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Proteomic analysis of human placental syncytiotrophoblast microvesicles in preeclampsia

BACKGROUND: Placental syncytiotrophoblast microvesicles (STBM) are shed into the maternal circulation during normal pregnancy. STBM circulate in significantly increased amounts in preeclampsia (PE) and are considered to be among contributors to the exaggerated proinflammatory, procoagulant state of...

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Detalles Bibliográficos
Autores principales: Baig, Sonia, Kothandaraman, Narasimhan, Manikandan, Jayapal, Rong, Li, EE, Kim Huey, Hill, Jeffrey, Lai, Chin Wee, Tan, Wan Yu, Yeoh, Felicia, Kale, Anita, Su, Lin Lin, Biswas, Arijit, Vasoo, Sheila, Choolani, Mahesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247627/
https://www.ncbi.nlm.nih.gov/pubmed/25469110
http://dx.doi.org/10.1186/1559-0275-11-40
Descripción
Sumario:BACKGROUND: Placental syncytiotrophoblast microvesicles (STBM) are shed into the maternal circulation during normal pregnancy. STBM circulate in significantly increased amounts in preeclampsia (PE) and are considered to be among contributors to the exaggerated proinflammatory, procoagulant state of PE. However, protein composition of STBM in normal pregnancy and PE remains unknown. We therefore sought to determine the protein components of STBM and whether STBM protein expressions differ in preeclamptic and normal pregnancies. Patients with PE (n = 3) and normal pregnant controls (n = 6) were recruited. STBM were prepared from placental explant culture supernatant. STBM proteins were analyzed by a combination of 1D Gel-LC-MS/MS. Protein expressions levels were quantified using spectral counts and validated by immunohistochemistry. RESULTS: Over 400 proteins were identified in the STBM samples. Among these, 25 proteins were found to be differentially expressed in preeclampsia compared to healthy pregnant controls, including integrins, annexins and histones. CONCLUSION: STBM proteins include those that are implicated in immune response, coagulation, oxidative stress, apoptosis as well as lipid metabolism pathways. Differential protein expressions of STBM suggest their pathophysiological relevance in PE. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1559-0275-11-40) contains supplementary material, which is available to authorized users.