Fig. 11. A model depicting the functional interactions between ER and mitochondria
in the mouse egg. After Ca2+ is released from the ER into the
cytosol via Ins(1,4,5)P3 receptors it can be taken up by
the mitochondria. In the mitochondrial matrix, Ca2+ will stimulate
the Krebs cycle as well as the electron transport chain and the
F0/F1 synthase that phosphorylates ADP. ATP is then
transported out of the mitochondria via the activity of the adenine nucleotide
translocase (ANT) and the cytosolic ATP will be consumed by the SERCA pumps to
restore the resting [Ca2+]c and refill the ER.