12/14/2022 0 Comments Machacha nyc![]() ![]() STIM1 is the ER Ca2+ sensor that detects Ca2+ store depletion and activates the plasma membrane channel Orai1. This includes the basic molecular regulation of the two key molecules in SOCE, STIM1 and Orai1. Ongoing projects in the Lab are focused on understanding the regulation of IP3-dependent Ca2+ release and store-operated Ca2+ entry (SOCE) during the meiotic cell cycle. Such remodeling includes the IP3-dependent Ca2+ release, the plasma membrane Ca2+-ATPase at the cell membrane, and store-operated Ca2+ entry (see Figure). We are interested in the mechanisms mediating this molecular remodeling of Ca2+ signals during meiotic maturation. This is a physiologically attractive model because a Ca2+ signal at fertilization is the universal trigger to induce egg activation in all sexually reproducing species tested to date. Before fertilization competent oocytes undergo a maturation period - oocyte maturation - which encompasses entry into meiosis and dramatic remodeling of Ca2+ signaling pathways. We have discovered that transition metal chelation arrests the meiotic cell cycle through interfering with the function of the dual specificity phosphatase Cdc25C, a central player in the regulation of meiotic progression.We have a long standing interest in the regulation and remodeling of Ca2+ signaling pathways during the meiotic cell cycle. We are also interested in the regulation of the cell division phase by transition metals. Our interest in the basic cellular and molecular mechanisms of Ca2+ signaling is framed in the context of several projects that the Lab is presently focused on. Ca2+ signals are ubiquitous and are involved in a plethora of cell physiological processes including fertilization, cell proliferation, and gene expression. The Machaca Lab is interested in the regulation of Ca2+ signaling pathways under both physiological and pathological conditions.
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