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The role of multivesicular endosomes and OA1 in melanosome biogenesis

Reference	BB/D011841/1
Principal Investigator / Supervisor	Professor Clare Futter
Co-Investigators / Co-Supervisors
Institution	University College London
Department	Institute of Ophthalmology
Funding type	Research
Value (£)	218,064
Status	Completed
Type	Research Grant
Start date	11/09/2006
End date	10/09/2009
Duration	36 months

Abstract

The overall objectives of this project are 1. to determine the role of multivesicular endosome/body (MVB) formation and inward vesiculation within MVB in melanosome biogenesis and 2. to determine whether OA1 regulates MVB formation, function or fate in melanogenic cells. The origin of melanosomes within melanocytes and retinal pigment epithelial (RPE) cells has been controversial but there is considerable evidence that MVBs lie on the pathway leading to the melanosome. One of the most compelling pieces of evidence for a role for the MVB in initiating melanosome biogenesis is that pmel17, a protein required for the generation of striations upon which melanin is deposited, is found on the internal vesicles of multivesicular vacuoles in melanogenic cells and, when exogenously expressed in non melanogenic cells, localises to MVBs where it induces striations at high levels of expression. We have shown in non melanogenic cells that there is more than one population of MVBs. We will determine which populations of MVB lie on the melanosomal pathway by i) expressing pmel17 in non-melanogenic cells and comparing its distribution to that of previously characterised markers of MVB subpopulations ii) determining the effects of pmel17 expression on MVB formation and inward vesiculation in non-melanogenic cells and iii) determining whether pmel17 is localised to a subset of MVBs in melanogenic cells. The melanogenic cell lines examined will be immortalised skin melanocytes and immortalised retinal pigment epithelial cell lines. Proteins will be localised by a combination of immunofluorescence and cry-immuno electron microscopy (EM). MVB formation and inward vesiculation within MVB will be measured by conventional EM using quantitative assays we have developed for measuring these processes, where an MVB is defined as a vacuole with a diameter of greater than 200nm and one or more internal vesicles. We will then determine the role of components of the core machinery required for MVB formation and inward vesiculation on the initiation of melanosome biogenesis and melanosome maturation. Cells will be depleted of Tsg101, Hrs or annexin 1 using siRNA or will be micro-injected with inhibitory anti-Vps34 antibody. The effects of these treatments on formation of pmel17-containing MVBs, inward vesiculation within them, sorting of pmel17 onto internal vesicles and striation formation in non-melanogenic cells exogenously expressing pmel17 will be determined. Melanogenic cells will then be used to determine the effects of these treatments on melanosome formation. To examine the role of OA1 within the MVB we will first determine to which population of MVBs OA1 is localised in non-melanogenic and melanogenic cells. The effects of OA1 expression on MVB formation and inward vesiculation and on the sorting of pmel17 and striation formation in non-melanogenic cells will then be determined as described for pmel17 above. Finally we determine the effects of siRNA-mediated depletion of OA1 on melanosome formation in melanogenic cells. Together these studies will address the mechanisms regulating the formation of an organelle that forms the body's natural defence against ultraviolet irradiation and will aid our understanding of how these mechanisms are compromised in human diseases, including ocular albinism.

Summary

One of the main functions of melanin pigment in the skin is to act as a sunscreen to absorb ultraviolet radiation and prevent DNA damage and skin cancer. Melanin is synthesised and stored in membrane bound organelles called melanosomes. Melanosomes are found in melanocytes of the skin and also in cells of the eye, including in retinal pigment epithelial (RPE) cells. RPE cells lie immediately beneath the rods and cones (the cells of the eye that detect and transduce light). Deficit of melanin pigment, as is found in the various types of albinism, leads to severe visual impairment. Some types of albinsm are caused by defects in the ability to synthesise melanin while others are caused by defects in the ability to make melanosomes. The mechanisms whereby melanosomes are formed are not fully characterised but they involve the endocytic pathway, which is the route where by extracellular molecules like viruses and nutrients are taken up into the cell. Extracellular molecules are delivered to endosomes where they meet proteins that have been newly synthesised by the cell. From the endosome proteins may be delivered to many different places, such as the lysosome for degradation or back to the cell surface. We have shown that this critical decision is taken in multivesicular endosomes/bodies (MVB). Proteins that are to be delivered to the lysosome for degradation are sorted onto the internal vesicles of MVB while proteins that are to be returned to the plasma membrane stay on the perimeter membrane of the MVB. In melanin synthesising cells the MVB may also be involved in delivering melanosomal proteins to the melanosome or a subpopulation of MVBs may develop into melanosomes. In melanin producing cells a protein called pmel 17 is required for the generation of internal striations within the forming melanosome upon which melanin is deposited. In the very early stages of melanosome formation pmel17 is found on the internal vesicles of MVBs and when sufficient protein has accumulated on the internal vesicles of MVB striations begin to form. Striations will even begin to form within the MVBs of cells which do not normally make melanin if they are genetically modified so that they make pmel17. This implies that inward vesiculation within MVB may play a critical role in formation of internal striations and in melanosome biogenesis. Recently components of the molecular machinery that are involved in sorting of proteins within MVB and in MVB formation have been identified. We have been determining the function of some of these proteins using electron microscopy (EM), as EM is the only way to visualise the very small (50nm diameter) internal vesicles of MVB. So far we have determined the functions of some of these proteins in cells which do not make melanosomes. We now propose to determine the role of these proteins in the formation of melanosomes in melanocytes and RPE cells. In addition to determining the role of the core components of the MVB machinery we will determine the role of a protein that is only expressed in cells that make melanosomes. OA1 is the protein which is defective in the most common type of ocular albinism and patients with this disease can make melanin but make a reduced number of unusually large melanosomes. This protein has been found associated with MVBs and has been proposed to play a role at the level of the MVB in melanosome formation. We will use our EM assays to determine what OA1 does within the MVB. Together these studies will elucidate the fundamental mechanisms regulating the formation of an organelle which is the body's natural defence mechanism against the effects of the sun and which also plays an important role in vision. This will help us to understand how these mechanisms fail in human disease.

Committee	Closed Committee - Biochemistry & Cell Biology (BCB)
Research Topics	X – not assigned to a current Research Topic
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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