Proteomic and Transcriptomic Analyses of Placental SLC and ABC Transporters and Implications for Fetal Drug Exposure--A Transporter Elucidation Network (TEN) Presentation

Proteomic and Transcriptomic Analyses of Placental SLC and ABC Transporters and Implications for Fetal Drug Exposure--A Transporter Elucidation Network (TEN) Presentation

Includes a Live Web Event on 07/29/2026 at 3:00 PM (EDT)

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Placental ATP binding cassette (ABC) and solute carrier (SLC) transporters regulate the transfer of nutrients, endogenous compounds, drugs and metabolites between mother and fetus, impacting fetal development and pregnancy outcomes. Identification and accurate quantification of these transporters is critical for predicting nutrient and drug disposition and assessing drug safety throughout pregnancy. Proteomics and transcriptomics offer complementary strategies for identifying and quantifying transporter abundance in placental tissue of varying gestational age. 

The key focus of the NIH‑funded Transporter Elucidation Network (TEN) aims to identify, quantify, and characterize SLC and ABC transporters in the human placenta, the lactating mammary gland, developing gut, and blood-brain barrier.  This webinar will focus on the placenta and feature investigators from the University of Washington Transporter Elucidation Center (UWTEC) and the Integrated Transporter Elucidation Center (InTEC), two of the four Centers that comprise the NIH TEN.

The webinar will begin with proteomic approaches, both targeted and untargeted, and how they offer complementary strategies for identifying and quantifying transporter abundance in placental tissue.  The webinar will then describe newly identified gestational age associated changes in nutrient transporter expression, novel associations between maternal and infant factors, including environmental chemical exposures, and ABC and SLC transporter enrichment in over 250 placentas from the US-based Understanding Pregnancy Signals and Infant Development (UPSIDE) cohort.  Finally, transcriptomic analyses defining the spatial and temporal landscapes of SLC and ABC mRNA expression in human placentas will be presented and discussed. 

Together, this webinar aims to advance understanding of SLC and ABC transporters in fetal nutrient and xenobiotic exposure and highlight emerging technologies that are transforming our ability to characterize placental transporters and their implications for fetal exposure to nutrients and medications.

Learning Objectives:
- Profile high and low abundance ABC and SLC transporter proteins in human placentas
- Compare placental membrane enrichment methods on measured ABC and SLC transporter protein abundance
- Differentiate the roles of targeted versus global proteomics in identifying and quantifying transporters
- Identify potential maternal and infant factors that may impact enrichment of ABC and SLC proteins in human placentas
- Compare nutrient and xenobiotic transporter expression across gestational development

Jaqueline Tiley

Assistant Professor

University of North Carolina at Chapel Hill

Jacqueline B. Tiley, PhD, is an Assistant Professor in the Division of Pharmacotherapy and Experimental Therapeutics at the UNC Eshelman School of Pharmacy. She obtained her MSc in Pharmacy and PhD from the University of Basel in Switzerland. Dr. Tiley completed her postdoctoral training at the University of North Carolina at Chapel Hill. Her research program focuses on disease- and drug-mediated alterations in hepatic and placental transport proteins and its impact on drug disposition and toxicity.

Joanne Wang

Professor

University of Washington

Dr. Joanne Wang is a Professor of Pharmaceutics at the University of Washington School of Pharmacy in Seattle. She earned her PhD in Pharmaceutical Chemistry and completed postdoctoral training at the University of California, San Francisco. Her research focuses on membrane transporters and their roles in xenobiotic and nutrient disposition, pharmacokinetics, and drug-induced toxicity. Her current work examines placental transporters in fetal nutrient uptake and drug exposure and applies systems pharmacology and PBPK modeling to predict transporter-mediated drug exposure during pregnancy and lactation.

Samuel Arnold

Assistant Professor

University of Washington

Dr. Samuel Arnold joined the Department of Pharmaceutics at the University of Washington as an Assistant Professor in 2023, and his research predominantly focuses on characterizing exposure-response relationships for therapeutic treatment of infectious diarrhea. This work includes the development of novel in vitro and in vivo models for enteric pathogens such as Shigella and clinical pharmacology support for clinical trials investigating novel treatments for enteric infections. In addition to his work on enteric infections, Dr. Arnold is the director of the Bioanalysis and Pharmacokinetics Lab at the University of Washington. This lab supports a variety of internal and external projects using mass spectrometry to quantify small molecules and proteins in complex tissue samples.

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Proteomic Strategies for Quantification of Placental Transporters and Fetal Drug Exposure: A Transporter Elucidation Network (TEN) Presentation
07/29/2026 at 3:00 PM (EDT)  |  90 minutes
07/29/2026 at 3:00 PM (EDT)  |  90 minutes ATP binding cassette (ABC) and solute carrier (SLC) placental transport proteins (i.e., transporters) regulate the transfer of nutrients, endogenous compounds, drugs and metabolites between mother and fetus, impacting fetal development and pregnancy outcomes. Identification and accurate quantification of these transporters is critical for predicting nutrient and drug disposition and assessing drug safety throughout pregnancy. Proteomic approaches—both targeted and untargeted—offer complementary strategies for identifying and quantifying transporter abundance in placental tissue of varying gestational age. This webinar will feature work conducted at the University of Washington Transporter Elucidation Center (UWTEC) and the Integrated Transporter Elucidation Center (InTEC) to elucidate which transporters are present in the placenta at different gestational ages and at what levels. The aims of the presentation are to emphasize the pharmacological importance of accurately identifying and quantifying placental transporters at different gestational ages, to predict human fetal drug and nutrient exposure using physiologically based pharmacokinetic (PBPK) modeling, to illustrate how experimental methodology influences data variability, and to highlight novel associations between maternal and infant factors, including environmental chemical exposures, and ABC and SLC transporter enrichment in the placenta.
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