studying-organelle-dynamics-in-b-cells-during-immune-synapse-formation

Studying Organelle Dynamics in B Cells During Immune Synapse Formation

Recognition of surface-tethered antigens&#160;by the B cell receptor (BCR)&#160;triggers the formation of an immune synapse (IS), where both ...

Pontificia Universidad Católica de Chile

Megalin is a large endocytic receptor with relevant functions during development and adult life. It is expressed at the apical surface of several epithelial cell types, including proximal tubule cells (PTCs) in the kidney, where it internalizes apolipoproteins, vitamins and hormones with their corresponding carrier proteins and signaling molecules. Despite the important physiological roles of megalin little is known about the regulation of its expression. By analyzing the human megalin promoter, we found three response elements for the peroxisomal proliferator-activated receptor (PPAR). The objective of this study was to test whether megalin expression is regulated by the PPARs.

Megalin/LRP2 expression is induced by peroxisome proliferator-activated receptor -alpha and -gamma: implications for PPARs' roles in renal function.

Lysosomes are dynamic organelles, which can fuse with a variety of targets and undergo constant regeneration. They can move along microtubules in a retrograde and anterograde fashion by using motor proteins, kinesin and dynein, being main players in extracellular secretion, intracellular components degradation and recycling. Moreover, lysosomes interact with other intracellular organelles to regulate their turnover, such as ER, mitochondria and peroxisomes. The correct localization of lysosomes is relevant in several physiological processes, including appropriate antigen presentation, neurotransmission and receptors modulation in neuronal synapsis, whereas hepatic lysosomes and autophagy are master regulators of nutrient homeostasis. Alterations in lysosome function due to mutation of genes encoding lysosomal proteins, soluble hydrolases as well as membrane proteins, lead to lysosomal storage diseases (LSDs). Lysosomes containing undegraded substrates are finally stacked and therefore miss positioned inside the cell, leading to lysosomal dysfunction, which impacts a wide range of cellular functions.

Jonathan Lagos

Laboratory of Immune Cell Biology,
Department of Cellular and Molecular Biology,
Faculty of Medicine,
Laboratory of Immune Cell Biology, Department of Cellular and Molecular Biology

Pontificia Universidad Católica de Chile

Studying Organelle Dynamics in B Cells During Immune Synapse Formation

Jonathan Lagos

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Laboratory of Immune Cell Biology,Department of Cellular and Molecular Biology,Faculty of Medicine,Laboratory of Immune Cell Biology, Department of Cellular and Molecular Biology

Pontificia Universidad Católica de Chile

Studying Organelle Dynamics in B Cells During Immune Synapse Formation

Laboratory of Immune Cell Biology,
Department of Cellular and Molecular Biology,
Faculty of Medicine,
Laboratory of Immune Cell Biology, Department of Cellular and Molecular Biology