Dense granules (also known as dense bodies or delta granules) are specialized secretory organelles. Dense granules are found only in platelets and are smaller than α-granules. The origin of these dense granules is still unknown, however, it is thought that may come from the mechanism involving the endocytotic pathway. Dense granules are a sub group of lysosome-related organelles (LRO). There are about three to eight of these in a normal human platelet.
In unicellular organisms
In multicellular organisms
The dense granules of human platelets contain adenosine diphosphate (ADP), adenosine triphosphate (ATP), ionized calcium (which is necessary for several steps of the coagulation cascade), and serotonin. Dense granules are similar to lysosomes with an acidic pH and even some lysosomal proteins like CD63. There is a granular adenine nucleotide pool within the dense granule. It is thought that it is made up of system of insoluble calcium. This pool is likely to be different than that of the cytoplasmic nucleotides. In some animals it has been shown that the platelets contain histamine. During exocytosis, the pool of ATP within the dense granule is released. Serotonin is picked up by the dense granules where it interacts with ATP and calcium. The serotonin that is then released by the dense granule, recruits other platelets and helps play a major role in stoping the loss of blood at the injury. The calcium from a dense granule accounts for the majority of the calcium within the platelets and plays a role in the binding of different proteins.
A deficiency of CD63 can be associated with Hermansky–Pudlak syndrome. The patients with this disease show signs of abnormal dense granules and melanosomes which can cause prolonged bleeding and albinism. Chediak-Higashi syndrome is an autosomal recessive disorder where patients platelets are have a deficient amount of dense granules. CHS is very similar to beige mouse.
The dense granule is very important in the coagulation cascade because of the bleeding disorders caused by a dense granule deficiency. However, the exact details of how it created is unknown. It has been observed that they are produced in bone marrow by megakaryocytes. Within the megakaryocytes it is thought that their production has something to do with the endocytotic pathway. Dense granules have their components sent to maturing dense granules using vesicular nucleotide transporters. This is what is thought to cause the build up of ADP/ATP in dense granules. This mechanism is also responsible for the build up of MRP4 which picks up cAMP for the dense granule. Mice with MRP4-/- will have dysfunctional platelets from cAMP not being takin up from the cytosol and placed into the dense granule.
There are a number of proteins that are within the dense granule membrane. To maintain the low pH within the granule, there is a Hydrogen ion pumping ATPase. Ral has been found within the granule's membrane. There are several adhesive receptors that have luminal binding domains and are expressed post exocytosis. These adhesive receptors help the adhesive receptors on the surface of the platelets. One of these receptors is GPIb. GPIb is one of the more important receptors within platelets.
The true function of a dense granule is still unknown. However, the secretion of dense granules occurs along with platelet activation. Both, ADP and collagen can cause the secretion of dense granules. Patients and mice with dense granule deficiency have a harder time forming a hemostatic plug and therefore have a longer bleed time.
The dense granules' matrix is dense with electrons that allow them to be detected through whole mount electron microscopy. The calcium levels within the dense granule allows for no extra staining when viewing the dense granule with an electron microscope. When observed by using transmission electron microscopy (TEM), these granules are osmophilic. The secretion of dense granules can be detected by seeing how much ATP/ADP is being released with luciferase-based luminescence. The relationship to ATP/ADP released can be used to then determine the secretion of dense granules. Another option is to observe the amount of serotonin being released from a platelet with a large amount of serotonin already on it. Another way to detect the secretion of dense granules is through flow cytometry. Since dense granules have surface membrane proteins, the activation of CD63 and LAMP-2 can be observed with flow cytometry.
- Michelson, A. D. (2013). Platelets (Vol. 3rd ed). Amsterdam: Academic Press. Retrieved from http://search.ebscohost.com.libproxy.clemson.edu/login.aspx?direct=true&db=e000xna&AN=485886
- Ambrosio, A. L., Boyle, J. A., & Di Pietro, S. M. (2012). Mechanism of platelet dense granule biogenesis: study of cargo transport and function of Rab32 and Rab38 in a model system. Blood, 120(19), 4072–4081. doi:10.1182/blood-2012-04-420745
- McNicol, A., & Israels, S. J. (1999). Platelet dense granules: Structure, function and implications for haemostasis doi://doi.org/10.1016/S0049-3848(99)00015-8 "
- James Joseph Marr; Timothy W. Nilsen; Richard Komuniecki (2003). Molecular medical parasitology. Academic Press. pp. 254–. ISBN 978-0-12-473346-6. Retrieved 12 November 2010.
- Díaz-Martín, R.D., Mercier, C., Gómez de León, C.T. et al. Parasitol Res (2019). https://doi.org/10.1007/s00436-019-06298-7
- Stuart H. Orkin; David G. Nathan; David Ginsburg; A. Thomas Look (2009). Nathan and Oski's hematology of infancy and childhood. Elsevier Health Sciences. pp. 1386–. ISBN 978-1-4160-3430-8. Retrieved 2 November 2010.
- Sharda, A., & Flaumenhaft, R. (2018). The life cycle of platelet granules. F1000Research, 7, 236. doi:10.12688/f1000research.13283.1
- Nishibori M, Cham B, McNicol A, Shalev A, Jain N, Gerrard J (1993). "The protein CD63 is in platelet dense granules, is deficient in a patient with Hermansky-Pudlak syndrome, and appears identical to granulophysin". J Clin Invest. 91 (4): 1775–82. doi:10.1172/JCI116388. PMC 288158. PMID 7682577.
|This cell biology article is a stub. You can help Wikipedia by expanding it.|