Enhanced human Blood-Brain Barrier Chip performs in vivo-like drug and antibody transport

Microfluidic Organ Chip model of human blood-brain barrier that recapitulates in vivo barrier functions offers new preclinical tool for development of brain-targeting therapeutics

By Benjamin Boettner

(BOSTON) — Like airport security barriers that either clear authorized or block unauthorized travelers and their luggage from accessing central operation areas, the blood-brain barrier (BBB) tightly controls the transport of essential nutrients and energy metabolites into the brain and staves off unwanted substances circulating in the blood stream. Importantly, its highly organized structure of thin blood vessels and supporting cells is also the major obstacle preventing life-saving drugs from reaching the brain in order to effectively treat cancer, neurodegeneration, and other diseases of the central nervous system. In a number of brain diseases, the BBB can also locally break down, causing neurotoxic substances, blood cells, and pathogens to leak into the brain and wreak irreparable havoc.

To study the BBB and drug transport across it, researchers have mostly relied on animal models such as mice. However, the precise make-up and transport functions of BBBs in those models can significantly differ from those in human patients, which makes them unreliable for the prediction of drug delivery and therapeutic efficacies. Also, in vitro models attempting to recreate the human BBB using primary brain tissue-derived cells thus far have not been able to mimic the BBB’s physical barrier, transport functions, and drug and antibody shuttling activities closely enough to be useful as therapeutic development tools.

This illustration shows how In the Blood-Brain-Barrier (BBB), thin endothelial capillaries (red) are wrapped by supporting pericytes (green) and astrocytes (yellow), enabling them to generate a tight barrier with highly selective transport functions for molecules entering the brain fluid from the blood stream. Credit: Wyss Institute at Harvard University

Now, a team led by Donald Ingber, M.D.,Ph.D. at Harvard’s Wyss Institute for Biologically Inspired Engineering has overcome these limitations by leveraging its microfluidic Organs-on-Chips (Organ Chips) technology in combination with a developmentally-inspired hypoxia-mimicking approach to differentiate human pluripotent stem (iPS) cells into brain microvascular endothelial cells (BMVECs). The resulting “hypoxia-enhanced BBB Chip” recapitulates cellular organization, tight barrier functions, and transport abilities of the human BBB; and it allows the transport of drugs and therapeutic antibodies in a way that more closely mimics transport across the BBB in vivo than existing in vitro systems. Their study is reported in Nature Communications.

“Our approach to modeling drug and antibody shuttling across the human BBB in vitro with such high and unprecedented fidelity presents a significant advance over existing capabilities in this enormously challenging research area,” said Ingber, who is the Wyss Institute’s Founding Director. “It addresses a critical need in drug development programs throughout the pharma and biotech world that we now aim to help overcome with a dedicated ‘Brain Targeting Program’ at the Wyss Institute using our unique talent and resources.” Ingber is also the Judah Folkman Professor of Vascular Biology at Harvard Medical School and the Vascular Biology Program at Boston Children’s Hospital, as well as Professor of Bioengineering at the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS).

Our approach to modeling drug and antibody shuttling across the human BBB in vitro with such high and unprecedented fidelity presents a significant advance over existing capabilities in this enormously challenging research area

Don Ingber

The BBB consists of thin capillary blood vessels formed by BMVECs, multifunctional cells known as pericytes that wrap themselves around the outside of the vessels, and star-shaped astrocytes, which are non-neuronal brain cells that also contact blood vessels with foot-like processes. In the presence of pericytes and astrocytes, endothelial cells can generate the tightly sealed vessel wall barrier typical of the human BBB.

Ingber’s team first differentiated human iPS cells into brain endothelial cells in the culture dish using a method that had been previously developed by co-author Eric Shusta, Ph.D., Professor of Chemical and Biological Engineering at University of Wisconsin-Madison, but with the added power of bioinspiration. “Because in the embryo the BBB forms under low-oxygen conditions (hypoxia), we differentiated iPS cells for an extended time in an atmosphere with only 5% instead of the normal 20% oxygen concentration,” said co-first author Tae-Eun Park, Ph.D. “As a result, the iPS cells initiated a developmental program very similar to that in the embryo, producing BMVECs that exhibited higher functionality than BMVECs generated in normal oxygen conditions.” Park is a former Postdoctoral Fellow on Ingber’s team who is now an Assistant Professor at Ulsan National Institute of Science and Technology in the Republic of Korea.

Building on a previous human BBB model, the researchers next transferred the hypoxia-induced human BMVECs into one of two parallel channels of a microfluidic Organ Chip device that are divided by a porous membrane and continuously perfused with medium. The other channel was populated with a mixture of primary human brain pericytes and astrocytes. Following an additional day of hypoxia treatment, the human BBB Chip could be stably maintained for at least 14 days at normal oxygen concentrations, which is far longer than past in vitro human BBB models attempted in the past.

