Real-time measurements of membrane surface dynamics on macrophages and the phagocytosis of Leishmania parasites

Defocusing microscopy was used for real-time observation and quantification of membrane surface dynamics in murine bone marrow macrophages. Small random membrane fluctuations (SRMF), possibly metabolic driven, were detected uniformly over all membrane surface. Morphological and dynamical parameters...

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Published inExperimental cell research Vol. 303; no. 2; pp. 207 - 217
Main Authors Neto, José Coelho, Agero, Ubirajara, Oliveira, Diogo C.P., Gazzinelli, Ricardo T., Mesquita, Oscar N.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.02.2005
Elsevier BV
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Abstract Defocusing microscopy was used for real-time observation and quantification of membrane surface dynamics in murine bone marrow macrophages. Small random membrane fluctuations (SRMF), possibly metabolic driven, were detected uniformly over all membrane surface. Morphological and dynamical parameters of ruffles, such as shape, dimensions, and velocity of propagation, were analyzed. Optical tweezers were used to promote phagocytosis of single Leishmania amazonensis amastigotes by selected macrophages. Analysis of ruffling activity on the macrophages before and during phagocytosis of the parasites indicated that increased ruffling response near forming phagosomes, most likely induced by the parasite, accelerates phagocytosis. The effects of temperature decrease on the dynamics of membrane surface fluctuations and on the phagocytosis of parasites were used to determine the overall activation energies involved in these processes. The values obtained support the existence of strong correlation between membrane motility and phagocytic capacity.
AbstractList Defocusing microscopy was used for real-time observation and quantification of membrane surface dynamics in murine bone marrow macrophages. Small random membrane fluctuations (SRMF), possibly metabolic driven, were detected uniformly over all membrane surface. Morphological and dynamical parameters of ruffles, such as shape, dimensions, and velocity of propagation, were analyzed. Optical tweezers were used to promote phagocytosis of single Leishmania amazonensis amastigotes by selected macrophages. Analysis of ruffling activity on the macrophages before and during phagocytosis of the parasites indicated that increased ruffling response near forming phagosomes, most likely induced by the parasite, accelerates phagocytosis. The effects of temperature decrease on the dynamics of membrane surface fluctuations and on the phagocytosis of parasites were used to determine the overall activation energies involved in these processes. The values obtained support the existence of strong correlation between membrane motility and phagocytic capacity.
Defocusing microscopy was used for real-time observation and quantification of membrane surface dynamics in murine bone marrow macrophages. Small random membrane fluctuations (SRMF), possibly metabolic driven, were detected uniformly over all membrane surface. Morphological and dynamical parameters of ruffles, such as shape, dimensions, and velocity of propagation, were analyzed. Optical tweezers were used to promote phagocytosis of single Leishmania amazonensis amastigotes by selected macrophages. Analysis of ruffling activity on the macrophages before and during phagocytosis of the parasites indicated that increased ruffling response near forming phagosomes, most likely induced by the parasite, accelerates phagocytosis. The effects of temperature decrease on the dynamics of membrane surface fluctuations and on the phagocytosis of parasites were used to determine the overall activation energies involved in these processes. The values obtained support the existence of strong correlation between membrane motility and phagocytic capacity.
Defocusing microscopy was used for real-time observation and quantification of membrane surface dynamics in murine bone marrow macrophages. Small random membrane fluctuations (SRMF), possibly metabolic driven, were detected uniformly over all membrane surface. Morphological and dynamical parameters of ruffles, such as shape, dimensions, and velocity of propagation, were analyzed. Optical tweezers were used to promote phagocytosis of single Leishmania amazonensis amastigotes by selected macrophages. Analysis of ruffling activity on the macrophages before and during phagocytosis of the parasites indicated that increased ruffling response near forming phagosomes, most likely induced by the parasite, accelerates phagocytosis. The effects of temperature decrease on the dynamics of membrane surface fluctuations and on the phagocytosis of parasites were used to determine the overall activation energies involved in these processes. The values obtained support the existence of strong correlation between membrane motility and phagocytic capacity. [PUBLICATION ABSTRACT]
Author Neto, José Coelho
Agero, Ubirajara
Gazzinelli, Ricardo T.
Mesquita, Oscar N.
Oliveira, Diogo C.P.
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  givenname: Oscar N.
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Issue 2
Keywords Membrane ruffles
Membrane fluctuations
Membrane motility
Defocusing microscopy
Phagocytosis
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Snippet Defocusing microscopy was used for real-time observation and quantification of membrane surface dynamics in murine bone marrow macrophages. Small random...
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StartPage 207
SubjectTerms Animals
Bone Marrow Cells - parasitology
Bone Marrow Cells - physiology
Cell Membrane - physiology
Defocusing microscopy
In Vitro Techniques
Leishmania mexicana - pathogenicity
Macrophages - parasitology
Macrophages - physiology
Membrane fluctuations
Membrane motility
Membrane ruffles
Mice
Mice, Inbred C57BL
Microscopy, Video - methods
Movement
Phagocytosis
Phagocytosis - physiology
Thermodynamics
Title Real-time measurements of membrane surface dynamics on macrophages and the phagocytosis of Leishmania parasites
URI https://dx.doi.org/10.1016/j.yexcr.2004.09.002
https://www.ncbi.nlm.nih.gov/pubmed/15652336
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https://search.proquest.com/docview/67372011
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