2008
DOI: 10.1002/pros.20860
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Structural heterogeneity and protein composition of exosome‐like vesicles (prostasomes) in human semen

Abstract: From the data reported herein, we hypothesize that the structural heterogeneity of the exosome-like particles in human semen reflects their functional diversity. Our detailed proteomic analysis provided a list of candidate proteins for future structural and functional studies.

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Cited by 275 publications
(257 citation statements)
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“…Prostasomes contain many different proteins (15,16). Proteins present on the surface of prostasomes include aminopeptidase N (CD13) (17,18) and tissue factor (CD142), a cell membraneassociated glycoprotein that serves as a receptor and essential cofactor for factors VII and VIIa of the coagulation cascade (19).…”
mentioning
confidence: 99%
“…Prostasomes contain many different proteins (15,16). Proteins present on the surface of prostasomes include aminopeptidase N (CD13) (17,18) and tissue factor (CD142), a cell membraneassociated glycoprotein that serves as a receptor and essential cofactor for factors VII and VIIa of the coagulation cascade (19).…”
mentioning
confidence: 99%
“…Prostasomes molecular composition could reflect their capacity to influence PCa growth and metastasis. Proteomic profile of prostasome isolated from SF identify prostatespecific membrane proteins (like TMPRSS2), prostatespecific transglutaminase, and prostate stem cell antigen (PSCA), confirmed the prostatic origin of these vesicles (16,37,38). The first efforts to identify the prostasomes in a PCa patient's blood was the detection of anti-prostasome antibodies (39)(40)(41).…”
Section: Role Of Prostasomes In Pcamentioning
confidence: 83%
“…On the other hand, exosomes originate from the inward budding of early and late endosomes hence forming MVBs containing ILVs [21,22]. Subsequently, the MVBs are transported to and fuse with the plasma membrane, requiring a dynamic interplay between members of the Rab and SNARE protein family, concurrently releasing the ILVs in the extracellular space [23][24][25][26][27]. Partly because both biogenesis pathway are analogous, to date there is no defined panel of markers to distinguish between both vesicle subtypes in a vesicular isolate.…”
Section: Biogenesis Cargo Loading and Compositionmentioning
confidence: 99%
“…EVs have been isolated from e.g. urine [11], plasma [26], semen [25], nasal secretion [24], breast milk [221], the aqueous humor of eyes [222], cerebrospinal fluid [223], peritoneal fluid [224], bronchoalveolar lavage [225]. Depending on the respective disease for which the biomarker is being developed, an accessible biofluid should be considered in which the EVs of interest are likely the most concentrated and a liquid biopsy can be easily obtained.…”
Section: 2evs As Biomarkermentioning
confidence: 99%