Section of Cellular Signaling, Department of Molecular Biophysics and Physiology, Rush University, 1750 Chicago, IL 60612, USA.
J Physiol Sci. 2010 Jan;60(1):81-4. doi: 10.1007/s12576-009-0069-z. Epub 2009 Nov 26.
Many molecular biological interventions in current use, as well as inheritable disease conditions, modify the intracellular endowment of molecules that bind Ca(2+) or channels and pumps that transfer it to and from intracellular storage organelles. A simple law, named the "cell boundary theorem," states that intracellular alterations cannot directly result in changes in the cytosolic concentration, Ca(2+), in a true resting state. A demonstration of the validity of this theorem is provided. Several examples are then discussed of interventions or diseases that increase leak of Ca(2+) from storage organelles and result in greater resting Ca(2+). According to the theorem, the increase in Ca(2+) cannot be a direct consequence of the greater leak. Its primary cause must be a change of the fluxes at the level of the plasmalemma, caused in turn by the increase in leak through some sort of "store-operated Ca(2+) entry." While the law is discussed in terms of Ca(2+) homeostasis, it applies to any solute that may be transported by the plasma membrane.
许多目前使用的分子生物学干预措施,以及遗传性疾病状况,都会改变结合 Ca(2+) 的细胞内分子的赋存,或者改变将其从细胞内储存细胞器转运到其中和从中转运的通道和泵。一条简单的定律,称为“细胞边界定理”,指出在真正的静息状态下,细胞内的改变不能直接导致细胞溶质浓度 Ca(2+) 的变化。该定理的有效性提供了一个证明。然后讨论了几种干预措施或疾病,这些措施或疾病会增加 Ca(2+) 从储存细胞器的渗漏,并导致更大的静息 Ca(2+)。根据该定理,Ca(2+) 的增加不能直接归因于更大的渗漏。其主要原因必须是质膜水平上的通量发生了变化,这反过来又是由于通过某种“储存操纵的 Ca(2+) 内流”而增加的渗漏引起的。虽然该定律是根据 Ca(2+) 动态平衡来讨论的,但它适用于任何可能通过质膜转运的溶质。