1971
DOI: 10.1007/bf00277378
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Electron microscopy of lipofuscin pigment stained by the schm�rl and fontana techniques

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1977
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Cited by 5 publications
(2 citation statements)
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“…Furthermore, glycogens were mainly localized in GLAST+ astrocytes and their progenitor cells ( S3A Fig ), while they were much less localized in the PDGFRα+ OPCs or excluded from Iba1+ microglia ( S3B–S3D Fig ). Microglia somas were identified using established criteria, including lysosomes, lipofuscin, and a long ER ( Fig 1D ) [ 19 , 30 , 31 ]. Fig 1 also shows a unique cell that contains relatively sparse cytoplasmic organelles and few or no glycogen granules, but no intermediate filaments (cell C in Fig 1 , S1 and S2 Figs).…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, glycogens were mainly localized in GLAST+ astrocytes and their progenitor cells ( S3A Fig ), while they were much less localized in the PDGFRα+ OPCs or excluded from Iba1+ microglia ( S3B–S3D Fig ). Microglia somas were identified using established criteria, including lysosomes, lipofuscin, and a long ER ( Fig 1D ) [ 19 , 30 , 31 ]. Fig 1 also shows a unique cell that contains relatively sparse cytoplasmic organelles and few or no glycogen granules, but no intermediate filaments (cell C in Fig 1 , S1 and S2 Figs).…”
Section: Resultsmentioning
confidence: 99%
“…It is generally agreed that its formation involves oxidation of lipids, and that it develops in lesions where unsaturated fatty acids accumulate in abnormal torm and amoutit (Hartroft & Porta 1965). Seveial investigators have suggested that ceroid arises through the breakdown of damaged otganclles and membranes by lysosotnes which arc unable to digest the material completely (Hendy 1971). Hess (1955) proposed a tnitochondrial origin based on electron microscopic observations.…”
Section: Discussionmentioning
confidence: 99%