Rapid stimulation of cellular Pi uptake by the inositol pyrophosphate InsP8 induced by its photothermal release from lipid nanocarriers using a near infra-red light-emitting diode. Issue 37 (16th September 2020)

• Record Type: Journal Article
• Authors: Wang, Zhenzhen; Jork, Nikolaus; Bittner, Tamara; Wang, Huanchen; Jessen, Henning J.; Shears, Stephen B.
• Is Part Of: Chemical science. Volume 11:Issue 37(2020)
• Page Start: 10265
• Page End: 10278
• Publication Date: 2020-09-16
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc02144j
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Thermosensitive liposomes were used to deliver inositol pyrophosphates (highly polar, cell-impermeant signaling molecules) into cultured cells; cargo release was induced within 5 min irradiation by a high power, near infra-red, light emitting diode. Abstract : Inositol pyrophosphates (PP-InsPs), including diphospho- myo -inositol pentakisphosphate (5-InsP7 ) and bis-diphospho- myo -inositol tetrakisphosphate (1, 5-InsP8 ), are highly polar, membrane-impermeant signaling molecules that control many homeostatic responses to metabolic and bioenergetic imbalance. To delineate their molecular activities, there is an increasing need for a toolbox of methodologies for real-time modulation of PP-InsP levels inside large populations of cultured cells. Here, we describe procedures to package PP-InsPs into thermosensitive phospholipid nanocapsules that are impregnated with a near infra-red photothermal dye; these liposomes are readily accumulated into cultured cells. The PP-InsPs remain trapped inside the liposomes until the cultures are illuminated with a near infra-red light-emitting diode (LED) which permeabilizes the liposomes to promote PP-InsP release. Additionally, so as to optimize these procedures, a novel stably fluorescent 5-InsP7 analogue ( i.e., 5-FAM-InsP7 ) was synthesized with the assistance of click-chemistry; the delivery and deposition of the analogue inside cells was monitored by flow cytometry and by confocal microscopy. We describe quantitatively-controlled PP-InsP release inside cells within 5 min of LED irradiation, without measurable effect upon cell integrity, using a collimated 22 mm beam that can irradiate up to 10 6 cultured cells. Finally, to interrogate the biological value of these procedures, we delivered 1, 5-InsP8 into HCT116 cells and showed it to dose-dependently stimulate the rate of [ 33 P]-Pi uptake; these observations reveal a rheostatic range of concentrations over which 1, 5-InsP8 is biologically functional in Pi homeostasis.