Alport syndrome pathophysiology: Difference between revisions
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==Pathogenesis== | ==Pathogenesis== | ||
Alport Syndrome occurs because of mutation involving the alpha-3, alpha-4, and the alpha-5 chains. These chains are essential in forming the basement membrane. The mutations of these chains are caused by a gene mutation in COL4A5 that encodes the alpha-5 chain on the X-chromosome . A gene mutation of COL4A3 that encodes the alpha-3 chain and COL4A4 that affects the alpha-4 chain. The genes COL4A3 or COL4A4 are essential for encoding for nephrin, podocin, and CD2-associated protein. <ref name="pmid128151412">{{cite journal| author=Hudson BG, Tryggvason K, Sundaramoorthy M, Neilson EG| title=Alport's syndrome, Goodpasture's syndrome, and type IV collagen. | journal=N Engl J Med | year= 2003 | volume= 348 | issue= 25 | pages= 2543-56 | pmid=12815141 | doi=10.1056/NEJMra022296 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12815141 }}</ref> | |||
A mutation is any of these genes causes the polypeptides to be misfolded and the proteins to be improperly assembled. This is do to mRNA not being read correctly by the ribosomes. This causes alpha-3, alpha-4, and alpha-5 chains to be shutdown. Which in turn shuts down the normal processes of gene development in the glomerular basement membrane. This allows embryonic developmental chains alpha-1.alpha-1.alpha-2. to be produced in the glomerular basement membrane. By only having the embryonic developmental chains produced in the glomerular basement membrane, the glomerular basement membrane is not able to be formed properly. This process inhibits the glomerular basement membrane from becoming mature and allows for the basement membrane to become more prone as it allows for endoproteolysis, the break down of protein structure. It also leaves the glomerular basement membrane to become more prone to oxidative stressors, as alpha-1.alpha-1.alpha-2. are not as protective as alpha-3, alpha-4, and alpha-5 chains. | |||
As time progresses, oxidative stressors and endoproteolysis cause the glomerular basement membrane to become unevenly thicken, split and unfortunately damaged in a way that the renals are no longer able to function properly.<ref name="pmid12815141">{{cite journal| author=Hudson BG, Tryggvason K, Sundaramoorthy M, Neilson EG| title=Alport's syndrome, Goodpasture's syndrome, and type IV collagen. | journal=N Engl J Med | year= 2003 | volume= 348 | issue= 25 | pages= 2543-56 | pmid=12815141 | doi=10.1056/NEJMra022296 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12815141 }}</ref> | |||
==Genetics== | ==Genetics== | ||
Revision as of 15:17, 2 November 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]
Overview
Pathogenesis
Alport Syndrome occurs because of mutation involving the alpha-3, alpha-4, and the alpha-5 chains. These chains are essential in forming the basement membrane. The mutations of these chains are caused by a gene mutation in COL4A5 that encodes the alpha-5 chain on the X-chromosome . A gene mutation of COL4A3 that encodes the alpha-3 chain and COL4A4 that affects the alpha-4 chain. The genes COL4A3 or COL4A4 are essential for encoding for nephrin, podocin, and CD2-associated protein. [1]
A mutation is any of these genes causes the polypeptides to be misfolded and the proteins to be improperly assembled. This is do to mRNA not being read correctly by the ribosomes. This causes alpha-3, alpha-4, and alpha-5 chains to be shutdown. Which in turn shuts down the normal processes of gene development in the glomerular basement membrane. This allows embryonic developmental chains alpha-1.alpha-1.alpha-2. to be produced in the glomerular basement membrane. By only having the embryonic developmental chains produced in the glomerular basement membrane, the glomerular basement membrane is not able to be formed properly. This process inhibits the glomerular basement membrane from becoming mature and allows for the basement membrane to become more prone as it allows for endoproteolysis, the break down of protein structure. It also leaves the glomerular basement membrane to become more prone to oxidative stressors, as alpha-1.alpha-1.alpha-2. are not as protective as alpha-3, alpha-4, and alpha-5 chains.
