Expression of fibroblast growth factor 10 and its receptor, fibroblast growth factor receptor 2B, in the bovine corpus luteum
Autor: | I. C. Giometti, Bajram Berisha, Paula de Carvalho Papa, Anthony C. S. Castilho, Jose Buratini, Renée Laufer Amorim, Dieter Schams, Christopher A. Price |
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Rok vydání: | 2008 |
Předmět: |
medicine.medical_specialty
Time Factors Luteolysis Biology Dinoprost Fibroblast growth factor Andrology Corpus Luteum Oxytocics Internal medicine Fibroblast Growth Factor Receptor 2b Genetics medicine Animals Receptor Fibroblast Growth Factor Type 2 Receptor Messenger RNA FGF10 Reverse Transcriptase Polymerase Chain Reaction Cell Biology Immunohistochemistry stomatognathic diseases medicine.anatomical_structure Endocrinology Gene Expression Regulation Cattle Female Fibroblast Growth Factor 10 Corpus luteum Signal Transduction Developmental Biology |
Zdroj: | Molecular Reproduction and Development. 75:940-945 |
ISSN: | 1098-2795 1040-452X |
Popis: | There is evidence that several fibroblast growth factors (FGFs) are involved in growth and development of the corpus luteum (CL), but many FGFs have not been investigated in this tissue, including FGF10. The objective of this study was to determine if FGF10 and its receptor (FGFR2B) are expressed in the CL. Bovine CL were collected from an abattoir and classed as corpus hemorrhagica (stage I), developing (stage II), developed (stage III), and regressed (stage IV) CL. Expression of FGF10 and FGFR2B mRNA was measured by reverse transcription-polymerase chain reaction (RT-PCR). Both genes were expressed in bovine CL, and FGF10 expression did not differ between stages of CL development. FGF10 protein was localized to large and small luteal cells by immunohistochemistry. FGFR2B expression was approximately threefold higher in regressed compared to developing and developed CL (P < 0.05). To determine if FGF10 and FGFR2B expression is regulated during functional luteolysis, cattle were injected with PGF2alpha and CL collected at 0, 0.5, 2, 4, 12, 24, 48, and 64 hr thereafter (n = 5 CL/time point), and mRNA abundance was measured by real-time RT-PCR. FGF10 mRNA expression did not change during functional luteolysis, whereas FGFR2B mRNA abundance decreased significantly at 2, 4, and 12 hr after PGF2alpha, and returned to pretreatment levels for the period 24-64 hr post-PGF2alpha. These data suggest a potential role for FGFR2B signaling during structural luteolysis in bovine CL. |
Databáze: | OpenAIRE |
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