The pivotal protein profile between the conjoined twins and normal mosquitofish Gambusia affinis based on iTRAQ proteomic analysis

Author(s):  
Lanfen Fan ◽  
Lei Wang ◽  
Hui Guo ◽  
Jixing Zou
2015 ◽  
Vol 14 (2) ◽  
pp. 5970-5978 ◽  
Author(s):  
Y. Zhao ◽  
Y. Zhang ◽  
H.B. Song ◽  
F. Wu ◽  
X.L. Wang ◽  
...  

Cells ◽  
2019 ◽  
Vol 8 (9) ◽  
pp. 1087 ◽  
Author(s):  
Bonafede ◽  
Brandi ◽  
Manfredi ◽  
Scambi ◽  
Schiaffino ◽  
...  

Stem cell therapy represents a promising approach in the treatment of several neurodegenerative disorders, including amyotrophic lateral sclerosis (ALS). The beneficial effect of stem cells is exerted by paracrine mediators, as exosomes, suggesting a possible potential use of these extracellular vesicles as non-cell based therapy. We demonstrated that exosomes isolated from adipose stem cells (ASC) display a neuroprotective role in an in vitro model of ALS. Moreover, the internalization of ASC-exosomes by the cells was shown and the molecules and the mechanisms by which exosomes could exert their beneficial effect were addressed. We performed for the first time a comprehensive proteomic analysis of exosomes derived from murine ASC. We identified a total of 189 proteins and the shotgun proteomics analysis revealed that the exosomal proteins are mainly involved in cell adhesion and negative regulation of the apoptotic process. We correlated the protein content to the anti-apoptotic effect of exosomes observing a downregulation of pro-apoptotic proteins Bax and cleaved caspase-3 and upregulation of anti-apoptotic protein Bcl-2 α, in an in vitro model of ALS after cell treatment with exosomes. Overall, this study shows the neuroprotective effect of ASC-exosomes after their internalization and their global protein profile, that could be useful to understand how exosomes act, demonstrating that they can be employed as therapy in neurodegenerative diseases.


2011 ◽  
Vol 74 (12) ◽  
pp. 2846-2855 ◽  
Author(s):  
Rosa Lippolis ◽  
Antonio Gnoni ◽  
Anna Abbrescia ◽  
Damiano Panelli ◽  
Stefania Maiorano ◽  
...  

Metallomics ◽  
2014 ◽  
Vol 6 (10) ◽  
pp. 1958-1969 ◽  
Author(s):  
John A. Thomas ◽  
Peter Chovanec ◽  
John F. Stolz ◽  
Partha Basu

Insight into the organoarsenic metabolism of Alkaliphilus oremlandii OhILAs by comprehensive proteomic analysis.


2018 ◽  
Vol 12 (3) ◽  
pp. 1870020
Author(s):  
Liming Shen ◽  
Kaoyuan Zhang ◽  
Chengyun Feng ◽  
Youjiao Chen ◽  
Shuiming Li ◽  
...  

PROTEOMICS ◽  
2013 ◽  
Vol 13 (16) ◽  
pp. 2469-2481 ◽  
Author(s):  
Lei Zhou ◽  
Ruihua Wei ◽  
Ping Zhao ◽  
Siew Kwan Koh ◽  
Roger W. Beuerman ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-11
Author(s):  
Chang Yeon Kim ◽  
Jang Ho Ahn ◽  
Do Hyun Han ◽  
Cherl NamKoong ◽  
Hyung Jin Choi

The hypothalamus plays a central role in the integrated regulation of feeding and energy homeostasis. The hypothalamic arcuate nucleus (ARC) contains a population of neurons that express orexigenic and anorexigenic factors and is thought to control feeding behavior via several neuronal circuits. In this study, a comparative proteomic analysis of low-fat control diet- (LFD-) and high-fat diet- (HFD-) induced hypothalamic ARC was performed to identify differentially expressed proteins (DEPs) related to changes in body weight. In the ARC in the hypothalamus, 6621 proteins ( FDR < 0.01 ) were detected, and 178 proteins were categorized as DEPs (89 upregulated and 89 downregulated in the HFD group). Among the Gene Ontology molecular function terms associated with the DEPs, protein binding was the most significant. Fibroblast growth factor receptor substrate 2 (Frs2) and SHC adaptor protein 3 (Shc3) were related to protein binding and involved in the neurotrophin signaling pathway according to Kyoto Encyclopedia of Genes and Genomes analysis. Furthermore, high-precision quantitative proteomic analysis revealed that the protein profile of the ARC in mice with HFD-induced obesity differed from that in LFD mice, thereby offering insight into the molecular basis of feeding regulation and suggesting Frs2 and Shc3 as novel treatment targets for central anorexigenic signal induction.


2011 ◽  
Vol 2011 ◽  
pp. 1-12 ◽  
Author(s):  
Dechassa Duressa ◽  
Khairy Soliman ◽  
Robert Taylor ◽  
Zachary Senwo

Toxic levels of aluminum (Al) in acid soils inhibit root growth and cause substantial reduction in yields of Al-sensitive crops. Aluminum-tolerant cultivars detoxify Al through multiple mechanisms that are currently not well understood at genetic and molecular levels. To enhance our understanding of the molecular mechanisms involved in soybean Al tolerance and toxicity, we conducted proteomic analysis of soybean roots under Al stress using a tandem combination of 2-D-DIGE, mass spectrometry, and bioinformatics tools and Al-tolerant (PI 416937) and Al-sensitive (Young) soybean genotypes at 6, 51 or 72 h of Al treatment. Comparison of the protein profile changes revealed that aluminum induced Al tolerance related proteins and enzymes in Al-tolerant PI 416937 but evoked proteins related to general stress response in Al-sensitive Young. Specifically, Al upregulated: malate dehydrogenase, enolase, malate oxidoreductase, and pyruvate dehydrogenase, in PI 416937 but not in Young. These enzymes contribute to increased synthesis of citrate, a key organic acid involved in Al detoxification. We postulate that simultaneous transgenic overexpression of several of these enzymes would be a robust genetic engineering strategy for developing Al-tolerant crops.


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