Research

Harvard 3D bioprinting research mimics kidney function like never before

Scientists working with theaward winningLewis LabatHarvard University犯了一个significant advancement in the development of 3D bioprinted kidney models. Building onfoundational workpublished in 2016, a new paper in theProceedings of the National Academy of Sciences(PNAS) discusses the absorption of substances in 3D bioprinted models of a kidney’s promixal tubule.

Lab leadProfessor Jennifer Lewis, who is also core faculty member of Harvard’sWyss Institute for Biologically Inspired Engineering,注释, “Our new 3D kidney model is an exciting advance as it more fully recapitulates the proximal tubule segments found in native kidney tissue.”

“Beyond its immediate applications for drug screening and disease modelling, we are also exploring whether these living devices can be used to augment kidney dialysis.”

3D bioprinting for better drug screening

Proximal tubules are the microscopic segments of a kidney responsible for regulating the pH of filtrate. Part of the kidney’s nephron, the cell walls of proximal tubules can reabsorb valuable nutrients from the filtrate back into the kidney, and also redirect waste for secretion. By 3D printing these minute structures, the Lewis Lab’s aim is to recreate the behavior of kidney tissue for further study outside of the body. Eventually, this could lead to the blue-sky view of bio-engineered organs for transplant. More pressing though, is these models’ potential impact on pharmaceutical development.

The independent perfusion of a 3D bioprinted proximal tubule and vascular channel running in parallel. Clip via Wyss Institute at Harvard University

Annie Moisan, study co-author and Principal Scientist at the lab’s industry partner罗氏创新中心巴塞尔, explains, “Our system could enable the screening of focused drug libraries for renal toxicity and thus help reduce animal experiments.”

“我和其他人继续努力提高此类模型的生理相关性,例如,通过纳入患者特异性和患病细胞的努力感到非常兴奋,因为个性化的疗效和安全性是预测对药物临床反应的最终目标。”

Simulating the activity of diabetes

Previously, the Lewis Lab had managed to 3D bioprint a singular, perfusable proximal tubule. The key development in this new paper is the addition of a perfusable blood vessel that runs alongside the tubule.

含有近端小管(绿色)和血管(红色)的毫米芯片的制造过程。通过PNAS图像
含有近端小管(绿色)和血管(红色)的毫米芯片的制造过程。通过PNAS图像

Both of the 3D bioprinted structures contain living cells. In experiments, the team studied the tubule’s ability to move glucose into the blood vessel. The team also simulated the occurrence of hyperglycemia – the high glucose levels that occur in diabetes patients. “We found that high levels of glucose transported to endothelial cells in the vascular compartment caused cell damage,” said study co-author and Lewis Lab Research Associate Kimberly Homan.

“By circulating a drug through the tubule that specifically inhibits a major glucose transporter in proximal tubule epithelial cells, we prevented those harmful changes from happening to the endothelial cells in the adjacent vessels.”

Further, as discussed in the body of the study, “Although these experiments focused on acute glucotoxicity, we believe that longitudinal studies carried out under conditions that mimic chronic hyperglycemia may provide valuable insights into treatments of diabetic vascular diseases.”

Renal reabsorption in 3D vascularized proximal tubule models”在PNASjournal. It is co-authored byNeil Y. C. Lin,Kimberly A. Homan,Sanlin S. Robinson,David B. Kolesky,内森·杜阿尔特(Nathan Duarte),Annie Moisan, and詹妮弗·刘易斯(Jennifer A. Lewis).

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Featured image shows 3D bioprinting a proximal tubule (green) and blood vessel (red). Image via Wyss Institute at Harvard University