An Autocrine Negative Feedback Loop Inhibits Dictyostelium discoideum Proliferation through Pathways Including IP3/Ca 2+
Author(s) -
Yu Tang,
Ramesh Rijal,
David E. Zimmerhanzel,
Jacquelyn McCullough,
Louis A. Cadena,
Richard H. Gomer
Publication year - 2021
Publication title -
mbio
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.562
H-Index - 121
eISSN - 2161-2129
pISSN - 2150-7511
DOI - 10.1128/mbio.01347-21
Subject(s) - dictyostelium discoideum , microbiology and biotechnology , tensin , biology , inositol , phospholipase c , signal transduction , pten , guanine nucleotide exchange factor , phosphoinositide phospholipase c , ras superfamily , polyphosphate , phosphatase , small gtpase , biochemistry , receptor , phosphorylation , gtp' , pi3k/akt/mtor pathway , enzyme , phosphate , gene
Little is known about how eukaryotic cells can sense their number or spatial density and stop proliferating when the local density reaches a set value. We previously found that Dictyostelium discoideum accumulates extracellular polyphosphate to inhibit its proliferation, and this requires the G protein-coupled receptor GrlD and the small GTPase RasC. Here, we show that cells lacking the G protein component Gβ, the Ras guanine nucleotide exchange factor GefA, phosphatase and tensin homolog (PTEN), phospholipase C (PLC), inositol 1,4,5-trisphosphate (IP3) receptor-like protein A (IplA), polyphosphate kinase 1 (Ppk1), or the TOR complex 2 component PiaA have significantly reduced sensitivity to polyphosphate-induced proliferation inhibition. Polyphosphate upregulates IP3, and this requires GrlD, GefA, PTEN, PLC, and PiaA. Polyphosphate also upregulates cytosolic Ca 2+ , and this requires GrlD, Gβ, GefA, RasC, PLC, IplA, Ppk1, and PiaA. Together, these data suggest that polyphosphate uses signal transduction pathways including IP3/Ca 2+ to inhibit the proliferation of D. discoideum .
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