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 in | Experimental cell research Vol. 303; no. 2; pp. 207 - 217 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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15.02.2005
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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. |
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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. |
Author_xml | – sequence: 1 givenname: José Coelho surname: Neto fullname: Neto, José Coelho email: rabbit@fisica.ufmg.br organization: Departamento de Física, ICEx, Universidade Federal de Minas Gerais, CEP 30123-970, Belo Horizonte, Minas Gerais, Brasil – sequence: 2 givenname: Ubirajara surname: Agero fullname: Agero, Ubirajara organization: Departamento de Física, ICEx, Universidade Federal de Minas Gerais, CEP 30123-970, Belo Horizonte, Minas Gerais, Brasil – sequence: 3 givenname: Diogo C.P. surname: Oliveira fullname: Oliveira, Diogo C.P. organization: Centro de Pesquisas René Rachou, FIOCRUZ, CEP 30190-002, Belo Horizonte, Minas Gerais, Brasil – sequence: 4 givenname: Ricardo T. surname: Gazzinelli fullname: Gazzinelli, Ricardo T. organization: Departamento de Bioquímica e Imunologia, ICB, Universidade Federal de Minas, Gerais, CEP 30123-970, Belo Horizonte, Minas Gerais, Brasil – sequence: 5 givenname: Oscar N. surname: Mesquita fullname: Mesquita, Oscar N. organization: Departamento de Física, ICEx, Universidade Federal de Minas Gerais, CEP 30123-970, Belo Horizonte, Minas Gerais, Brasil |
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CitedBy_id | crossref_primary_10_1103_PhysRevLett_98_168103 crossref_primary_10_1103_PhysRevE_74_041903 crossref_primary_10_1063_1_3136842 crossref_primary_10_1590_S0001_37652007000100003 crossref_primary_10_1016_j_biosystems_2012_06_001 crossref_primary_10_1088_1742_5468_2006_11_P11007 crossref_primary_10_1103_PhysRevE_78_041911 crossref_primary_10_1529_biophysj_105_062224 crossref_primary_10_1186_1471_2180_13_107 crossref_primary_10_1063_1_4884420 crossref_primary_10_1063_1_2189010 crossref_primary_10_4049_jimmunol_175_5_3214 crossref_primary_10_1098_rsta_2007_2091 crossref_primary_10_1371_journal_pone_0097855 crossref_primary_10_1209_0295_5075_84_58008 crossref_primary_10_1016_j_bpj_2013_07_036 crossref_primary_10_1088_1361_6633_aa8730 crossref_primary_10_1529_biophysj_105_073783 |
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Keywords | Membrane ruffles Membrane fluctuations Membrane motility Defocusing microscopy Phagocytosis |
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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 |
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