
Thomas Neufeld
· ProfessorUniversity of Minnesota · Cell Biology
Active 1991–2023
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About
Thomas Neufeld, PhD, is a professor affiliated with the Genetics, Cell Biology & Development department at the University of Minnesota Medical School. His professional profile is accessible through the university's website, indicating his role within the academic community. The information provided does not specify his research focus, background, or key contributions, but it confirms his position as a faculty member involved in genetics, cell biology, and development.
Research topics
- Medicine
- Genetics
- Biology
- Art
- Pediatrics
- Cell biology
- Internal medicine
- Philosophy
- Gerontology
- Theology
Selected publications
ULK1 induces autophagy by phosphorylating Beclin-1 and activating VPS34 lipid kinase
Nature Cell Biology · 2013-05-19 · 1529 citations
articleOpen accessAutophagy · 2015-07-09 · 789 citations
articleOpen accessSenior authorCorrespondingAutophagosome-lysosome fusion and autolysosome acidification constitute late steps in the autophagic process necessary to maintain functional autophagic flux and cellular homeostasis. Both of these steps are disrupted by the V-ATPase inhibitor bafilomycin A1, but the mechanisms potentially linking them are unclear. We recently revisited the role of lysosomal acidification in autophagosome-lysosome fusion, using an in vivo approach in Drosophila. By genetically depleting individual subunits of th…
Autophagosome–lysosome fusion is independent of V-ATPase-mediated acidification
Nature Communications · 2015-05-11 · 432 citations
articleOpen accessSenior authorThe ATP-dependent proton pump V-ATPase ensures low intralysosomal pH, which is essential for lysosomal hydrolase activity. Based on studies with the V-ATPase inhibitor BafilomycinA1, lysosomal acidification is also thought to be required for fusion with incoming vesicles from the autophagic and endocytic pathways. Here we show that loss of V-ATPase subunits in the Drosophila fat body causes an accumulation of non-functional lysosomes, leading to a block in autophagic flux. However, V-ATPase-defi…
Nature Communications · 2015-04-17 · 187 citations
articleOpen accessSenior authorSecreted ligands of the insulin family promote cell growth and maintain sugar homeostasis. Insulin release is tightly regulated in response to dietary conditions, but how insulin-producing cells (IPCs) coordinate their responses to distinct nutrient signals is unclear. Here we show that regulation of insulin secretion in Drosophila larvae has been segregated into distinct branches—whereas amino acids promote the secretion of Drosophila insulin-like peptide 2 (Dilp2), circulating sugars promote t…
Membrane remodeling by the PX-BAR protein SNX18 promotes autophagosome formation
The Journal of Cell Biology · 2013-07-22 · 178 citations
articleOpen accessThe membrane remodeling events required for autophagosome biogenesis are still poorly understood. Because PX domain proteins mediate membrane remodeling and trafficking, we conducted an imaging-based siRNA screen for autophagosome formation targeting human PX proteins. The PX-BAR protein SNX18 was identified as a positive regulator of autophagosome formation, and its Drosophila melanogaster homologue SH3PX1 was found to be required for efficient autophagosome formation in the larval fat body. We…
Recent grants
NIH · $3.8M · 2015
Frequent coauthors
- 21 shared
Elaine C.M. Silva-Zacarin
- 20 shared
Anna Nogalska
Broad Center
- 20 shared
Wen H. Yu
Wuhan University of Technology
- 19 shared
Dieter Willbold
Heinrich Heine University Düsseldorf
- 19 shared
Gerald M. Rubin
Howard Hughes Medical Institute
- 18 shared
Xuejun Jiang
- 17 shared
Frank C. Dorsey
- 16 shared
Frank Lafont
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