Loss of functional ELOVL4 depletes very long-chain fatty acids (> or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death. Export

@article{citeulike:2906289, abstract = {Mutations in elongation of very long-chain fatty acid-4 (ELOVL4) are associated with autosomal dominant Stargardt-like macular degeneration (STGD3), with a five base-pair (5 bp) deletion mutation resulting in the loss of 51 carboxy-terminal amino acids and truncation of the protein. In addition to the retina, Elovl4 is expressed in a limited number of mammalian tissues, including skin, with unknown function(s). We generated a knock-in mouse model with the 5-bp deletion in the Elovl4 gene. As anticipated, mice carrying this mutation in the heterozygous state (Elovl4(+/del)) exhibit progressive photoreceptor degeneration. Unexpectedly, homozygous mice (Elovl4(del/del)) display scaly, wrinkled skin, have severely compromised epidermal permeability barrier function, and die within a few hours after birth. Histopathological evaluation of the Elovl4(del/del) pups revealed no apparent abnormality(ies) in vital internal organs. However, skin histology showed an abnormally-compacted outer epidermis [stratum corneum (SC)], while electron microscopy revealed deficient epidermal lamellar body contents, and lack of normal SC lamellar membranes that are essential for permeability barrier function. Lipid analyses of epidermis from Elovl4(del/del) mice revealed a global decrease in very long-chain fatty acids (VLFAs) (i.e., carbon chain > or =C28) in both the ceramide/glucosylceramide and the free fatty-acid fractions. Strikingly, Elovl4(del/del) skin was devoid of the epidermal-unique omega-O-acylceramides, that are key hydrophobic components of the extracellular lamellar membranes in mammalian SC. These findings demonstrate that ELOVL4 is required for generating VLFA critical for epidermal barrier function, and that the lack of epidermal omega-O-acylceramides is incompatible with survival in a desiccating environment.}, address = {Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48105, USA.}, author = {Vasireddy, V. and Uchida, Y. and Salem, N. and Kim, S. Y. and Mandal, M. N. and Reddy, G. B. and Bodepudi, R. and Alderson, N. L. and Brown, J. C. and Hama, H. and Dlugosz, A. and Elias, P. M. and Holleran, W. M. and Ayyagari, R.}, citeulike-article-id = {2906289}, citeulike-linkout-0 = {http://view.ncbi.nlm.nih.gov/pubmed/17208947}, citeulike-linkout-1 = {http://www.hubmed.org/display.cgi?uids=17208947}, day = {1}, issn = {0964-6906}, journal = {Human molecular genetics}, keywords = {elovl4}, month = {March}, number = {5}, pages = {471--482}, posted-at = {2008-06-18 23:16:59}, priority = {2}, title = {Loss of functional ELOVL4 depletes very long-chain fatty acids (> or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/17208947}, volume = {16}, year = {2007} }

TY - JOUR ID - citeulike:2906289 L3 - citeulike-article-id:2906289 N2 - Mutations in elongation of very long-chain fatty acid-4 (ELOVL4) are associated with autosomal dominant Stargardt-like macular degeneration (STGD3), with a five base-pair (5 bp) deletion mutation resulting in the loss of 51 carboxy-terminal amino acids and truncation of the protein. In addition to the retina, Elovl4 is expressed in a limited number of mammalian tissues, including skin, with unknown function(s). We generated a knock-in mouse model with the 5-bp deletion in the Elovl4 gene. As anticipated, mice carrying this mutation in the heterozygous state (Elovl4(+/del)) exhibit progressive photoreceptor degeneration. Unexpectedly, homozygous mice (Elovl4(del/del)) display scaly, wrinkled skin, have severely compromised epidermal permeability barrier function, and die within a few hours after birth. Histopathological evaluation of the Elovl4(del/del) pups revealed no apparent abnormality(ies) in vital internal organs. However, skin histology showed an abnormally-compacted outer epidermis [stratum corneum (SC)], while electron microscopy revealed deficient epidermal lamellar body contents, and lack of normal SC lamellar membranes that are essential for permeability barrier function. Lipid analyses of epidermis from Elovl4(del/del) mice revealed a global decrease in very long-chain fatty acids (VLFAs) (i.e., carbon chain > or =C28) in both the ceramide/glucosylceramide and the free fatty-acid fractions. Strikingly, Elovl4(del/del) skin was devoid of the epidermal-unique omega-O-acylceramides, that are key hydrophobic components of the extracellular lamellar membranes in mammalian SC. These findings demonstrate that ELOVL4 is required for generating VLFA critical for epidermal barrier function, and that the lack of epidermal omega-O-acylceramides is incompatible with survival in a desiccating environment. IS - 5 JF - Human molecular genetics SN - 0964-6906 AD - Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48105, USA. EP - 482 TI - Loss of functional ELOVL4 depletes very long-chain fatty acids (> or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death. VL - 16 SP - 471 KW - elovl4 AU - Vasireddy, V AU - Uchida, Y AU - Salem, N AU - Kim, SY AU - Mandal, MN AU - Reddy, GB AU - Bodepudi, R AU - Alderson, NL AU - Brown, JC AU - Hama, H AU - Dlugosz, A AU - Elias, PM AU - Holleran, WM AU - Ayyagari, R PY - 2007/03/01/ UR - http://view.ncbi.nlm.nih.gov/pubmed/17208947 ER -