Since, the primordial Na-pump on the plasma membrane is the ultimate source of energy of animal cells; it appears that the remaining Ca-signaling networks will join the leading Na-pump, and the potential energy is used by remaining networks for homeostasis. Hence, the cellular bioenergetics initiated and managed by the NaAF regulated Na-pump, by turn regulated by the provisional Ca-pump and Ca-signaling, is the leading-center of a cell’s holistic-networks.

We visualized operation of the ion-pump under Ca-signaling as an all-time allosteric dancing of the Na-pump.  During operation, the ubiquitous NaAF acts as the dancing-partner cum gate-keeper of the double-gated (two α-subunits) Na-pump allowing simultaneous transport of Na (in) and K (out), while the process is controlled by Ca-signaling. Intensity of the dancing will be affected by the isoform-nature of the Na, K-ATPase which varies in various bodily cells in a tissue-specific manner except brain where the Na-pump is area-specific. The extremely specialized functions of the area-specific brain (of human) are of prime interests now-a-days.

The Ca-signaling is conducted periodically by the provisional Ca-pump which is an altered form of the cell-specific Na-pump. The provisional Ca-pump is entrusted to pump out the excess (inhibitory) local Ca for continuation of Na-pump function for homeostasis, thus making it a stop-and-go type dance.

This brings us to the question we are asking. Are the molecular natures of the provisional Ca-pumps the same as the isoforms of the PMCA well-known in the vast Ca-ATPase literature?

It will be very interesting issue to investigate. 

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