Bui Tam V, Han Yun, Radu Roxana A, Travis Gabriel H, Mata Nathan L
Sytera, Inc., 505 Coast Boulevard South, La Jolla, CA 92037, USA.
J Biol Chem. 2006 Jun 30;281(26):18112-9. doi: 10.1074/jbc.M601380200. Epub 2006 Apr 25.
Mutations in the photoreceptor-specific ABCA4 gene are associated with several inherited retinal and macular degenerations. A prominent phenotype of these diseases is the accumulation of cytotoxic lipofuscin fluorophores such as A2E within the retinal pigment epithelium. Another compound, dihydro-N-retinylidene-N-retinylphosphatidyl-ethanolamine (A2PE-H(2)), also accumulates in retinas of mice and humans harboring ABCA4 mutations and was proposed to be a precursor of A2E. The role of A2PE-H(2) in the biogenesis of A2E and its relationship to other retinal fluorophores has not been previously investigated. We report spectral properties and structural relationships of the principal retinal fluorophores that accumulate in retina and retinal pigment epithelium of abca4(-/-) mice. A long wavelength fluorescence emission intrinsic to abca4(-/-) retinal explants is shown to emanate from A2PE-H(2). All-trans retinal dimer conjugates, which were also identified in the retinal explants, possessed distinct fluorescence and structural properties and, unlike A2PE-H(2), did not accumulate in an age-dependent manner. Derivative absorbance and fluorescence spectroscopy revealed that A2PE-H(2), A2E, and N-retinylidene-N-retinyl-phosphatidylethanolamine (A2PE), a known precursor of A2E, share common electronic and resonant structures. Importantly, collision-induced dissociation of A2PE-H(2) produced daughter ions that were identical to authentic A2E and its daughter ions. Finally, intravitreal administration of A2PE-H(2) to wild-type mice resulted in the formation of A2PE and A2E. These data validate a previously hypothesized biosynthetic pathway for A2E and implicate A2PE-H(2) as a precursor in this pathway. Fluorescence properties of A2PE-H(2) and other related fluorophores characterized in this report have significance for evaluation of human retinal diseases characterized by aberrant fundus autofluorescence.
感光细胞特异性ABCA4基因的突变与多种遗传性视网膜和黄斑变性相关。这些疾病的一个显著表型是细胞毒性脂褐素荧光团如A2E在视网膜色素上皮内积累。另一种化合物二氢-N-视黄叉基-N-视黄基磷脂酰乙醇胺(A2PE-H₂)也在携带ABCA4突变的小鼠和人类视网膜中积累,并被认为是A2E的前体。此前尚未研究A2PE-H₂在A2E生物合成中的作用及其与其他视网膜荧光团的关系。我们报告了在abca4(-/-)小鼠的视网膜和视网膜色素上皮中积累的主要视网膜荧光团的光谱特性和结构关系。研究表明,abca4(-/-)视网膜外植体特有的长波长荧光发射源自A2PE-H₂。在视网膜外植体中也鉴定出的全反式视黄醛二聚体共轭物具有独特的荧光和结构特性,与A2PE-H₂不同,它们不会以年龄依赖的方式积累。衍生吸收光谱和荧光光谱显示,A2PE-H₂、A2E和A2E的已知前体N-视黄叉基-N-视黄基磷脂酰乙醇胺(A2PE)具有共同的电子和共振结构。重要的是,A2PE-H₂的碰撞诱导解离产生的子离子与真实的A2E及其子离子相同。最后,向野生型小鼠玻璃体内注射A2PE-H₂导致了A2PE和A2E的形成。这些数据验证了先前假设的A2E生物合成途径,并表明A2PE-H₂是该途径中的前体。本报告中表征的A2PE-H₂和其他相关荧光团的荧光特性对于评估以异常眼底自发荧光为特征的人类视网膜疾病具有重要意义。