Transport of casein submicelles and formation of secretion granules in the Golgi apparatus of epithelial cells of the lactating mammary gland of the rat
- PMID: 8430906
- DOI: 10.1002/ar.1092350305
Transport of casein submicelles and formation of secretion granules in the Golgi apparatus of epithelial cells of the lactating mammary gland of the rat
Abstract
Lactating mammary glands fixed by perfusion with 5% glutaraldehyde subsequently were postfixed with potassium ferrocyanide reduced osmium or were treated with tannic acid. Stained thin sections were examined with the electron microscope and stereopairs were prepared. The distribution of casein submicelles was analyzed in the various components of the Golgi apparatus. The Golgi stacks were composed of five or six elements, all of which contained casein submicelles 20 nm in diameter. The cis-tubular network or cis-element, as well as the underlying three or four midsaccules, showed these casein submicelles either attached to their membrane or free in the lumen. The trans-most element of the stacks formed distended prosecretory granules in which both isolated or clustered casein submicelles were suspended in an electron-lucent fluid. These micellar aggregates increased in size and became progressively more compact to form spherical dense bodies or casein micelles, in which the individual 20 nm particles could easily be resolved. Casein micelles were seen in secretory granules in addition to a wispy material of low density. The numerous small spherical vesicles (80 nm or larger) seen on the cis, lateral, or trans aspects of the stacks did not appear to contain free casein submicelles. This raises questions regarding the role of these vesicles in the transport of casein macromolecules through the Golgi stacks. It was noticeable that in this Golgi apparatus a trans-Golgi network was limited to a few small residual tubules free from casein submicelles. It thus appears that the greater part of the trans-most Golgi element gives rise to the large prosecretory granules. After leaving the Golgi region and prior to exocytosis, the secretory granules often fuse to form larger granules before exocytosis.
Similar articles
-
Structure of the Golgi apparatus in stimulated and nonstimulated acinar cells of mammary glands of the rat.Anat Rec. 1993 Nov;237(3):308-17. doi: 10.1002/ar.1092370303. Anat Rec. 1993. PMID: 8291683
-
Tridimensional architecture of the Golgi apparatus and its components in mucous cells of Brunner's glands of the mouse.Am J Anat. 1987 Jun;179(2):95-107. doi: 10.1002/aja.1001790202. Am J Anat. 1987. PMID: 3039824
-
Formation of secretion granules in the Golgi apparatus of pancreatic acinar cells of the rat.Am J Anat. 1988 Nov;183(3):187-99. doi: 10.1002/aja.1001830302. Am J Anat. 1988. PMID: 2850745
-
Trans-Golgi network (TGN) of different cell types: three-dimensional structural characteristics and variability.Anat Rec. 1995 Jul;242(3):289-301. doi: 10.1002/ar.1092420302. Anat Rec. 1995. PMID: 7573976 Review.
-
The biological significance of storage granules in rat parathyroid cells.Microsc Res Tech. 1995 Oct 1;32(2):148-63. doi: 10.1002/jemt.1070320209. Microsc Res Tech. 1995. PMID: 8580509 Review.
Cited by
-
AlphaS1-casein, which is essential for efficient ER-to-Golgi casein transport, is also present in a tightly membrane-associated form.BMC Cell Biol. 2010 Aug 12;11:65. doi: 10.1186/1471-2121-11-65. BMC Cell Biol. 2010. PMID: 20704729 Free PMC article.
-
Regulation of secretory granule size by the precise generation and fusion of unit granules.J Cell Mol Med. 2010 Jul;14(7):1904-16. doi: 10.1111/j.1582-4934.2010.01071.x. Epub 2010 Apr 19. J Cell Mol Med. 2010. PMID: 20406331 Free PMC article. Review.
-
Calcium secretion into milk.J Mammary Gland Biol Neoplasia. 2005 Apr;10(2):119-28. doi: 10.1007/s10911-005-5395-z. J Mammary Gland Biol Neoplasia. 2005. PMID: 16025219 Review.
-
Models of Intracellular Transport: Pros and Cons.Front Cell Dev Biol. 2019 Aug 7;7:146. doi: 10.3389/fcell.2019.00146. eCollection 2019. Front Cell Dev Biol. 2019. PMID: 31440506 Free PMC article.
-
ZnT4 provides zinc to zinc-dependent proteins in the trans-Golgi network critical for cell function and Zn export in mammary epithelial cells.Am J Physiol Cell Physiol. 2012 Aug 1;303(3):C291-7. doi: 10.1152/ajpcell.00443.2011. Epub 2012 May 23. Am J Physiol Cell Physiol. 2012. PMID: 22621784 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources