Associating Wound-Related Changes in the Apoplast Proteome of Medicago with Early Steps in the ROS Signal-Transduction Pathway

Early wound-related changes in the leaf apoplast proteome of Medicago truncatula have been characterized by 2-DE and MALDI-TOF/TOF and the differential expression of 28/110 extracellular proteins could be reproducibly observed 6 h after wounding. Wounding induced an initial (0−30 min) burst of O 2 −, followed by a later (3−6 h) production of O 2 − and H 2 O 2 . The infiltration of 5 μM DPI ≤ 3 min after wounding inhibited both phases of the oxidative burst and suppressed wound-regulated changes in 9/28 extracellular proteins. DPI infiltrated 15 min after wounding only partially inhibited early O 2 − production and was ineffective in suppressing wound-related changes in these proteins. This strongly suggests that in wounded Medicago, rapid O 2 − is required for mobilizing the downstream (3−6 h), differential expression of several extracellular proteins. Further studies with DPI and exogenous sources of ROS supported the regulation of these proteins within early, wound-related ROS-signaling events. The study forms the basis for associating wound-related changes in the apoplast proteome with ROS-dependent and ROS-independent pathways. Proteins mobilized within the ROS-dependent pathway were largely ionically bound to cell walls and included SODs, peroxidases and germin-like proteins, suggesting their involvement within wound-activated, ROS regulatory loops.