Title of article :
Role of Intracellular Divalent Cations on the Adenylate Cyclase Activation by Human LH in mLTC-1 Leydig Cells
Author/Authors :
Diep Nguyen, Thi Mong Department of Applied Biology & Agriculture - Faculty of Natural Sciences - Quy Nhon University, Binh Dinh, Vietnam , Giang Tran, Van Faculty of Biology - Hue University of Education - Hue University, Hue, Vietnam , Hieu Nguyen, Thi Chi Faculty of Applied Biology - Quang Trung University, Quy Nhon, Vietnam , Nguyen, Ba Nghi Faculty of Applied Biology - Quang Trung University, Quy Nhon, Vietnam
Abstract :
activation. The activated GsαGTP subunit stimulates Adenylyl Cyclase (ACs) and, therefore, intracellular cyclic Adenosine Monophosphate (cAMP) accumulation from the AC substrate Adenosine Triphosphate (ATP). The divalent cations, magnesium (Mg2+) or manganese (Mn2+) associate with ATP to form the real substrates of ACs. In addition, ACs are sensitive to calcium (Ca2+) but in a different way than Mg2+ or Mn2+. Indeed, LH increases the cytoplasmic calcium ion concentration ([Ca2+]cyt) but only when Ca2+ is present in the extracellular medium.
Materials and Methods: In the present study, the effects of intracytoplasmic Ca2+, Mg2+, and Mn2+ on the cyclic AMP response to human LH in mLTC-1 Leydig tumor cells were investigated. The mLTC-1 cells were incubated at 37 °C in media supplemented with and without 5 μM Ca2+, 5 μM Mg2+, or 5 μM Mn2+. The intracellular cyclic AMP accumulation was then monitored under LH stimulation.
Results: Our findings revealed that only Mg2+ and Mn2+ in the extracellular medium potentiate the cAMP response to hLH, in contrast to Ca2+. In addition, we also showed that HCO3- increased the stimulation of the adenylyl cyclase enzyme by Ca2+, Mg2+ or Mn2+.
Conclusions: In mLTC-1 cells, extracellular Mg2+ and Mn2+ might potentiate LH-stimulated ACs activity by favoring LH interaction with its receptor, whereas Ca2+ from internal stores might be mobilized towards the cytoplasm to increase ACs activity, possibly through the soluble isoform.
Keywords :
Adenosine Monophosphate , Adenylyl Cyclase , mLTC-1 , Luteinizing Hormone , Forskolin
Journal title :
Journal of Applied Biotechnology Reports