skip to main content


Title: Chip-to-chip Optical Data Communications using Polarization Division Multiplexing
Award ID(s):
1763503
NSF-PAR ID:
10283230
Author(s) / Creator(s):
; ; ; ; ;
Date Published:
Journal Name:
Proc. of IEEE High-Performance Extreme Computing Conference
Page Range / eLocation ID:
1 to 8
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Endothelial mechanobiology is a key consideration in the progression of vascular dysfunction, including atherosclerosis. However mechanistic connections between the clinically associated physical stimuli, vessel stiffness and shear stress, and how they interact to modulate plaque progression remain incompletely characterized. Vessel-chip systems are excellent candidates for modeling vascular mechanobiology as they may be engineered from the ground up, guided by the mechanical parameters present in human arteries and veins, to recapitulate key features of the vasculature. Here, we report extensive validation of a vessel-chip model of endothelial yes-associated protein (YAP) mechanobiology, a protein sensitive to both matrix stiffness and shearing forces and, importantly, implicated in atherosclerotic progression. Our model captures the established endothelial mechanoresponse, with endothelial alignment, elongation, reduction of adhesion molecules, and YAP cytoplasmic retention under high laminar shear. Conversely, we observed disturbed morphology, inflammation, and nuclear partitioning under low, high, and high oscillatory shear. Examining targets of YAP transcriptional co-activation, connective tissue growth factor (CTGF) is strongly downregulated by high laminar shear, whereas it is strongly upregulated by low shear or oscillatory flow. Ankyrin repeat domain 1 (ANKRD1) is only upregulated by high oscillatory shear. Verteporfin inhibition of YAP reduced the expression of CTGF but did not affect ANKRD1. Lastly, substrate stiffness modulated the endothelial shear mechanoresponse. Under high shear, softer substrates showed the lowest nuclear localization of YAP whereas stiffer substrates increased nuclear localization. Low shear strongly increased nuclear localization of YAP across stiffnesses. Together, we have validated a model of endothelial mechanobiology and describe a clinically relevant biological connection between matrix stiffness, shear stress, and endothelial activation via YAP mechanobiology. 
    more » « less
  2. Emerging embedded systems, such as autonomous robots/vehicles, demand a new system-on-a-chip (SoC) that is ultra-low power (mW or even sub-mW level) but highly robust. Such an SoC typically integrates heterogeneous building blocks for supporting a range of features, each ideally operating in an independent voltage and frequency (V/F) domain [1]. In such an architecture, a network-on-chip (NoC) has played a key role to enable high-speed and energy-efficient networking. However, it is increasingly challenging to meet a robustness target since each V/F domain uses a significantly different voltage, e.g., from nominal 1V to near-threshold voltage (NTV), and clock frequency, e.g., from hundreds of MHz to sub-MHz. Furthermore, any two clocks may have uncertain and time-varying phase and frequency relationships. These properties significantly worsen robustness, particularly metastability, in an NoC. 
    more » « less
  3. null (Ed.)