Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2014 Feb 18;5(1):24. doi: 10.1186/scrt413

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2014 Schröter et al.; licensee BioMed Central Ltd.

The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PMC Copyright notice

Scheme of the distinct proteasome-types present in murine and human pluripotent and differentiated cells. (A) An abundance of 30S proteasome is presented in mouse embryonic stem cells (mESCs) compared with 3-day differentiated ESCs. The PA28 complex is induced upon differentiation and anchored to the inducible proteasome complex.(B) Downregulated expression of the 30S complex upon neural progenitor cells (NPCs) and neuronal differentiation is found. In contrast to the human ESCs (hESCs), the neural cells have more free 20S complex. AGE, advanced glycation end product; iP, immunoproteasome; RP, regulatory particle.