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Lab on a Chip

A compartmentalized microfluidic chip with crisscross microgrooves and electrophysiological electrodes for modeling the blood–retinal barrier

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* Corresponding authors

Institut de Microelectrònica de Barcelona, IMB-CNM (CSIC), 08193, Bellaterra, Barcelona, Spain Spring Court Carnage Military Boots outlet with credit card pre order cheap price where to buy cheap real rpTxiz59

CIBER-BBN, Networking Centre on Bioengineering, Biomaterials and Nanomedicine, Barcelona, Spain

Departamento de Microelectrónica y Sistemas Electrónicos, Universitat Autònoma de Barcelona, Spain

Diabetes and Metabolism Research Unit, Vall d'Hebron Research Institute, Barcelona, and CIBERDEM-Instituto de Salud Carlos III, Madrid, Spain

The interconnection of different tissue–tissue interfaces may extend organ-on-chips to a new generation of sophisticated models capable of recapitulating more complex organ-level functions. Single interfaces are largely recreated in organ-on-chips by culturing the cells on opposite sides of a porous membrane that splits a chamber in two or by connecting the cells of two adjacent compartments through microchannels. However, it is difficult to interconnect more than one interface using these approaches. To address this challenge, we present a novel microfluidic device where cells are arranged in parallel compartments and are highly interconnected through a grid of microgrooves, which facilitates paracrine signaling and heterotypic cell–cell contact between multiple tissues. In addition, the device includes electrodes on the substrate for the measurement of transepithelial electrical resistance (TEER). Unlike conventional methods for measuring the TEER where electrodes are on each side of the cell barrier, a method with only electrodes on the substrate has been validated. As a proof-of-concept, we have used the device to mimic the structure of the blood–retinal barrier by co-culturing primary human retinal endothelial cells (HREC), a human neuroblastoma cell line (SH-SY5Y), and a human retinal pigment epithelial cell line (ARPE-19). Cell barrier formations were assessed by a permeability assay, TEER measurements, and ZO-1 expression. These results validate the proposed microfluidic device with microgrooves as a promising tool for the compartmentalization and monitoring of barrier tissues.

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32 East 69th Street, November 2–December 23, 2017;opening reception, 6 p.m.–8 p.m.

Jessica Jackson Hutchins. Courtesy of Marianne Boesky Gallery.

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Look to the ceiling at Marianne Boesky Gallery, where Jessica Jackson Hutchins has installed some of her new experimental fused glass works as skylights. The pieces feature portraits of activists including Angela Davis and phrases and symbols of resistance, elevating their cause—and the titular “people’s cries”—to an art form usually reserved for religious iconography.

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507 West 24th Street, November 2–December 22, 2017;opening reception, 6 p.m.–8 p.m.

Hassel Smith, , 1959–60. Courtesy of Washburn Gallery.

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Bay Area artist Hassel Smith (1915–2007) has only ever had one show in New York, back in 1961. Washburn Gallery returns to that era with an exhibition of abstract works painted by the artist between 1959 and 1961, when he was represented by Irving Blum’s Ferus Gallery in Los Angeles.

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177 Tenth Avenue, November 2–December 22, 2017; private opening reception, 6 p.m.–8 p.m.

Ray Lee, . Courtesy of Sarah Cascone.

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56 Bogart Street, Brooklyn, November 3–December 22, 2017; opening reception, 6 p.m.–9 p.m.

Jorge Tacla, (2016). Courtesy of Cristin Tierney.

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Ahead of his exhibition at the Fundación CorpArtesin Santiago, Chile, opening November 21, Jorge Tacla presents a series of new paintings. His architectural scenes, rendered in oil and cold wax, feature some of the world’s most important museums, libraries, and universities, but with an unsettling lack of human visitors. In these politically contentious times, the artist hopes to remind the viewer of the importance of studying the lessons of history.