{"created":"2020-08-30T20:01:00.644840+00:00","id":3132,"links":{},"metadata":{"_buckets":{"deposit":"f95c92b6-93b0-4ef5-a6eb-52144efb5760"},"_deposit":{"id":"3132","owners":[],"pid":{"revision_id":0,"type":"recid","value":"3132"},"status":"published"},"_oai":{"id":"oai:meral.edu.mm:recid/3132","sets":["1582963366982:1597649530495"]},"communities":["um1"],"item_1583103067471":{"attribute_name":"Title","attribute_value_mlt":[{"subitem_1551255647225":"Expression of ACYL-Coenzyme A:Cholesterol Acyltransferase-1 (ACAT-1) Protein in Human Atherosclerotic Lesions and Cultured Monocytes-Macrophages","subitem_1551255648112":""}]},"item_1583103085720":{"attribute_name":"Description","attribute_value_mlt":[{"interim":"

The ACAT gene was first cloned in 1993 (Chang et al., J. Biol. Chem. 1993;268:20747-20755; designated as ACAT-1). Using affinity purified antibodies raised against N-terminal portion of human ACAT-1 protein, we performed immunohistochemical localization studies, and showed that the ACAT-1 protein was highly expressed in the atherosclerotic lesions of human aorta. We also performed cell-specific localization studies using double immunostaining, and showed that ACAT-1 was predominantly expressed in macrophages, but not in smooth muscle cells. We then used cell culture system in vitro to monitor the ACAT-1 expression in differentiating monocytes-macrophages

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