ER-mitochondria tethering by PDZD8 regulates Ca(2+) dynamics in mammalian neurons

PDZD8介导的内质网-线粒体连接调节哺乳动物神经元中的Ca(2+)动态变化

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Abstract

Interfaces between organelles are emerging as critical platforms for many biological responses in eukaryotic cells. In yeast, the ERMES complex is an endoplasmic reticulum (ER)-mitochondria tether composed of four proteins, three of which contain a SMP (synaptotagmin-like mitochondrial-lipid binding protein) domain. No functional ortholog for any ERMES protein has been identified in metazoans. Here, we identified PDZD8 as an ER protein present at ER-mitochondria contacts. The SMP domain of PDZD8 is functionally orthologous to the SMP domain found in yeast Mmm1. PDZD8 was necessary for the formation of ER-mitochondria contacts in mammalian cells. In neurons, PDZD8 was required for calcium ion (Ca(2+)) uptake by mitochondria after synaptically induced Ca(2+)-release from ER and thereby regulated cytoplasmic Ca(2+) dynamics. Thus, PDZD8 represents a critical ER-mitochondria tethering protein in metazoans. We suggest that ER-mitochondria coupling is involved in the regulation of dendritic Ca(2+) dynamics in mammalian neurons.

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