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Blocking the α4 integrin–paxillin interaction selectively impairs mononuclear leukocyte recruitment to an inflammatory site
Chloé C. Féral, David M. Rose, Jaewon Han, Norma Fox, Gregg J. Silverman, Kenneth Kaushansky, Mark H. Ginsberg
Chloé C. Féral, David M. Rose, Jaewon Han, Norma Fox, Gregg J. Silverman, Kenneth Kaushansky, Mark H. Ginsberg
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Research Article Immunology

Blocking the α4 integrin–paxillin interaction selectively impairs mononuclear leukocyte recruitment to an inflammatory site

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Abstract

Antagonists to α4 integrin show promise for several autoimmune and inflammatory diseases but may exhibit mechanism-based toxicities. We tested the capacity of blockade of α4 integrin signaling to perturb functions involved in inflammation, while limiting potential adverse effects. We generated and characterized mice bearing a Y991A mutation in α4 integrin [α4(Y991A) mice], which blocks paxillin binding and inhibits α4 integrin signals that support leukocyte migration. In contrast to the embryonic-lethal phenotype of α4 integrin–null mice, mice bearing the α4(Y991A) mutation were viable and fertile; however, they exhibited defective recruitment of mononuclear leukocytes into thioglycollate-induced peritonitis. α4 Integrins are essential for definitive hematopoiesis; however, the α4(Y991A) mice had intact lymphohematopoiesis and, with the exception of reduced Peyer’s patches, normal architecture and cellularity of secondary lymphoid tissues. We conclude that interference with α4 integrin signaling can selectively impair mononuclear leukocyte recruitment to sites of inflammation while sparing vital functions of α4 integrins in development and hematopoiesis.

Authors

Chloé C. Féral, David M. Rose, Jaewon Han, Norma Fox, Gregg J. Silverman, Kenneth Kaushansky, Mark H. Ginsberg

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Figure 6

The α4 integrin–paxillin interaction is not required for normal architecture and lymphocyte distribution within the spleen.

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The α4 integrin–paxillin interaction is not required for normal architec...
(A) Histology of spleens from WT and α4(Y991A) is shown. Sections from paraffin embedded spleens were stained with H&E. Immunofluorescence of splenic sections stained with MOMA-1 (green) to detect macrophages and B220 (red) to detect B cells is also shown. The locations of macrophages (Mac), follicular B cells (FB), and marginal zone B (MZB) cells are indicated. (B) The relative percentage of T and B cells in the spleen is shown. Splenocytes from WT and α4(Y991A) mice were analyzed by flow cytometry for CD3 (T cell marker) and B220 (B cell marker). (C) The relative percentage of B cell subpopulations in the spleen is shown. Cells were stained for B220, CD21/35, and CD23, and flow cytometry was used to distinguish marginal zone B cells (CD21/35+CD23–), follicular B cells (CD21/35+CD23+), and immature B cells (CD21/35–CD23–). (D) Follicular architecture in spleens from WT and α4(Y991A) mice. Immunofluorescence of tissue sections was performed with anti-IgM (red) and anti-IgD (green) to distinguish the position of B cell follicles with a rim of marginal zone B cells (IgM+IgD–). Arrows indicate the marginal zone around the follicle. Results are representative of 6–8 different mice. Magnification, ×4 (A, top); ×20 (A, bottom, and D).

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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