Multiplexed and single cell tracing of lipid metabolism

2019 ◽  
Vol 16 (11) ◽  
pp. 1123-1130 ◽  
Author(s):  
Christoph Thiele ◽  
Klaus Wunderling ◽  
Philipp Leyendecker
2020 ◽  
Vol 78 (5) ◽  
pp. 915-925.e7 ◽  
Author(s):  
Poonam Bheda ◽  
Diana Aguilar-Gómez ◽  
Nils B. Becker ◽  
Johannes Becker ◽  
Emmanouil Stavrou ◽  
...  
Keyword(s):  

2009 ◽  
Vol 113 (18) ◽  
pp. 6511-6519 ◽  
Author(s):  
Valentin Lulevich ◽  
Yi-Ping Shih ◽  
Su Hao Lo ◽  
Gang-yu Liu

2017 ◽  
Vol 102 (6) ◽  
pp. 2029-2038 ◽  
Author(s):  
Meghan L. Ruebel ◽  
Matthew Cotter ◽  
Clark R. Sims ◽  
Dean M. Moutos ◽  
Thomas M. Badger ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Raquel Rouco ◽  
Olimpia Bompadre ◽  
Antonella Rauseo ◽  
Olivier Fazio ◽  
Rodrigue Peraldi ◽  
...  

AbstractDevelopmental genes are frequently controlled by multiple enhancers sharing similar specificities. As a result, deletions of such regulatory elements have often failed to reveal their full function. Here, we use the Pitx1 testbed locus to characterize in detail the regulatory and cellular identity alterations following the deletion of one of its enhancers (Pen). By combining single cell transcriptomics and an in-embryo cell tracing approach, we observe an increased fraction of Pitx1 non/low-expressing cells and a decreased fraction of Pitx1 high-expressing cells. We find that the over-representation of Pitx1 non/low-expressing cells originates from a failure of the Pitx1 locus to coordinate enhancer activities and 3D chromatin changes. This locus mis-activation induces a localized heterochrony and a concurrent loss of irregular connective tissue, eventually leading to a clubfoot phenotype. This data suggests that, in some cases, redundant enhancers may be used to locally enforce a robust activation of their host regulatory landscapes.


2020 ◽  
Author(s):  
Jiurong Liang ◽  
Guanling Huang ◽  
Xue Liu ◽  
Forough Taghavifar ◽  
Ningshan Liu ◽  
...  

ABSTRACTAging is a critical risk factor in progressive lung fibrotic diseases such as idiopathic pulmonary fibrosis (IPF). Loss of integrity of type 2 alveolar epithelial cells (AEC2s) is the main causal event in the pathogenesis of IPF. To systematically examine the genomic program changes of AEC2s with aging and lung injury, we performed unbiased single cell RNA-seq analyses of lung epithelial cells from either uninjured or bleomycin-injured young and old mice. Major lung epithelial cell types were readily identified with canonical cell markers in our dataset. Heterogenecity of AEC2s was apparent, and AEC2s were then classified into three subsets according to their gene signatures. Genes related to lipid metabolism and glycolysis were significantly altered within these three clusters of AEC2s, and also affected by aging and lung injury. Importantly, IPF AEC2s showed similar genomic programming and metabolic changes as that of AEC2s from bleomycin injured old mouse lungs relative to controls. Furthermore, perturbation of both lipid metabolism and glycolysis significantly changed progenitor renewal capacity in 3-Demensional organoid culture of AEC2s. Taken togather, this work identified metabolic defects of AEC2s in aging and during lung injury. Strategies to rectify these altered programs would promote AEC2 renewal which in turn improves lung repair.One sentence summaryMetabolic defects of alveolar progenitors in aging and during lung injury impair their renewal.


Author(s):  
Cheng-Yu Fan ◽  
Tsai Chia-Jung ◽  
Lin Hsuan-Chao ◽  
Yu Ling-Yea ◽  
Hsiao Yung-Jen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document