As time progresses, oxidative stressors and endoproteolysis cause the glomerular basement membrane to become unevenly thicken, split and unfortunately damaged in a way that the renals are no longer able to function properly.[2]
Genetics
Alport syndrome is a rare inherited disease, that is passed down by the mother's or father's X chromosome or a mutation involving chromosome 2. There are three forms of inheritance. It can either be x-linked, autosomal dominant, and autosomal recessive.[3]
Gross Pathology
Microscopic Pathology
Alport’s syndrome is characterized by the defect of alpha chains of type IV collagen that constitute a triad of manifestations: renal, auditory, and ocular. Involvement of the glomerular basement membrane is the hallmark of Alport’s syndrome.[4][5] It is still controversial as to whether the basement membrane becomes thicker or thinner to induce splitting.
| Manifestations | Renal | Auditory | Ocular |
| Molecular Findings | Absence of collagen network of the glomerular basement membrane (GBM) that is normally formed by podocytes and endothelial cells[6][7][8] | Cellular loss, including hair cells of Corti, and edema associated with atrophy of tissue[9][10][11][12] | Cellular loss and mitochondrial edema. Honeycombing of broken abnormal filaments that are surrounded by vacuolated spheres and membranes[13][10] |
| Histopathological Changes | Lamellated GBM and splitting with appearance of false layers of the basement membrane leading to focal sclerosis of glomeruli[9][10][11][4] | Basement changes of the stria vascularis of the cochlea | Pathological changes involving the lens capsule, the largest basement membrane in the eye[13][10] |
Alpha chains of type IV collagen are located at specific regions in the body. However, the involvement of one type of alpha chain does not necessarily have to involve all corresponding beds that are known to be composed of that same collagen type. To date, there has been no valid hypothesis of why renal, auditory, and ocular manifestations are observed in Alport’s syndrome, but other basement membrane beds involving alpha-5 type IV collagen are no involved, such as the epidermal basement membrane of the skin.[10][14]
References
- ↑ Hudson BG, Tryggvason K, Sundaramoorthy M, Neilson EG (2003). "Alport's syndrome, Goodpasture's syndrome, and type IV collagen". N Engl J Med. 348 (25): 2543–56. doi:10.1056/NEJMra022296. PMID 12815141.
- ↑ Hudson BG, Tryggvason K, Sundaramoorthy M, Neilson EG (2003). "Alport's syndrome, Goodpasture's syndrome, and type IV collagen". N Engl J Med. 348 (25): 2543–56. doi:10.1056/NEJMra022296. PMID 12815141.
- ↑ Savige J, Gregory M, Gross O, Kashtan C, Ding J, Flinter F (2013). "Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy". J Am Soc Nephrol. 24 (3): 364–75. doi:10.1681/ASN.2012020148. PMID 23349312.
- ↑ 4.0 4.1 Bodziak KA, Hammond WS, Molitoris BA (1994). "Inherited diseases of the glomerular basement membrane". Am J Kidney Dis. 23 (4): 605–18. PMID 8154501.
- ↑ Kashtan CE, Michael AF (1993). "Alport syndrome: from bedside to genome to bedside". Am J Kidney Dis. 22 (5): 627–40. PMID 8238007.
- ↑ Abrahamson DR, Hudson BG, Stroganova L, Borza DB, St John PL (2009). "Cellular origins of type IV collagen networks in developing glomeruli". J Am Soc Nephrol. 20 (7): 1471–9. doi:10 .1681/ASN.2008101086 Check
|doi=value (help). PMC 2709682. PMID 19423686. - ↑ Miner JH (1998). "Developmental biology of glomerular basement membrane components". Curr Opin Nephrol Hypertens. 7 (1): 13–9. PMID 9442357.
- ↑ St John PL, Abrahamson DR (2001). "Glomerular endothelial cells and podocytes jointly synthesize laminin-1 and -11 chains". Kidney Int. 60 (3): 1037–46. doi:10.1046/j.1523-1755.2001.0600031037.x. PMID 11532098.
- ↑ 9.0 9.1 Chugh KS, Sakhuja V, Agarwal A, Jha V, Joshi K, Datta BN; et al. (1993). "Hereditary nephritis (Alport's syndrome)--clinical profile and inheritance in 28 kindreds". Nephrol Dial Transplant. 8 (8): 690–5. PMID 8414153.
- ↑ 10.0 10.1 10.2 10.3 10.4 McCarthy PA, Maino DM (2000). "Alport syndrome: a review". Clin Eye Vis Care. 12 (3–4): 139–150. PMID 11137428.
- ↑ 11.0 11.1 Andreoli SP, Deaton M (1992). "Alport's syndrome". Ear Nose Throat J. 71 (10): 508–11. PMID 1425373.
- ↑ Grondalski SJ, Bennett GR (1989). "Alport's syndrome: review and case report". Optom Vis Sci. 66 (6): 396–8. PMID 2771325.
- ↑ 13.0 13.1 Streeten BW, Robinson MR, Wallace R, Jones DB (1987). "Lens capsule abnormalities in Alport's syndrome". Arch Ophthalmol. 105 (12): 1693–7. PMID 3689194.
- ↑ Barker DF, Hostikka SL, Zhou J, Chow LT, Oliphant AR, Gerken SC; et al. (1990). "Identification of mutations in the COL4A5 collagen gene in Alport syndrome". Science. 248 (4960): 1224–7. PMID 2349482.