» Articles » PMID: 6436254

Differences in the Behavior of Cytoplasmic Granules and Lipid Bodies During Human Lung Mast Cell Degranulation

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1984 Nov 1
PMID 6436254
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

We used a morphometric and autoradiographic approach to analyze changes in specific cytoplasmic granules and cytoplasmic lipid bodies associated with human lung mast cell degranulation. Mast cells were dissociated from lung tissue by enzymatic digestion and were then enriched to purities of up to 99% by countercurrent centrifugation elutriation and recovery from columns containing specific antigen bound to Sepharose 6 MB. Degranulation was induced by goat anti-IgE. At various intervals after stimulation, parallel aliquots of cells were recovered for determination of histamine release or were fixed for transmission electron microscopy. We found that lipid bodies, electron-dense structures that lack unit membranes, were present in both control and stimulated mast cells. Autoradiographic analysis showed that lipid bodies represented the major repository of 3H-label derived from [3H]arachidonic acid taken up from the external milieu. By contrast, the specific cytoplasmic granules contained no detectable 3H-label. In addition, lipid bodies occurred in intimate association with degranulation channels during mast cell activation, but the total volume of lipid bodies did not change during the 20 min after stimulation with anti-IgE. This result stands in striking contrast to the behavior of specific cytoplasmic granules, the great majority of which (77% according to aggregate volume) exhibited ultrastructural alterations during the first 20 min of mast cell activation. These observations establish that mast cell cytoplasmic granules and cytoplasmic lipid bodies are distinct organelles that differ in ultrastructure, biochemistry, and behavior during mast cell activation.

Citing Articles

Immunohistochemical Expression of Vascular Endothelial Growth Factor (VEGF) in Primary Canine Mast Cell Tumors and Related Regional Lymph Node Metastasis.

Correa Rassele A, Oliveira Almeida I, Garschagen Gava M, Bronhara Pimentel P, Giuliano A, Ruiz Sueiro F Animals (Basel). 2025; 15(2).

PMID: 39858283 PMC: 11761284. DOI: 10.3390/ani15020283.


Degranulation of human mast cells: modulation by P2 receptors' agonists.

Schulman E, Nishi H, Pelleg A Front Immunol. 2023; 14:1216580.

PMID: 37868982 PMC: 10585249. DOI: 10.3389/fimmu.2023.1216580.


Development of Human Mast Cells from Hematopoietic Stem Cells within a 3D Collagen Matrix: Effect of Stem Cell Media on Mast Cell Generation.

Derakhshan T, Bhowmick R, Ritchey J, Gappa-Fahlenkamp H Stem Cells Int. 2018; 2018:2136193.

PMID: 30123284 PMC: 6079339. DOI: 10.1155/2018/2136193.


Comparative analysis of lipotoxicity induced by endocrine, pharmacological, and innate immune stimuli in rat basophilic leukemia cells.

Maaetoft-Udsen K, Greineisen W, Aldan J, Magaoay H, Ligohr C, Shimoda L J Immunotoxicol. 2014; 12(4):385-94.

PMID: 25539471 PMC: 4755781. DOI: 10.3109/1547691X.2014.990655.


Mast cells: from lipid droplets to lipid mediators.

Dichlberger A, Kovanen P, Schneider W Clin Sci (Lond). 2013; 125(3):121-30.

PMID: 23577635 PMC: 3631086. DOI: 10.1042/CS20120602.


References
1.
BRINKMAN G . The mast cell in normal human bronchus and lung. J Ultrastruct Res. 1968; 23(1):115-23. DOI: 10.1016/s0022-5320(68)80035-8. View

2.
Kobayasi T, Midtgard K, ASBOE-HANSEN G . Ultrastructure of human mast-cell granules. J Ultrastruct Res. 1968; 23(1):153-65. DOI: 10.1016/s0022-5320(68)80039-5. View

3.
Rohlich P, Anderson P, UVNAS B . Electron microscope observations on compounds 48-80-induced degranulation in rat mast cells. Evidence for sequential exocytosis of storage granules. J Cell Biol. 1971; 51(21):465-83. PMC: 2108143. DOI: 10.1083/jcb.51.2.465. View

4.
Lagunoff D . Contributions of electron microscopy to the study of mast cells. J Invest Dermatol. 1972; 58(5):296-311. DOI: 10.1111/1523-1747.ep12540314. View

5.
Dvorak A, Hammond M, Dvorak H, Karnovsky M . Loss of cell surface material from peritoneal exudate cells associated with lymphocyte-mediated inhibition of macrophage migration from capillary tubes. Lab Invest. 1972; 27(6):561-74. View