<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>55</viewCount><searchCount>0</searchCount></scores><additional><submitter>Sulkin MS</submitter><funding>NHLBI NIH HHS</funding><pagination>55-60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4295200</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>188(1)</volume><pubmed_abstract>The ventricular human myocyte is spatially organized for optimal ATP and Ca(2+) delivery to sarcomeric myosin and ionic pumps during every excitation-contraction cycle. Comprehension of three-dimensional geometry of the tightly packed ultrastructure has been derived from discontinuous two-dimensional images, but has never been precisely reconstructed or analyzed in human myocardium. Using a focused ion beam scanning electron microscope, we created nanoscale resolution serial images to quantify the three-dimensional ultrastructure of a human left ventricular myocyte. Transverse tubules (t-tubule), lipid droplets, A-bands, and mitochondria occupy 1.8, 1.9, 10.8, and 27.9% of the myocyte volume, respectively. The complex t-tubule system has a small tortuosity (1.04±0.01), and is composed of long transverse segments with diameters of 317±24nm and short branches. Our data indicates that lipid droplets located well beneath the sarcolemma are proximal to t-tubules, where 59% (13 of 22) of lipid droplet centroids are within 0.50μm of a t-tubule. This spatial association could have an important implication in the development and treatment of heart failure because it connects two independently known pathophysiological alterations, a substrate switch from fatty acids to glucose and t-tubular derangement.</pubmed_abstract><journal>Journal of structural biology</journal><pubmed_title>Nanoscale three-dimensional imaging of the human myocyte.</pubmed_title><pmcid>PMC4295200</pmcid><funding_grant_id>F30 HL114310</funding_grant_id><funding_grant_id>R01 HL114395</funding_grant_id><pubmed_authors>Van Leer B</pubmed_authors><pubmed_authors>Holzem KM</pubmed_authors><pubmed_authors>Efimov IR</pubmed_authors><pubmed_authors>Sulkin MS</pubmed_authors><pubmed_authors>Bugge C</pubmed_authors><pubmed_authors>Laughner JI</pubmed_authors><pubmed_authors>Yang F</pubmed_authors><pubmed_authors>Green K</pubmed_authors><view_count>55</view_count></additional><is_claimable>false</is_claimable><name>Nanoscale three-dimensional imaging of the human myocyte.</name><description>The ventricular human myocyte is spatially organized for optimal ATP and Ca(2+) delivery to sarcomeric myosin and ionic pumps during every excitation-contraction cycle. Comprehension of three-dimensional geometry of the tightly packed ultrastructure has been derived from discontinuous two-dimensional images, but has never been precisely reconstructed or analyzed in human myocardium. Using a focused ion beam scanning electron microscope, we created nanoscale resolution serial images to quantify the three-dimensional ultrastructure of a human left ventricular myocyte. Transverse tubules (t-tubule), lipid droplets, A-bands, and mitochondria occupy 1.8, 1.9, 10.8, and 27.9% of the myocyte volume, respectively. The complex t-tubule system has a small tortuosity (1.04±0.01), and is composed of long transverse segments with diameters of 317±24nm and short branches. Our data indicates that lipid droplets located well beneath the sarcolemma are proximal to t-tubules, where 59% (13 of 22) of lipid droplet centroids are within 0.50μm of a t-tubule. This spatial association could have an important implication in the development and treatment of heart failure because it connects two independently known pathophysiological alterations, a substrate switch from fatty acids to glucose and t-tubular derangement.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Oct</publication><modification>2024-11-08T14:10:07.456Z</modification><creation>2019-03-27T01:43:29Z</creation></dates><accession>S-EPMC4295200</accession><cross_references><pubmed>25160725</pubmed><doi>10.1016/j.jsb.2014.08.005</doi></cross_references></HashMap>