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Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia.

Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Research Abstract Details 

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  • Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Abstract Text:

    jennifer k ho-chenJennifer K Ho-Chen,juan j bustamanteJuan J Bustamante,michael j soaresMichael J Soares,

    The prolactin (PRL) family of hormones/cytokines is involved in the maintenance of pregnancy and adaptations to physiological stressors. In this report, we identify and characterize a new member of the rat PRL family, examine the impact of maternal hypoxia on placental PRL family gene expression, and investigate maternal adaptive responses to hypoxia. Perusal of the PRL gene family locus in the rat genome resulted in the identification of a putative new member of the rat PRL family. The new member is closely related to the previously reported PRL-like protein-F (PLP-F) and has been named PLP-Fbeta and the originally characterized PLP-F, now termed PLP-Falpha. The two proteins exhibit structural similarities but possess distinct cell- and temporal-specific expression profiles. In vivo hypoxia stimulates placental PLP-Falpha and PLP-E mRNA expression in the rat and mouse, respectively. Rcho-1 trophoblast cells can differentiate into trophoblast giant cells, express PLP-Falpha, and exhibit enhanced PLP-Falpha mRNA levels when cultured under low oxygen tension (2%). Exposure to hypobaric hypoxia during latter part of pregnancy did not significantly impact the expression of PLP-Fbeta mRNA. Finally, exposure to hypobaric hypoxia during midpregnancy led to increased maternal red blood cells, hemoglobin concentrations, hematocrit, and increased concentrations of maternal splenic mRNAs for key proteins involved in hemoglobin synthesis, erythroid Krüppel-like factor, erythroid 5-aminolevulinate synthase-2, and beta-major globin. In summary, adaptive responses to maternal hypoxia include activation of placental PLP-Falpha/E gene expression, which may then participate in maternal hematological adjustments required for maintaining maternal and fetal oxygen delivery.

    Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Publishing Authors By Initials

    jk ho-chenJK Ho-Chen,jj bustamanteJJ Bustamante,mj soaresMJ Soares,

    For similar cells: trophoblasts research abstracts see: cells: trophoblasts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Endocrinology

    VOLUME: 148

    Page Numbers: 559-65

    Journal Abbreviation: Endocrinology

    ISSN: 0013-7227

    DAY: 9

    MONTH: 11

    YEAR: 2006

    Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 375040

    Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Keywords Mesh Terms:

    KEYWORDS: Trophoblasts

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia. Information

    Substance Name: Oxygen

    Registry Number: 7782-44-7

    Grant and Affiliation Information for Prolactin-like protein-f subfamily of placental hormones/cytokines: responsiveness to maternal hypoxia.

    AFFILIATION: Institute of Maternal-Fetal Biology, Division of Cancer and Developmental Biology, Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NICHD

    GRANT: HD48861

    ACRONYM: HD

    MEDLINETA: Endocrinology

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER: BI276593

    Number Hits: 0

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