Zobrazeno 1 - 10
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pro vyhledávání: '"Phagocytic cup"'
Phagocytosis is the mechanism of the internalization of large particles, microorganisms and cellular debris. The complement pathway represents one of the first mechanisms of defense against infection and the complement receptor 3 (CR3), which is high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f09297882ae1b6b4aa75c161a7f24d3
https://hal.archives-ouvertes.fr/hal-03453678
https://hal.archives-ouvertes.fr/hal-03453678
Autor:
Sarah R. Barger, Nils C. Gauthier, Mira Krendel, Daan Vorselen, Julie A. Theriot, Wei Cai, Yifan Wang
Publikováno v:
eLife
eLife, Vol 10 (2021)
eLife, Vol 10 (2021)
Phagocytosis requires rapid actin reorganization and spatially controlled force generation to ingest targets ranging from pathogens to apoptotic cells. How actomyosin activity directs membrane extensions to engulf such diverse targets remains unclear
Autor:
Je-Yoel Cho, Seung Yoon Park, Jae Hoon Pyo, Soyoun Kim, In San Kim, Jae Do Yoo, Sang Yeob Kim, Dong Jun Bae, Junyoung Seo, Wonhwa Cho
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1866:1595-1607
The rapid and precise clearance of apoptotic cells (efferocytosis) involves a series of phagocytic processes through which apoptotic cells are recognized, engulfed, and degraded within phagocytes. The Rho-family GTPases critically rearrange the cytos
Publikováno v:
Nature cell biology
αMβ2 integrin (complement receptor 3) is a major receptor for phagocytosis in macrophages. In other contexts, integrins' activities and functions are mechanically linked to actin dynamics through focal adhesions. We asked whether mechanical couplin
Publikováno v:
Biochemical and Biophysical Research Communications. 515:163-168
It has been proposed that Ca2+ activation of calpain-1 is important for the rapid cell shape changes which accompany phagocytosis. In this paper, we use a fluorogenic calpain substrate, (CBZ-Ala Ala)2 R110, and find that there was a low calpain activ
Membrane-cytoskeletal crosstalk mediated by myosin-I regulates adhesion turnover during phagocytosis
Autor:
John M. Heddleston, Qingsen Li, Nils C. Gauthier, Richard A. Flavell, Nicholas S. Reilly, Tatyana Svitkina, Mark S. Mooseker, Maria S. Shutova, Paolo Maiuri, Sarah R. Barger, Patrick W. Oakes, Mira Krendel
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-18 (2019)
Nature Communications
Nature Communications
Phagocytosis of invading pathogens or cellular debris requires a dramatic change in cell shape driven by actin polymerization. For antibody-covered targets, phagocytosis is thought to proceed through the sequential engagement of Fc-receptors on the p
Autor:
Xuehua Xu, Keqiang Chen, Xi Wen, Tian Jin, Ji Ming Wang, Miao Pan, Silvia Bolland, Wenxiang Sun
Publikováno v:
Molecular Biology of the Cell
A dogma of innate immunity is that neutrophils use G-protein–coupled receptors (GPCRs) for chemoattractant to chase bacteria through chemotaxis and then use phagocytic receptors coupled with tyrosine kinases to destroy opsonized bacteria via phagoc
Autor:
Hans C. Leier, Fabian Pott, Caroline Barisch, Patrick Niekamp, Fikadu G. Tafesse, Ali Rashidfarrokhi, Veronica Richina, Gaelen Guzman, Joost C. M. Holthuis
Publikováno v:
mBio
mBio, Vol 12, Iss 1 (2021)
mBio, Vol 12, Iss 1 (2021)
Mycobacterium tuberculosis (Mtb) invades alveolar macrophages through phagocytosis to establish infection and cause disease. The molecular mechanisms underlying Mtb entry are still poorly understood.
Phagocytosis by alveolar macrophages is the o
Phagocytosis by alveolar macrophages is the o
Autor:
Markus Horsthemke, Peter J. Hanley, Anne C. Bachg, Stefan Walbaum, Attila Mócsai, Benjamin Ambrosy, Jeanette H. W. Leusen, Paula Schütz
Publikováno v:
The Journal of Biological Chemistry
A long-standing hypothesis is that complement receptors (CRs), especially CR3, mediate sinking phagocytosis, but evidence is lacking. Alternatively, CRs have been reported to induce membrane ruffles or phagocytic cups, akin to those induced by Fcγ r
Autor:
Wen-Biao Gan, Zongyue Cheng, Laetitia Weinhard, Alexia Tiberi, Ruohe Zhao, Alejandro Martin-Avila
Publikováno v:
Alzheimer's & Dementia. 16