Department of Biochemistry and Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37240, United States.
Department of Ophthalmology and Visual Science, University of Alabama at Birmingham, Birmingham, AL 35294, United States.
J Am Soc Mass Spectrom. 2020 Dec 2;31(12):2426-2436. doi: 10.1021/jasms.0c00119. Epub 2020 Jul 24.
The human retina provides vision at light levels ranging from starlight to sunlight. Its supporting tissues regulate plasma-delivered lipophilic essentials for vision, including retinoids. The macula is an anatomic specialization for high-acuity and color vision that is also vulnerable to prevalent blinding diseases. The retina's exquisite architecture comprises numerous cell types that are aligned horizontally, yielding structurally distinct cell, synaptic, and vascular layers that are visible in histology and in diagnostic clinical imaging. MALDI imaging mass spectrometry (IMS) is now capable of uniting low micrometer spatial resolution with high levels of chemical specificity. In this study, a multimodal imaging approach fortified with accurate multi-image registration was used to localize lipids in human retina tissue at laminar, cellular, and subcellular levels. Multimodal imaging results indicate differences in distributions and abundances of lipid species across and within single cell types. Of note are distinct localizations of signals within specific layers of the macula. For example, phosphatidylethanolamine and phosphatidylinositol lipids were localized to central RPE cells, whereas specific plasmalogen lipids were localized to cells of the perifoveal RPE and Henle fiber layer. Subcellular compartments of photoreceptors were distinguished by PE(20:0_22:5) in the outer nuclear layer, PE(18:0_22:6) in outer and inner segments, and cardiolipin CL(70:5) in the mitochondria-rich inner segments. Several lipids, differing by a single double bond, have markedly different distributions between the central fovea and the ganglion cell and inner nuclear layers. A lipid atlas, initiated in this study, can serve as a reference database for future examination of diseased tissues.
人视网膜在从星光到阳光的光照水平下提供视觉。其支持组织调节为视觉提供的亲脂性必需物质,包括类视黄醇。黄斑是一种高敏度和色觉的解剖学特化区域,也容易受到流行的致盲性疾病的影响。视网膜的精致结构由众多水平排列的细胞类型组成,产生结构上不同的细胞、突触和血管层,在组织学和诊断临床成像中可见。基质辅助激光解吸电离成像质谱(MALDI IMS)现在能够将低微米级别的空间分辨率与高水平的化学特异性结合起来。在这项研究中,一种多模态成像方法,辅以精确的多图像配准,用于在层状、细胞和亚细胞水平定位人视网膜组织中的脂质。多模态成像结果表明,脂质种类在单个细胞类型内和之间的分布和丰度存在差异。值得注意的是,在黄斑的特定层内,信号的定位存在明显差异。例如,磷脂酰乙醇胺和磷脂酰肌醇脂质定位于中央 RPE 细胞,而特定的血浆脂质定位于周边部 RPE 和 Henle 纤维层的细胞。光感受器的亚细胞区室通过在外核层中的 PE(20:0_22:5)、在外节和内节中的 PE(18:0_22:6)以及在线粒体丰富的内节中的心磷脂 CL(70:5)来区分。几种脂质仅相差一个双键,在中央凹和节细胞和内核层之间的分布有明显差异。本研究中启动的脂质图谱可以作为未来研究疾病组织的参考数据库。