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Eeva-Liisa Eskelinen

Researcher at University of Turku

Publications -  136
Citations -  32990

Eeva-Liisa Eskelinen is an academic researcher from University of Turku. The author has contributed to research in topics: Autophagy & Endosome. The author has an hindex of 60, co-authored 124 publications receiving 28293 citations. Previous affiliations of Eeva-Liisa Eskelinen include Dalhousie University & University of Kiel.

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Journal ArticleDOI

Piecemeal microautophagy of the nucleus: Genetic and morphological traits

TL;DR: The morphological analysis of PMN is extended using immunogold and freeze fracture electron microscopy to investigate the functions of the highly conserved but poorly understood core autophagic apparatus.
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Tracing uptake of C3dg-conjugated antigen into B cells via complement receptor type 2 (CR2, CD21)

TL;DR: These data provide the first ultrastructural evidence that complement-coated antigens are endocytosed by antigen-nonspecific B cells by CR2 and are delivered to the compartments in which peptide loading for antigen presentation occurs and support the notion that CR2 may play a role in antigen presentation by B cells regardless of B-cell receptor specificity.
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Quantitative proteomics of extracellular vesicles released from human monocyte-derived macrophages upon β-glucan stimulation

TL;DR: High-throughput quantitative proteomics combined with bioinformatics and detailed pathway and network analysis showed that integrins and their cytoplasmic cargo proteins are highly abundant in extracellular vesicles released upon β-glucan stimulation, providing a solid basis for further studies on the functional role of vesicular protein secretion upon fungal infection.
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Calpain as a novel regulator of autophagosome formation.

TL;DR: It is found that autophagy is impaired in Capns1-deficient cells by immunostaining of the endogenous autophagosome marker LC3 and electron microscopy experiments, and the enhancement of lysosomal activity and long-lived proteins degradation, normally occurring upon starvation, are also reduced.