Public Schema V2 · Lung Census V1

16HBE14o-

A02 · stable entity ID: LUNG-ENT-001

Provenance and Evidence

Species
Homo sapiens
Tissue origin
Lung
Provenance summary
Lung V1 frozen scientific record
Evidence summary
Lung V1 frozen scientific record
Identity caveat
NOT_ASSESSED
Public omics readiness
NOT ASSESSED

Relationships

No parent relationship recorded.

Disease Applications

Disease context

Asthma

Airway inflammatory disease

LITERATURE SUPPORTED
Stimulus
House dust mite extract
Experimental context
16HBE + HDM
Stimulus parameters
dose: NOT_REPORTED; exposure duration: NOT_REPORTED

Application purpose

  • Asthma-related epithelial inflammatory response

Evidence summary: Directly supports 16HBE14o- (the canonical entity for the 16HBE query) as an in-vitro HDM airway-inflammation application context. The human airway epithelial line 16HBE14o- was exposed to house dust mite and assessed for CCL20 secretion and signaling pathways; findings were compared with primary bronchial cells. Supports HDM-driven barrier and inflammatory-response readouts in 16HBE airway epithelium. HDM effects on calcium signaling, barrier function and CCL20 release were tested in human bronchial epithelial 16HBE cells alongside primary bronchial epithelial cells.

Interpretation: Used to study HDM-associated bronchial epithelial inflammatory and barrier responses in 16HBE14o-.

Limitation: An immortalized line and a defined chemokine/signaling endpoint do not model all asthma biology or establish disease fidelity. The cell line is an immortalized bronchial model and cannot capture donor heterogeneity or the full asthma airway environment.

Supporting references

  • PMID 19178937 — Innate immune responses of airway epithelium to house dust mite are mediated through beta-glucan-dependent pathways
  • PMID 23915187 — House dust mite-induced calcium signaling instigates epithelial barrier dysfunction and CCL20 production

Disease application evidence describes documented experimental use. It does not change model identity, database role, physiological relevance, Disease Fidelity, or overall model ranking.

Physiological Relevance

No formal PR assessment available in PUBLIC_RC1. This does not imply low relevance, failure, or a recommendation against the model.

Uncertainty and Limitations

No structured uncertainty flag is recorded.

Analysis layers

Physiological Relevance and Disease Fidelity are separate analysis layers. No overall score or ranking is generated by this page.

Physiological Relevance
NOT_ASSESSED
Disease Fidelity
NOT_ASSESSED
Availability
REPOSITORY OR VENDOR SIGNAL

Lung V1 scientific context

Coverage
2 adequate · 4 partial · 2 under-covered
Saturation
SATURATION LIMITED BY MODEL ECOSYSTEM
Module state
FROZEN
Freeze ID
LUNG-CENSUS-V1-FROZEN

These module-level statements preserve the frozen scientific limitation context; they do not rank or reclassify this entity.