scholarly journals Vascular bundle sheath and mesophyll regulation of leaf water balance in response to chitin

2018 ◽  
Author(s):  
Ziv Attia ◽  
Ahan Dalal ◽  
Menachem Moshelion

ABSTRACTPlants can detect pathogen invasion by sensing pathogen-associated molecular patterns (PAMPs). This sensing process leads to the induction of defense responses. Most PAMP mechanisms of action have been described in the guard cells. Here, we describe the effects of chitin, a PAMP found in fungal cell walls, on the cellular osmotic water permeability (Pf) of the leaf vascular bundle-sheath (BS) and mesophyll cells and its subsequent effect on leaf hydraulic conductance (Kleaf).The BS is a parenchymatic tissue that tightly encases the vascular system. BS cells have been shown to controlKleafthrough changes in theirPf, for example, in response to ABA. It was recently reported that, in Arabidopsis, the chitin receptors chitin elicitor receptor kinase 1 (CERK1) and LYSINE MOTIF RECEPTOR KINASE 5 (LYK5) are highly expressed in the BS, as well as the neighboring mesophyll. Therefore, we studied the possible impact of chitin on these cells.Our results revealed that both BS cells and mesophyll cells exhibit a sharp decrease inPfin response to chitin treatment. In addition, xylem-fed chitin decreasedKleafand led to stomatal closure. However, anAtlyk5mutant showed none of these responses. ComplimentingAtLYK5specifically in the BS cells (using the SCARECROW promoter) and transient expresion in mesophyll cells each resulted in a response to chitin that was similar to that observed in the wild type. These results suggest that BS and mesophyll cells each play a role in the perception of apoplastic chitin and in initiating chitin-triggered immunity.Significance StatementPAMP perception by plant receptors triggers various defense responses important for plant immunity. Here we provide new insights into a topic that has received a great deal of previous attention, revealing that a chitin immune response is present in additional leaf tissues other than the stomata. Chitin perception by the bundle sheath cells enwrapping the whole leaf vascular system decrease its cellular osmotic permeability and leaf hydraulic conductance. This in turn, leads to hydraulic signals being sent to the stomata and regulates whole-leaf water balance in response to chitin application and, perhaps, during fungal infection. Emphasizing the dynamic role of the BS in chitin-sensing and water balance regulation.

2019 ◽  
Vol 101 (6) ◽  
pp. 1368-1377 ◽  
Author(s):  
Ziv Attia ◽  
Ahan Dalal ◽  
Menachem Moshelion

2017 ◽  
Author(s):  
Yael Grunwald ◽  
Noa Wigoda ◽  
Nir Sade ◽  
Adi Yaaran ◽  
Tanmayee Torne ◽  
...  

AbstractThe leaf vascular bundle sheath cells (BSCs) that tightly envelop the leaf veins, are a selective and dynamic barrier to xylem-sap water and solutes radially entering the mesophyll cells. Under normal conditions, xylem-sap pH of <6 is presumably important for driving and regulating the transmembranal solute transport. Having discovered recently a differentially high expression of a BSCs proton pump, AHA2, we now test the hypothesis that it regulates this pH and leaf radial water fluxes.We monitored the xylem-sap pH in the veins of detached leaves of WT Arabidopsis, AHA mutants, and aha2 mutants complemented with AHA2 gene solely in BSCs. We tested an AHA inhibitor and stimulator, and different pH buffers. We monitored their impact on the xylem-sap pH and the whole leaf hydraulic conductance (Kleaf), and the effect of pH on the water osmotic permeability (Pf) of isolated BSCs protoplasts.Our results demonstrated that AHA2 is necessary for xylem-sap acidification, and in turn, for elevating Kleaf. Conversely, knocking out AHA2 alkalinized the xylem-sap. Also, elevating xylem sap pH to 7.5 reduced Kleaf and elevating external pH to 7.5 decreased the BSCs Pf.All these demonstrate a causative link between AHA2 activity in BSCs and leaf radial water conductance.One-sentence summaryBundle-sheath cells can control the leaf hydraulic conductance by proton-pump-regulated xylem sap pH


