Other Publications (1)
Articles by David R. Myers in JoVE
Hematologic 질환의 Microvascular 상호 작용 유학을위한 Endothelialized Microfluidics David R. Myers*1,2,3,4, Yumiko Sakurai*1,2,3,4, Reginald Tran1,2,3,4, Byungwook Ahn1,2,3,4, Elaissa Trybus Hardy1,2,3,4, Robert Mannino1,2,3,4, Ashley Kita1,2,3,4, Michelle Tsai1,2,3,4, Wilbur A. Lam1,2,3,4 1Department of Pediatrics, Emory University School of Medicine, 2Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 3Aflac Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta, 4Winship Cancer Institute of Emory University microvascular 크기의 채널 (<30 μm의)와 microfluidic 장치의 전체 내부 3D 표면에 걸쳐 문화 내피 세포 단일층를하는 방법이 설명되어 있습니다. 이
Other articles by David R. Myers on PubMed
Microenvironmental Geometry Guides Platelet Adhesion and Spreading: a Quantitative Analysis at the Single Cell Level PloS One. 2011 | Pubmed ID: 22028878 To activate clot formation and maintain hemostasis, platelets adhere and spread onto sites of vascular injury. Although this process is well-characterized biochemically, how the physical and spatial cues in the microenvironment affect platelet adhesion and spreading remain unclear. In this study, we applied deep UV photolithography and protein micro/nanostamping to quantitatively investigate and characterize the spatial guidance of platelet spreading at the single cell level and with nanoscale resolution. Platelets adhered to and spread only onto micropatterned collagen or fibrinogen surfaces and followed the microenvironmental geometry with high fidelity and with single micron precision. Using micropatterned lines of different widths, we determined that platelets are able to conform to micropatterned stripes as thin as 0.6 µm and adopt a maximum aspect ratio of 19 on those protein patterns. Interestingly, platelets were also able to span and spread over non-patterned regions of up to 5 µm, a length consistent with that of maximally extended filopodia. This process appears to be mediated by platelet filopodia that are sensitive to spatial cues. Finally, we observed that microenvironmental geometry directly affects platelet biology, such as the spatial organization and distribution of the platelet actin cytoskeleton. Our data demonstrate that platelet spreading is a finely-tuned and spatially-guided process in which spatial cues directly influence the biological aspects of how clot formation is regulated.