In the enhanced human BBB Chip, endothelial cells derived from induced human pluripotent stem cells in a development-inspired process, form a microvessel in the lower of two parallel microfluidic channels (lower images), while pericytes and astrocytes populating the upper channel connect to the microvessel across a dividing porous membrane. Credit: Wyss Institute at Harvard University

Under the shear stress of the fluids perfusing the BBB Chip, the BMVECs go on to form a blood vessel, and develop a dense interface with pericytes aligning with them on the other side of the porous membrane, as well as with astrocytes extending processes towards them through small openings in the membrane. “The distinct morphology of the engineered BBB is paralleled by the formation of a tighter barrier containing elevated numbers of selective transport and drug shuttle systems compared to control BBBs that we generated without hypoxia or fluid shear stress, or with endothelium derived from adult brain instead of iPS cells,” said Nur Mustafaoglu, Ph.D., a co-first author on the study and Postdoctoral Fellow working on Ingber’s team. “Moreover, we could emulate effects of treatment strategies in patients in the clinic. For example, we reversibly opened the BBB for a short time by increasing the concentration of a mannitol solute [osmolarity] to allow the passage of large drugs like the anti-cancer antibody Cetuximab.”

To provide additional proof that the hypoxia-enhanced human BBB Chip can be utilized as an effective tool for studying drug delivery to the brain, the team investigated a series of transport mechanisms that either prevent drugs from reaching their targets in the brain by pumping them back into the blood stream (efflux), or that, in contrast, allow the selective transport of nutrients and drugs across the BBB (transcytosis).

“When we specifically blocked the function of P-gp, a key endothelial efflux pump, we could substantially increase the transport of the anti-cancer drug doxorubicin from the vascular channel to the brain channel, very similarly to what has been observed in human patients,” said Park. “Thus, our in vitro system could be used to identify new approaches to reduce efflux and thus facilitate drug transport into the brain in the future.”

In other efforts, drug developers are trying to harness “receptor-mediated transcytosis” as a vehicle for shuttling drug-loaded nanoparticles, larger chemical and protein drugs, as well as therapeutic antibodies across the BBB. “The hypoxia-enhanced human BBB Chip recapitulates the function of critical transcytosis pathways, such as those used by the LRP-1 and transferrin receptors responsible for taking up vital lipoproteins and iron from circulating blood and releasing them into the brain on the other side of the BBB. By harnessing those receptors using different preclinical strategies, we can faithfully mimic the previously demonstrated shuttling of therapeutic antibodies that target transferrin receptors in vivo, while maintaining the BBB’s integrity in vitro,” said Mustafaoglu.

We aim to collaborate with multiple biopharmaceutical partners in a pre-competitive relationship to develop shuttles offering exceptional efficacy and engineering flexibility for incorporation into antibody and protein drugs, because this is so badly needed by patients and the whole field.

James Gorman

Based on these findings, the Wyss Institute has initiated a “Brain Targeting Program.”  “Initially, the BBB Transport Program aims to discover new shuttle targets that are enriched on the BMVEC vascular surface, using novel transcriptomics, proteomics, and iPS cell approaches. In parallel, we are developing fully human antibody shuttles directed against known shuttle targets with enhanced brain-targeting capabilities,” said James Gorman, M.D., Ph.D., the Staff Lead on the Advanced Technology Team for the BBB Transport Program working with Ingber. “We aim to collaborate with multiple biopharmaceutical partners in a pre-competitive relationship to develop shuttles offering exceptional efficacy and engineering flexibility for incorporation into antibody and protein drugs, because this is so badly needed by patients and the whole field.”

The authors think that in addition to drug development studies, the hypoxia-enhanced human BBB Chip can also be used to model aspects of brain diseases that affect the BBB such as Alzheimer’s and Parkinson’s disease, and to advance personalized medicine approaches by using patient-derived iPS cells.

Other authors on the study are past and present members of Ingber’s team, including former Postdoctoral Fellow Anna Herland, Ph.D., and former Graduate Student Edward Fitzgerald; former Research Assistant Ryan Hasselkus, Research Associate Robert Mannix, Ph.D., Senior Staff Scientist Rachelle Prantil-Baun, Ph.D., Senior Staff Scientist Alexander Watters, Ph.D., former Staff Engineer Olivier Henry, Ph.D., Research Assistant Maximilian Benz, and former Research Assistant Henry Sanchez; Heather McCrea, M.D., and Liliana Christova Goumnerova, M.D., at Boston Children’s Hospital; Sean Palecek, Ph.D., Professor, and Hannah Song William, Ph.D., at University of Wisconsin-Madison. The study was funded by Harvard’s Wyss Institute for Biologically Inspired Engineering, the Defense Advanced Research Projects Agency (DARPA), the National Research Foundation of Korea, and the Knut and Alice Wallenberg Foundation.