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The role of adrenergic activation on murine luteal cell viability and progesterone production  Jing Wang, Min Tang, Huaide Jiang, Bing Wu, Wei Cai, Chuan.

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Presentation on theme: "The role of adrenergic activation on murine luteal cell viability and progesterone production  Jing Wang, Min Tang, Huaide Jiang, Bing Wu, Wei Cai, Chuan."— Presentation transcript:

1 The role of adrenergic activation on murine luteal cell viability and progesterone production 
Jing Wang, Min Tang, Huaide Jiang, Bing Wu, Wei Cai, Chuan Hu, Riqiang Bao, Qiming Dong, Li Xiao, Gang Li, Chunping Zhang  Theriogenology  Volume 86, Issue 5, Pages (September 2016) DOI: /j.theriogenology Copyright © 2016 Elsevier Inc. Terms and Conditions

2 Fig. 1 The influence of NE and ISO on murine luteal cell viability. (A) MTT assay for the cultured luteal cells with control, 1-μM NE, 10-μM NE, and 100-μM NE after 2-day culture. (B) MTT assay for the cultured luteal cells with control, 1-μM ISO, 10-μM ISO, and 100-μM ISO after 2-day culture. * P < 0.05. (C) The primary luteal cells with control, 100-μM NE, and 100-μM ISO after 2-day culture. Scale bar, 50 μm. (D) The apoptosis of luteal cells after treatment with control, 100-μM NE, and 100-μM ISO after 2-day culture. Scale bar, 100 μm. ISO, isoprenaline; MTT, (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; NE, norepinephrine. Theriogenology  , DOI: ( /j.theriogenology ) Copyright © 2016 Elsevier Inc. Terms and Conditions

3 Fig. 2 The effect of propranolol on murine luteal cell viability induced by NE and ISO. (A) MTT assay for the cultured luteal cells with control, 100-μM NE, 10-μM propranolol, and 100-μM NE + 10-μM propranolol after 2-day culture. (B) MTT assay for the cultured luteal cells with control, 100-μM ISO, 10-μM propranolol, and 100-μM ISO + 10-μM propranolol after 2-day culture. * P < 0.05. ISO, isoprenaline; MTT, (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; NE, norepinephrine. Theriogenology  , DOI: ( /j.theriogenology ) Copyright © 2016 Elsevier Inc. Terms and Conditions

4 Fig. 3 The expression of genes in luteal cells was assessed by Real-time polymerase chain reaction. (A) shows that CyclinD2 messenger RNA (mRNA) was increased and Caspase3 mRNA was decreased after treatment with NE. (B) shows that Caspase3 mRNA was decreased and PGF2α was increased after treatment with ISO. * P < 0.05. ISO, isoprenaline; NE, norepinephrine; PGF2α, prostaglandin F2α. Theriogenology  , DOI: ( /j.theriogenology ) Copyright © 2016 Elsevier Inc. Terms and Conditions

5 Fig. 4 The effect of NE and ISO on estradiol and progesterone secretion in luteal cells. The estradiol and progesterone was measured using radioimmunoassay. (A) and (B) showed the estradiol and progesterone content in cultured media, respectively, after treatment with 100-μM NE and 100-μM ISO. (C) showed that the effect of propranolol on progesterone production induced by NE and ISO. * P < 0.05. ISO, isoprenaline; NE, norepinephrine. Theriogenology  , DOI: ( /j.theriogenology ) Copyright © 2016 Elsevier Inc. Terms and Conditions

6 Fig. 5 The messenger RNA (mRNA) and protein level of steroidogenic-related enzymes in luteal cells was assessed by real-time polymerase chain reaction and Western blotting. (A) showed the mRNA level of LHR, StAR, and 3β-HSD in luteal cells after treatment with 100-μM NE and 100-μM ISO. (B) showed the protein level of StAR and 3β-HSD in luteal cells after treatment with 100-μM NE and 100-μM ISO. * P <  β-HSD, 3β-hydroxysteroid dehydrogenase; ISO, isoprenaline; NE, norepinephrine. Theriogenology  , DOI: ( /j.theriogenology ) Copyright © 2016 Elsevier Inc. Terms and Conditions


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