1969 ◽  
Vol 44 (6) ◽  
pp. 826-830 ◽  
Author(s):  
A. R. G. Lang ◽  
Betty Klepper ◽  
Malcolm J. Cumming

1984 ◽  
Vol 62 (4) ◽  
pp. 812-817 ◽  
Author(s):  
Maria Emília Estelita-Teixeira ◽  
Walter Handro

Ultrastructural aspects, especially the organization of chloroplasts and their distribution, were studied in leaves of three species of Gomphrena (G. macrocephala, G. prostrata, and G. decipiens) presenting "Kranz anatomy," and in Pfaffia jubata, without that characteristic. In Gomphrena spp. the distribution of chloroplasts according to the complexity of their lamellar system seems to follow a gradient: most of the chloroplasts in the bundle sheath cells have poorly developed grana but some of them, in the cell side opposite to the vascular bundle, may present conspicuous grana. A similar situation occurs in "Kranz mesophyll cells," but in this case grana are more developed. Finally, chloroplasts in "non-Kranz mesophyll cells" have the more developed grana. In P. jubata no differences occur in chloroplast structure, all of them showing well-organized grana. Chloroplasts with well-developed grana were found in vascular parenchyma and in companion cells of Gomphrena spp. and P. jubata.


Plant Ecology ◽  
2014 ◽  
Vol 215 (11) ◽  
pp. 1255-1267 ◽  
Author(s):  
Mei Sun ◽  
Shi-Jian Yang ◽  
Jiao-Lin Zhang ◽  
Megan Bartlett ◽  
Shi-Bao Zhang

2019 ◽  
Author(s):  
Yael Grunwald ◽  
Sanbon Chaka Gosa ◽  
Tanmayee Torne ◽  
Nava Moran ◽  
Menachem Moshelion

ABSTRACTThe leaf vascular bundle sheath cells (BSCs), which tightly envelop the leaf veins, constitute a selective dynamic barrier to water and solutes radially entering the mesophyll and play a major role in regulating the leaf radial hydraulic conductance (Kleaf). Recently, we showed that the BSCs’ plasma membrane H+-ATPase, AHA2, increases Kleaf by acidifying the xylem sap. Since BL reportedly increases Kleaf and we found the blue light (BL) receptor genes, PHOT1 and PHOT2 expressed in the Arabidopsis BSCs, we hypothesized that, similar to the guard cells (GCs) BL signal transduction pathway, the BSCs’ PHOT1 and PHOT2 activate the BSCs’ H+-ATPase and thus regulate Kleaf. Indeed, under BL illumination, the Kleaf in the knockout mutant lines phot1-5, phot2-1, phot1-5phot2-1 and aha2-4 was lower than in WT. BSCs-directed complementation (using the SCR promoter) of phot1-5 and aha2-4 respectively by PHOT1 and AHA2, restored the BL-induced Kleaf increase. BSCs-specific silencing of PHOT1 or PHOT2 (using the SCR promoter) abolished the BL-induced Kleaf increase. Xylem-fed PHOT inhibitor, tyrphostin 9, also abolished the BL-induced Kleaf increase in WT. Moreover, in WT plants, white light (WL) acidified the xylem sap compared to dark, but did not acidify the xylem sap of the phot1-5 mutant. BSCs-specific complementation of phot1-5 by SCR: PHOT1, restored the WL-induced xylem acidification. On a cellular level, BL hyperpolarized the BSCs, which was prevented by tyrphostin 9. In addition, the osmotic water permeability coefficient (Pf) of the BSCs was higher under WL treatment. Our results link the blue light control of water fluxes from the xylem to the mesophyll via the BSCs in the following model:BL →BSCs’ PHOTs activation →tyrosine phosphorylation→BSCs’ H+- ATPase activation →BSCs hyperpolarization, xylem acidification →Pf elevation → Kleaf increase. Thus, this study is the first to demonstrate an independent BL signal transduction pathway regulation of the vascular tissue.


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