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Utilizing biodegradable porous silicon membranes as a novel design for lung-on-a-chip microfluidic devices to investigate extracellular matrix interactions.

Award Number: SC3GM141838
ORGANIZATION: NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

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Utilizing biodegradable porous silicon membranes as a novel design for lung-on-a-chip microfluidic devices to investigate extracellular matrix interactions. - Project Summary Identifying the cellular pathways that promote disease or which prospective therapies are effective relies upon appropriate mammalian models. Therefore, there is an urgent need for advanced human model systems that can accurately reproduce human anatomy and physiology to help predict human disease progression and as- sess potential treatment options. The long-term goal is to utilize a novel in vitro lung-on-a-chip (LOAC) microflu- idic device to predict how xenobiotics lead to inflammatory, fibrotic and immunomodulatory pulmonary diseases in humans. The overall objective is to create the first fully organic LOAC that is structurally supported by a cell- derived extracellular matrix (ECM) and includes innate immune cells to simulate organ-level functionality. The rationale for the proposed research is to employ the unique properties of porous silicon (PSi) not previously explored to revolutionize the field of material science in the fabrication of microfluidic platforms that incorporates dynamic ECM changes. Guided by strong preliminary data, the overall objective will be accomplished by pursing the following three specific aims: 1) Identify the optimal parameters and cellular mechanisms to dissolve ultrathin porous silicon during long-term culture; 2) Determine the extent to which co-cultured cells within the LOAC se- crete and create their own ECM; and 3) Develop a multicellular alveolar structure to activate immune cells leading to extravasation and ECM remodeling using an in vitro model of pulmonary hypertension. Under the first aim, the working hypothesis based on preliminary data is that human macrophages (MACs) are essential to modify and dissolve PSi. Dissolution rates of PSi will be quantified through scanning electron microscopy (SEM) and surface analysis will be completed by atomic force microscopy (AFM) to reproducibly create flexible, structurally intact membranes. Under the second aim, the working hypothesis is that endothelial cells (ECs) will express and secrete cell-derived ECM proteins. Secretion of de novo synthesized ECM components will be quantified through RT-PCR, confocal immunofluorescence (IF) microscopy and AFM. The third aim based on preliminary data in- dicate epithelial cells (EPCs), ECs and MACs can be successfully co-cultured and are viable during long-term culture on PSi membranes. The working hypothesis is in the presence of hypoxic conditions, MACs will become activated and release soluble mediators leading to apoptosis of ECs and increased ECM remodeling that will be quantified through confocal IF microscopy and live cell imaging. The proposed research is innovative, in our opinion, because it represents a substantive departure from the status quo by utilizing the unique characteristics of PSi, which is a biocompatible and biodegradable material. In addition, utilizing PSi provides the capability to create a cell specific ECM that will release biochemical cues including growth factors and extracellular protein- ases. The proposed research is significant because it is expected to have broad translational importance in the prevention and treatment of a wide range of pulmonary diseases. Finally, therapeutic advancements in the de- velopment of PSi nanomaterials and factors that lead to degradation in vivo are expected.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2024 ( Subtotal = $97,500 )
2024	2024	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	000	4	4/5/2024	NON-COMPETING CONTINUATION	$87,750
2024	2024	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	001	4	6/18/2024	NON-COMPETING CONTINUATION	$9,750
														Subtotal = $97,500

Issue Date FY: 2023 ( Subtotal = $97,500 )
2023	2023	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	000	3	4/28/2023	NON-COMPETING CONTINUATION	$97,500
														Subtotal = $97,500

Issue Date FY: 2022 ( Subtotal = $118,255 )
2022	2022	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	002	2	6/27/2022	NON-COMPETING CONTINUATION	$9,750
2022	2022	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	001	2	6/15/2022	SUPPLEMENT FOR EXPANSION	$20,755
2022	2022	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	000	2	4/8/2022	NON-COMPETING CONTINUATION	$87,750
														Subtotal = $118,255

Issue Date FY: 2021 ( Subtotal = $97,500 )
2021	2021	FORT LEWIS COLLEGE	1000 RIM DR	DURANGO	CO	81301	LA PLATA	USA	Biomedical Research and Research Training	000	1	4/30/2021	NEW	$97,500
														Subtotal = $97,500

Grand Total All Awards = $410,755

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Utilizing biodegradable porous silicon membranes as a novel design for lung-on-a-chip microfluidic devices to investigate extracellular matrix interactions.

Award Number: SC3GM141838

ORGANIZATION: NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

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