Table 1.

Adhesion of Erythroid Progenitors to Extracellular Matrix Proteins

Substrate% Adhesion
CFU-EMature BFU-EPrimitive BFU-EHEPA1
BSA 6 ± 1 <1 <1 <5 
 n = 19 n = 21 n = 21 n = 3 
Fibronectin 76 ± 2* 5 ± 2* 11 ± 2* 83 ± 5* 
 n = 19 n = 13 n = 16 n = 3 
Laminin 16 ± 1* 12 ± 2* 12 ± 4* 69 ± 4* 
 n = 4 n = 7 n = 7 n = 3 
Collagen types I and III 13 ± 3 <5 <1 78 ± 7* 
 n = 4 n = 2 n = 2 n = 3 
Collagen type IV 15 ± 2* 13 ± 3 <5 82 ± 3* 
 n = 7 n = 2 n = 2 n = 3 
Substrate% Adhesion
CFU-EMature BFU-EPrimitive BFU-EHEPA1
BSA 6 ± 1 <1 <1 <5 
 n = 19 n = 21 n = 21 n = 3 
Fibronectin 76 ± 2* 5 ± 2* 11 ± 2* 83 ± 5* 
 n = 19 n = 13 n = 16 n = 3 
Laminin 16 ± 1* 12 ± 2* 12 ± 4* 69 ± 4* 
 n = 4 n = 7 n = 7 n = 3 
Collagen types I and III 13 ± 3 <5 <1 78 ± 7* 
 n = 4 n = 2 n = 2 n = 3 
Collagen type IV 15 ± 2* 13 ± 3 <5 82 ± 3* 
 n = 7 n = 2 n = 2 n = 3 

Bone marrow cells were incubated in wells coated with the indicated substrates. The unattached and attached populations were then assayed for the presence of CFU-Es, mature BFU-Es, and primitive BFU-Es. Hepal cell adhesion assays were performed as previously described (Patel et al39 ). Briefly, the cells were metabollically labeled and incubated in wells coated with the indicated substrates. The ratio of adherent cpm to the input cpm was then calculated. All results are expressed as the mean percent cell adhesion ± SEM.

*

P ≤ .02.

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