4.5 Article

The unfolded protein response regulator ATF6 promotes mesodermal differentiation

Journal

SCIENCE SIGNALING
Volume 11, Issue 517, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scisignal.aan5785

Keywords

-

Funding

  1. NIH [EY027335, NS088485, EY018213, EY024698, EY026682, AG050437, EY019007, CA013696, EY0223589, UL1TR001114, AG046495, R01EY025693]
  2. VA Merit awards [I01BX002284, I01RX002340]
  3. New York State [N09G-302, N13G-275]

Ask authors/readers for more resources

ATF6 encodes a transcription factor that is anchored in the endoplasmic reticulum (ER) and activated during the unfolded protein response (UPR) to protect cells from ER stress. Deletion of the isoform activating transcription factor 6 alpha (ATF6 alpha) and its paralog ATF6 beta results in embryonic lethality and notochord dysgenesis in nonhuman vertebrates, and loss-of-function mutations in ATF6 alpha are associated with malformed neuroretina and congenital vision loss in humans. These phenotypes implicate an essential role for ATF6 during vertebrate development. We investigated this hypothesis using human stem cells undergoing differentiation into multipotent germ layers, nascent tissues, and organs. We artificially activated ATF6 in stem cells with a small-molecule ATF6 agonist and, conversely, inhibited ATF6 using induced pluripotent stem cells from patients with ATF6 mutations. We found that ATF6 suppressed pluripotency, enhanced differentiation, and unexpectedly directed mesodermal cell fate. Our findings reveal a role for ATF6 during differentiation and identify a new strategy to generate mesodermal tissues through the modulation of the ATF6 arm of the UPR.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available