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. 2023 Dec 19;21(3):369–377. doi: 10.1007/s13770-023-00600-6

Table 2.

Overview of the three dimensional intestinal in vitro models with epithelium and lamina propria compartments

Epithelial layer Lamina Propria layer Scaffold Barrier competency Reference
Permeability TEER TEER compared to native small intestine
Caco-2 and HT29-MTX cells

Human primary embryonic fibroblasts

Human THP-1 derived macrophages

Rat tail collagen

*app. 11 × 10–6 cm/s

c: app. 4.5 × 10–6 cm/s

app. 500 Ω*cm2

c: app. 2000 Ω*cm2

[7]
Caco-2 and HT29-MTX cells Human CCD-18co intestinal myofibroblasts Matrigel NS

app. 250 Ω*cm2

c: app. 1750 Ω*cm2

[8]
Human primary ileum organoids Human primary ileum fibroblasts Collagen coated plates NS

70–200 Ω*cm2

c: NS

 →  [9]
Human primary intestinal organoids Human CC-2902 intestinal myofibroblasts Collagen coated plates NS NS NS [10]
Caco-2 cells Human CCD-18co intestinal myofibroblasts or human neonatal dermal fibroblasts Alvetex® scaffold

+app. 2.5 × 10–6 cm/s

c: app. 0.5 × 10–6 cm/s

50–200 Ω*cm2

c: app. 2000 Ω*cm2

 →  [11]
Caco-2 and HT29-MTX cells Human primary intestinal fibroblasts Rat tail collagen

*app. 2.4 × 10–6 cm/s

c: < 0.5 × 10–7 cm/s

app. 200 Ω*cm2

c: app. 700 Ω*cm2

[12]
Caco-2 cells 3T3 mouse embryonic fibroblasts Rat tail collagen type 1

+1.84 ± 0.20 × 10–7 cm/s

c: 6.47 ± 1.59 × 10–8 cm/s

app. 1000 Ω*cm2

c: app. 2200 Ω*cm2

[13]

TEER of small intestine (in vivo): 50–100Ωcm2 [73]. Models of [9] and [10] were maintained at the air–liquid interface after 4 days submerged, the rest of the models were submerged. All models were cultured on porous transwell membranes

c Control, * Fluorescein, + Lucifer yellow ↑ Higher, → Similar, NS not studied