Elimination of damaged proteins during differentiation of embryonic stem cells.

Abstract:

:During mammalian aging, cellular proteins become increasingly damaged: for example, by carbonylation and formation of advanced glycation end products (AGEs). The means to ensure that offspring are born without such damage are unknown. Unexpectedly, we found that undifferentiated mouse ES cells contain high levels of both carbonyls and AGEs. The damaged proteins, identified as chaperones and proteins of the cytoskeleton, are the main targets for protein oxidation in aged tissues. However, the mouse ES cells rid themselves of such damage upon differentiation in vitro. This elimination of damaged proteins coincides with a considerably elevated activity of the 20S proteasome. Moreover, damaged proteins were primarily observed in the inner cell mass of blastocysts, whereas the cells that had embarked on differentiation into the trophectoderm displayed drastically reduced levels of protein damage. Thus, the elimination of protein damage occurs also during normal embryonic development in vivo. This clear-out of damaged proteins may be a part of a previously unknown rejuvenation process at the protein level that occurs at a distinct stage during early embryonic development.

authors

Hernebring M,Brolén G,Aguilaniu H,Semb H,Nyström T

doi

10.1073/pnas.0510944103

subject

Has Abstract

pub_date

2006-05-16 00:00:00

pages

7700-5

issue

20

eissn

0027-8424

issn

1091-6490

pii

0510944103

journal_volume

103

pub_type

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