scholarly journals Genetic compensation between Pax3 and Pax7 in zebrafish appendicular muscle formation

2021 ◽  
Author(s):  
Hanna Nord ◽  
Abraha Kahsay ◽  
Nils Dennhag ◽  
Fatima Pedrosa Domellöf ◽  
Jonas von Hofsten
Author(s):  
Christine E Wamsley ◽  
Mikaela Kislevitz ◽  
Jennifer Barillas ◽  
Deniz Basci ◽  
Vishal Kandagatla ◽  
...  

Abstract Background While ablative techniques have been standard of care for the treatment of fine lines and wrinkles, microneedling is a minimally invasive alternative. Objectives The purpose of this study was to assess the efficacy of microneedling on facial and neck fine lines and wrinkles. Methods 35 subjects between 44 and 65 years old with Fitzpatrick skin types I-IV received four monthly microneedling treatments over the face and neck. Subjects returned one and three months post-treatment. At every visit, high-resolution ultrasonography, optical coherence tomography, transepidermal water loss and BTC-2000 were performed. 0.33mm microbiopsies were collected pre-treatment, before the fourth treatment and three months post-treatment. Results 32 subjects (93.75% female, 6.25% male) completed all seven visits. Facial dermal and epidermal density increased 101.86% and 19.28%, respectively from baseline at three months post-treatment. Facial elasticity increased 28.2% from baseline three months post-treatment. Facial attenuation coefficient increased 15.65% and 17.33% one and three months post-treatment. At study completion, blood flow 300µm deep decreased 25.8% in the face and 42.3% in the neck. Relative collagen type III and elastin gene expression was statistically higher three months post-treatment. However, total elastin protein levels unchanged compared to baseline. 58% of biopsies extracted three months post-treatment showed dermal muscle formation, compared to baseline 15.3%. Conclusions The results illustrate the effects of microneedling treatments. Non-invasive measurements and biopsy data showed changes in skin architecture and collagen/elastin gene expression suggesting skin rejuvenation, with new extracellular matrix production and muscle formation.


Nature ◽  
2019 ◽  
Vol 568 (7751) ◽  
pp. 193-197 ◽  
Author(s):  
Mohamed A. El-Brolosy ◽  
Zacharias Kontarakis ◽  
Andrea Rossi ◽  
Carsten Kuenne ◽  
Stefan Günther ◽  
...  

Cell ◽  
2018 ◽  
Vol 175 (3) ◽  
pp. 877-886.e10 ◽  
Author(s):  
Patrick Harrigan ◽  
Hiten D. Madhani ◽  
Hana El-Samad

2018 ◽  
Vol 9 ◽  
Author(s):  
José Antonio González-Gutiérrez ◽  
Diana Fabiola Díaz-Jiménez ◽  
Itzel Vargas-Pérez ◽  
Gabriel Guillén-Solís ◽  
Jörg Stülke ◽  
...  

2021 ◽  
Vol 134 (14) ◽  

ABSTRACT First Person is a series of interviews with the first authors of a selection of papers published in Journal of Cell Science, helping early-career researchers promote themselves alongside their papers. Magdalena Cardenas-Rodriguez is first author on ‘ Genetic compensation for cilia defects in cep290 mutants by upregulation of cilia-associated small GTPases’, published in JCS. Magdalena is a research assistant in the lab of Jose Luis Badano at Human Molecular Genetics Laboratory, Institut Pasteur de Montevideo, Montevideo, Uruguay, investigating the cellular processes that are altered in cilia-related human diseases.


eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Daniel Sieiro ◽  
Anne C Rios ◽  
Claire E Hirst ◽  
Christophe Marcelle

How cells in the embryo coordinate epithelial plasticity with cell fate decision in a fast changing cellular environment is largely unknown. In chick embryos, skeletal muscle formation is initiated by migrating Delta1-expressing neural crest cells that trigger NOTCH signaling and myogenesis in selected epithelial somite progenitor cells, which rapidly translocate into the nascent muscle to differentiate. Here, we uncovered at the heart of this response a signaling module encompassing NOTCH, GSK-3β, SNAI1 and β-catenin. Independent of its transcriptional function, NOTCH profoundly inhibits GSK-3β activity. As a result SNAI1 is stabilized, triggering an epithelial to mesenchymal transition. This allows the recruitment of β-catenin from the membrane, which acts as a transcriptional co-factor to activate myogenesis, independently of WNT ligand. Our results intimately associate the initiation of myogenesis to a change in cell adhesion and may reveal a general principle for coupling cell fate changes to EMT in many developmental and pathological processes.


Author(s):  
Marisol León ◽  
A. C. B. Rodrigues ◽  
A. O. M. Turquetti ◽  
A. D. Cereta ◽  
L. F. Melo ◽  
...  

Aims: We propose to briefly review the specific role of lipids in embryonic structures development. Results: Lipids are organic substances insoluble in water, divided into several classes, such as fatty acids, glycolipids, phospholipids, ceramides, sphingolipids, and stereo-lipids. They participate in processes of cellular metabolism and embryonic development which are associated with signalling, proliferation and cell migration. They act in developmental processes such as calcification and bone mineralization, pulmonary maturity, cellular differentiation, and neural survival, epithelial cells polarization and muscle formation, in which phospholipids as a major group, work more regularly. Lipids during embryonic development work directly as transport molecules or cell markers. In addition to an imbalance in its enzymatic and protein precursors (such as choline kinase), lipids can increase or decrease lipid concentration in cells, prevent its biotransformation, or affect its synergy with other molecules, leading to failures in the formation of organs such as the heart, brain, and bones. This aims to further the understanding of these processes and highlight its feasibility for future clinical applications. Conclusion: Lipids maintain cell membrane integrity in blastocysts, transport calcium to nerve and bone cells, facilitate neural apoptosis, and promote pulmonary maturation. These results aid in the understanding and prediction of alterations in lipidic metabolic syndromes in several pathological disorders during organ development.


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