The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Placenta-derived exosomes continuously increase in maternal circulation over the first trimester of pregnancy
Open accessAbstract
BACKGROUND: Human placenta releases specific nanovesicles (i.e. exosomes) into the maternal circulation during pregnancy, however, the presence of placenta-derived exosomes in maternal blood during early pregnancy remains to be established. The aim of this study was to characterise gestational age related changes in the concentration of placenta-derived exosomes during the first trimester of pregnancy (i.e. from 6 to 12 weeks) in plasma from women with normal pregnancies. METHODS: A time-series experimental design was used to establish pregnancy-associated changes in maternal plasma exosome concentrations during the first trimester. A series of plasma were collected from normal healthy women (10 patients) at 6, 7, 8, 9, 10, 11 and 12 weeks of gestation (n = 70). We measured the stability of these vesicles by quantifying and observing their protein and miRNA contents after the freeze/thawing processes. Exosomes were isolated by differential and buoyant density centrifugation using a sucrose continuous gradient and characterised by their size distribution and morphology using the nanoparticles tracking analysis (NTA; Nanosight™) and electron microscopy (EM), respectively. The total number of exosomes and placenta-derived exosomes were determined by quantifying the immunoreactive exosomal marker, CD63 and a placenta-specific marker (Placental Alkaline Phosphatase PLAP). RESULTS: These nanoparticles are extraordinarily stable. There is no significant decline in their yield with the freeze/thawing processes or change in their EM morphology. NTA identified the presence of 50-150 nm spherical vesicles in maternal plasma as early as 6 weeks of pregnancy. The number of exosomes in maternal circulation increased significantly (ANOVA, p = 0.002) with the progression of pregnancy (from 6 to 12 weeks). The concentration of placenta-derived exosomes in maternal plasma (i.e. PLAP+) increased progressively with gestational age, from 6 weeks 70.6 ± 5.7 pg/ml to 12 weeks 117.5 ± 13.4 pg/ml. Regression analysis showed that weeks is a factor that explains for >70% of the observed variation in plasma exosomal PLAP concentration while the total exosome number only explains 20%. CONCLUSIONS: During normal healthy pregnancy, the number of exosomes present in the maternal plasma increased significantly with gestational age across the first trimester of pregnancy. This study is a baseline that provides an ideal starting point for developing early detection method for women who subsequently develop pregnancy complications, clinically detected during the second trimester. Early detection of women at risk of pregnancy complications would provide an opportunity to develop and evaluate appropriate intervention strategies to limit acute adverse sequel.
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Cites
1 retracted
RETRACTED: MicroRNA signatures of tumor-derived exosomes as diagnostic biomarkers of ovarian cancer
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RetractedIsolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids
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Exosomes: composition, biogenesis and function
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Classification, Functions, and Clinical Relevance of Extracellular Vesicles
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The majority of microRNAs detectable in serum and saliva is concentrated in exosomes
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Exosomes and Cardiac Repair After Myocardial Infarction
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Human placental trophoblasts confer viral resistance to recipient cells
Delorme-Axford, E., Donker, R. B., Mouillet, J.-F., Chu, T., Bayer, A., Ouyang, Y., Wang, T., Stolz, D. B., Sarkar, S. N., Morelli, A. E., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1304718110 · Cited by 492
Cited by
Burton, G. J., & Jauniaux, E. (2015) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2015.07.050 · Cited by 342
Effects of storage temperature on airway exosome integrity for diagnostic and functional analyses
Maroto, R., Zhao, Y., Jamaluddin, M., Popov, V. L., Wang, H., Kalubowilage, M., Zhang, Y., Luisi, J., Sun, H., Culbertson, C. T., et al. (2017) · Journal of Extracellular Vesicles · doi:10.1080/20013078.2017.1359478 · Cited by 310
Salomon, C., Scholz-Romero, K., Sarker, S., Sweeney, E., Kobayashi, M., Correa, P., Longo, S., Duncombe, G., Mitchell, M. D., Rice, G. E., et al. (2016) · Diabetes · doi:10.2337/db15-0966 · Cited by 299
Self-citationExosomes as drug carriers for cancer therapy and challenges regarding exosome uptake
Zhao, X., Wu, D., Ma, X., Wang, J., Hou, W., & Zhang, W. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110237 · Cited by 197
Extracellular Vesicles in Blood: Sources, Effects, and Applications
Alberro, A., Iparraguirre, L., Fernandes, A., & Otaegui, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158163 · Cited by 170
Metadata
- Authors
- Sarker, S., Scholz-Romero, K., Perez, A., Illanes, S. E., Mitchell, M. D., Rice, G. E., & Salomon, C.
- Venue
- Journal of Translational Medicine
- Published
- 2014-08-08
- Volume
- 12
- Issue
- 1
- Pages
- 204-204
- ISSN
- 1479-5876 (ISSN-L)
- OpenAlex
- W2151641359
- Cited by
- 411
- References
- 42
- FWCI
- 7.91
- Type
- journal article
- Language
- en
- Open access
- gold
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