Human autonomic neuronal cell models are emerging as tools for modelling diseases such as cardiac arrhythmias. In this systematic review, we compared thirty-three articles applying fourteen different protocols to generate sympathetic neurons and three different procedures to produce parasympathetic neurons. All methods involved the differentiation of human pluripotent stem cells, and none employed permanent or reversible cell immortalization.
View Article and Find Full Text PDFAlthough variation in effect sizes and predicted values among studies of similar phenomena is inevitable, such variation far exceeds what might be produced by sampling error alone. One possible explanation for variation among results is differences among researchers in the decisions they make regarding statistical analyses. A growing array of studies has explored this analytical variability in different fields and has found substantial variability among results despite analysts having the same data and research question.
View Article and Find Full Text PDFMajor histocompatibility complex class II (MHC-II) presents antigens to T helper cells. The spectrum of presented peptides is regulated by the exchange catalyst human leukocyte antigen DM (HLA-DM), which dissociates peptide-MHC-II complexes in the endosome. How susceptible a peptide is to HLA-DM is mechanistically not understood.
View Article and Find Full Text PDFGunung Palung National Park (GPNP) and the surrounding region in West Kalimantan, Indonesia, host a significant population of Critically Endangered Bornean orangutans (Pongo pygmaeus wurmbii) amidst various conservation challenges, including habitat destruction, the illegal pet trade, and human-wildlife conflict. The Gunung Palung Orangutan Conservation Program (GPOCP) employs diverse strategies, including environmental education, to address these challenges. Environmental education helps to connect local students with conservation efforts, educate them about endangered endemic species, and highlight the relationship between human behavior and ecosystem health.
View Article and Find Full Text PDFFacioscapulohumeral muscular dystrophy (FSHD) is caused by sporadic misexpression of the transcription factor double homeobox 4 (DUX4) in skeletal muscles. So far, monolayer cultures and animal models have been used to study the FSHD disease mechanism and for FSHD therapy development, but these models do not fully recapitulate the disease and there is a lack of knowledge on how DUX4 misexpression leads to skeletal muscle dysfunction. To overcome these barriers, we have developed a three-dimensional tissue engineered skeletal muscle (3D-TESM) model by generating genetically matched myogenic progenitors (MPs) from human induced pluripotent stem cells of three mosaic FSHD patients.
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