Immortalized Human Fungiform Taste Cells-SV40

Immortalized Human Fungiform Taste Cells-SV40

Cat.No.: CSC-I9103L

Species: Homo sapiens

Source: Oral

Culture Properties: Adherent

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Cat.No.
CSC-I9103L
Description
Species
Homo sapiens
Source
Oral
Culture Properties
Adherent
Immortalization Method
Serial passaging and transduction with recombinant lentiviruses carrying SV40 Large T antigen
Application
For Research Use Only
Storage
Directly and immediately transfer cells from dry ice to liquid nitrogen upon receiving and keep the cells in liquid nitrogen until cell culture needed for experiments.

Note: Never can cells be kept at -20 °C.
Shipping
Dry Ice.
Recommended Products
CIK-HT003 HT® Lenti-SV40T Immortalization Kit
Quality Control
Real Time PCR was used to quantify SV40 gene expression in immortalized cell line.
BioSafety Level
II
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Immortalized human fungiform taste cells-SV40 (HTC/SV40) are generated by introducing the SV40 large T antigen into primary cells derived from human fungiform papillae. This approach overcomes the scarcity, limited lifespan, and donor variability of primary human taste cells, providing a continuous, scalable, and reproducible in vitro model.

These cells are designed to preserve key features of taste receptor cells, including expression of TAS1R and TAS2R receptor families, GNAT3 (gustducin), PLCβ2, IP3R3, TRPM5, and epithelial/taste progenitor markers. Depending on the subset, they can support functional studies of sweet, umami, bitter, sour, and salt transduction using calcium imaging, cAMP/ATP measurement, or electrophysiology.

Advantages include human relevance, indefinite expansion, consistent batch performance, and compatibility with high-throughput screening, siRNA/CRISPR perturbation, immunostaining, qPCR, and Western blot. They enable mechanistic studies of taste receptor signaling, ligand specificity, and taste modulation, and support discovery of sweeteners, umami enhancers, bitter blockers, salt substitutes, and taste-masking excipients. They are also useful for modeling taste dysfunction associated with infection (e.g., SARS-CoV-2), inflammation, aging, and metabolic disease.

Limitations: Immortalized cultures may not fully recapitulate the heterogeneous taste bud microenvironment or all primary cell phenotypes. Validation against primary human fungiform taste cells is recommended when physiological fidelity is critical. Overall, HTC/SV40 offer a practical, human-relevant, and scalable platform for taste biology and chemosensory translational research.

Neuropeptide Y and Peptide YY Modulate Bitter And Fatty Acid Responses in Human Fungiform Taste Bud Cells

Previous studies suggest that manipulation of neuropeptide Y (NPY) family peptide signaling can impact upon taste-related behavior, but it remains unclear whether these are mediated by changes in taste information processed by taste bud cells (TBCs), the primary sensory organs of the gustatory system.

In this report, we identify a complex modulatory role for NPY family peptides in shaping the tastant-evoked responses of human TBCs. Using an immortalized human fungiform (HuFF) taste cell line, we show that NPY and peptide YY (PYY), along with NPY receptor subtypes 1 and 2 (NPY1R and NPY2R), are expressed in TBCs. Importantly, NPY and PYY modulated the functional responses (assessed by calcium imaging and measurements of neurotransmitter release) of TBCs to bitter and fatty acid stimuli. The nature of modulation (i.e., enhancement or diminishment) was dependent not only on the peptide but also on the taste modality in question. Application of NPY1R and NPY2R antagonists indicated that the differential impacts of these peptides on TBC response parameters were mediated by differential NPY receptor activation. These data suggest that NPY family peptides directly and intricately modify gustatory sensory input by shaping TBC signaling.

Chronic Exposure to PYY or NPY Modulates Bitter and Fatty Acid Responsiveness.
Fig. 1. Preincubation with PYY and NPY impacts HuFF response rates (Iyer, Satya, et al., 2026).

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