Artículos de revistas
Phospholipase D2:A Pivotal Player Modulating RBL-2H3 Mast Cell Structure
Fecha
2012Registro en:
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, LONDON, v. 60, n. 5, supl. 1, Part 6, pp. 386-396, MAY, 2012
0022-1554
10.1369/0022155412438886
Autor
Meirelles Marchini-Alves, Claudia Maria
Nicoletti, Liliana Martos
Mazucato, Vivian Marino
de Souza, Lorena Brito
Hitomi, Tomohiro
Alves, Cleidson de Padua
Jamur, Maria Celia
Oliver, Constance
Institución
Resumen
The current study examined the role of PLD2 in the maintenance of mast cell structure. Phospholipase D (PLD) catalyzes hydrolysis of phosphatidylcholine to produce choline and phosphatidic acid (PA). PLD has two isoforms, PLD1 and PLD2, which vary in expression and localization depending on the cell type. The mast cell line RBL-2H3 was transfected to overexpress catalytically active (PLD2CA) and inactive (PLD2CI) forms of PLD2. The results of this study show that PLD2CI cells have a distinct star-shaped morphology, whereas PLD2CA and RBL-2H3 cells are spindle shaped. In PLD2CI cells, the Golgi complex was also disorganized with dilated cisternae, and more Golgi-associated vesicles were present as compared with the PLD2CA and RBL-2H3 cells. Treatment with exogenous PA led to the restoration of the wild-type Golgi complex phenotype in PLD2CI cells. Conversely, treatment of RBL-2H3 and PLD2CA cells with 1% 1-Butanol led to a disruption of the Golgi complex. The distribution of acidic compartments, including secretory granules and lysosomes, was also modified in PLD2CI cells, where they concentrated in the perinuclear region. These results suggest that the PA produced by PLD2 plays an important role in regulating cell morphology in mast cells. (J Histochem Cytochem 60:386-396, 2012)