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FIGURE 4 Atomic force microscopy <t>(AFM)-based</t> morphometry and nanomechanical screening. (A) Representative AFM <t>micrographs</t> of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.
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FIGURE 4 Atomic force microscopy <t>(AFM)-based</t> morphometry and nanomechanical screening. (A) Representative AFM <t>micrographs</t> of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.
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FIGURE 4 Atomic force microscopy <t>(AFM)-based</t> morphometry and nanomechanical screening. (A) Representative AFM <t>micrographs</t> of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.
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FIGURE 4 Atomic force microscopy <t>(AFM)-based</t> morphometry and nanomechanical screening. (A) Representative AFM <t>micrographs</t> of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.
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FIGURE 4 Atomic force microscopy <t>(AFM)-based</t> morphometry and nanomechanical screening. (A) Representative AFM <t>micrographs</t> of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.
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FIGURE 4 Atomic force microscopy <t>(AFM)-based</t> morphometry and nanomechanical screening. (A) Representative AFM <t>micrographs</t> of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.
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FIGURE 4 Atomic force microscopy (AFM)-based morphometry and nanomechanical screening. (A) Representative AFM micrographs of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.

Journal: The FASEB Journal

Article Title: Platelets as key cells in endometriosis patients: Insights from small extracellular vesicles in peritoneal fluid and endometriotic lesions analysis

doi: 10.1096/fj.202402499r

Figure Lengend Snippet: FIGURE 4 Atomic force microscopy (AFM)-based morphometry and nanomechanical screening. (A) Representative AFM micrographs of the three sample types. (B) Contact angle (CA) vs diameter plot of individual particles measured from at least 10 AFM micrographs deposited from duplicate preparations (Endo: N = 227; Con: N = 296; FF: N = 3632). The contact angle can be regarded as a measure of the mechanical stiffness of EVs; all particles above ~45 nm display the typical conserved average CA of intact vesicles, whereas smaller particles do not. (C) Normalized relative surface density of particles with diameters greater than 45 nm, showing that the FF samples are consistently more concentrated than the Endo and Con samples. (D) Box plot of the measured diameters of individual vesicles greater than 45 nm shows how FF samples contained the most significant proportion of larger EVs, while Endo samples contained the smallest. Con, control sample; Endo, endometriosis sample; FF, follicular fluid sample.

Article Snippet: AFM micrographs were recorded in liquid at RT on a Multimode 8 microscope (Bruker, USA) equipped with Scanasyst Fluid+ probes (Bruker, USA) and operated in peak force mode.

Techniques: Microscopy, Control