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Publication : Kindlin-3 deficiency leads to impaired erythropoiesis and erythrocyte cytoskeleton.

First Author  Szpak D Year  2023
Journal  Blood Adv Volume  7
Issue  9 Pages  1739-1753
PubMed ID  36649586 Mgi Jnum  J:360480
Mgi Id  MGI:7797611 Doi  10.1182/bloodadvances.2022008498
Citation  Szpak D, et al. (2023) Kindlin-3 deficiency leads to impaired erythropoiesis and erythrocyte cytoskeleton. Blood Adv 7(9):1739-1753
abstractText  Kindlin-3 (K3) is critical for the activation of integrin adhesion receptors in hematopoietic cells. In humans and mice, K3 deficiency is associated with impaired immunity and bone development, bleeding, and aberrant erythrocyte shape. To delineate how K3 deficiency (K3KO) contributes to anemia and misshaped erythrocytes, mice deficient in erythroid (K3KOEpoR-cre) or myeloid cell K3 (K3KOLyz2cre), knockin mice expressing mutant K3 (Q597W598 to AA) with reduced integrin-activation function (K3KI), and control wild-type (WT) K3 mice were studied. Both K3-deficient strains and K3KI mice showed anemia at baseline, reduced response to erythropoietin stimulation, and compromised recovery after phenylhydrazine (PHZ)-induced hemolytic anemia as compared with K3WT. Erythroid K3KO and K3 (Q597W598 to AA) showed arrested erythroid differentiation at proerythroblast stage, whereas macrophage K3KO showed decreased erythroblast numbers at all developmental stages of terminal erythroid differentiation because of reduced erythroblastic island (EBI) formation attributable to decreased expression and activation of erythroblast integrin alpha4beta1 and macrophage alphaVbeta3. Peripheral blood smears of K3KOEpoR-cre mice, but not of the other mouse strains, showed numerous aberrant tear drop-shaped erythrocytes. K3 deficiency in these erythrocytes led to disorganized actin cytoskeleton, reduced deformability, and increased osmotic fragility. Mechanistically, K3 directly interacted with F-actin through an actin-binding site K3-LK48. Taken together, these findings document that erythroid and macrophage K3 are critical contributors to erythropoiesis in an integrin-dependent manner, whereas F-actin binding to K3 maintains the membrane cytoskeletal integrity and erythrocyte biconcave shape. The dual function of K3 in erythrocytes and in EBIs establish an important functional role for K3 in normal erythroid function.
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