín Partido, Gervasio ; Rodríguez León, Joaquín ; Francisco Morcillo, Javier
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
https://doi.org/10.14670/HH-18-549
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info:eu-repo/semantics/article
Description
Abstract
It has been shown that senescent cells
accumulate in transient structures of the embryo that
normally degenerate during tissue development. A
collection of biomarkers is generally accepted to define
senescence in embryonic tissues. The histochemical
detection of β-galactosidase activity at pH 6.0 (β-galpH6) is the most widely used assay for cellular
senescence. Immunohistochemical detection of common
mediators of senescence which block cell cycle
progression, including p16, p21, p63, p15 or p27, has
also been used to characterize senescent cells in the
embryo. However, the reliability of this techniques has
been discussed in recent publications because nonsenescent cells are also labelled during development.
Indeed, increased levels of senescent markers promote
differentiation over apoptosis in developing neurons,
suggesting that machinery used for the establishment of
cellular senescence is also involved in neuronal
maturation. Notably, it has recently been argued that a
comparable state of cellular senescence might be
adopted by terminally differentiated neurons. The
developing sensory systems provide excellent models for
studying if canonical markers of senescence are
associated with terminal neuronal differentiation.
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Citation
Histology and Histopathology, Vol.38, nº5, (2023)
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