TFEB-mediated increase in peripheral lysosomes regulates store-operated calcium entry

Lysosomes are membrane-bound organelles mainly involved in catabolic processes. In addition, lysosomes can expel their contents outside of the cell via lysosomal exocytosis. Some of the key steps involved in these important cellular processes, such as vesicular fusion and trafficking, require calcium (Ca(2+)) signaling. Recent data show that lysosomal functions are transcriptionally regulated by transcription factor EB (TFEB) through the induction of genes involved in lysosomal biogenesis and exocytosis. Given these observations, we investigated the roles of TFEB and lysosomes in intracellular Ca(2+) homeostasis. We studied the effect of transient modulation of TFEB expression in HeLa cells by measuring the cytosolic Ca(2+) response after capacitative Ca(2+) entry activation and Ca(2+) dynamics in the endoplasmic reticulum (ER) and directly in lysosomes. Our observations show that transient TFEB overexpression significantly reduces cytosolic Ca(2+) levels under a capacitative influx model and ER re-uptake of calcium, increasing the lysosomal Ca(2+) buffering capacity. Moreover, lysosomal destruction or damage abolishes these TFEB-dependent effects in both the cytosol and ER. These results suggest a possible Ca(2+) buffering role for lysosomes and shed new light on lysosomal functions during intracellular Ca(2+) homeostasis.