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( A ) Schematic diagram showing the generation of littermate control and Vav1-cre ; <t>Rbfox1</t> fl/fl mice. ( B to D ) Cellularity (B), HSC frequency (C), and HSC number (D) in the bone marrow of one hindlimb from control and Vav1-cre ; Rbfox1 fl/fl mice. ( E ) Donor-derived blood cells in recipients transplanted with bone marrow cells from control or Vav1-cre ; Rbfox1 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 7 recipients for control and n = 6 recipients for Vav1-cre ; Rbfox1 fl/fl mice. ( F ) Schematic diagram showing the generation of littermate Rbfox1 fl/fl ; Rbfox2 fl/fl control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( G to I ) Cellularity (G), HSC frequency (H), and HSC number (I) in the bone marrow of one hindlimb from littermate control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( J to L ) Relative fold changes of cellularity (J), HSC frequency (K), and HSC number (L) in the bone marrow of Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding littermate Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. ( M ) Donor-derived blood cells in recipients transplanted with bone marrow cells from Rbfox1 fl/fl ; Rbfox2 fl/fl control or littermate Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 8 recipients for control and n = 9 recipients for Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( N ) Relative fold changes of overall reconstitution 16 weeks after transplantation by bone marrow cells from Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. Data are means ± SEM. * P < 0.05; ** P < 0.01; *** P < 0.001. Statistical analyses were performed with t test in (B) to (D), (G) to (L), and (N), and with two-way ANOVA followed by Bonferroni’s multiple comparisons test in (E) and (M). The diagrams in (A) and (F) were created using BioRender. L. Gao (2025); https://BioRender.com/f3aye8s .
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( A ) Schematic diagram showing the generation of littermate control and Vav1-cre ; <t>Rbfox1</t> fl/fl mice. ( B to D ) Cellularity (B), HSC frequency (C), and HSC number (D) in the bone marrow of one hindlimb from control and Vav1-cre ; Rbfox1 fl/fl mice. ( E ) Donor-derived blood cells in recipients transplanted with bone marrow cells from control or Vav1-cre ; Rbfox1 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 7 recipients for control and n = 6 recipients for Vav1-cre ; Rbfox1 fl/fl mice. ( F ) Schematic diagram showing the generation of littermate Rbfox1 fl/fl ; Rbfox2 fl/fl control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( G to I ) Cellularity (G), HSC frequency (H), and HSC number (I) in the bone marrow of one hindlimb from littermate control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( J to L ) Relative fold changes of cellularity (J), HSC frequency (K), and HSC number (L) in the bone marrow of Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding littermate Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. ( M ) Donor-derived blood cells in recipients transplanted with bone marrow cells from Rbfox1 fl/fl ; Rbfox2 fl/fl control or littermate Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 8 recipients for control and n = 9 recipients for Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( N ) Relative fold changes of overall reconstitution 16 weeks after transplantation by bone marrow cells from Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. Data are means ± SEM. * P < 0.05; ** P < 0.01; *** P < 0.001. Statistical analyses were performed with t test in (B) to (D), (G) to (L), and (N), and with two-way ANOVA followed by Bonferroni’s multiple comparisons test in (E) and (M). The diagrams in (A) and (F) were created using BioRender. L. Gao (2025); https://BioRender.com/f3aye8s .
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( A ) Schematic diagram showing the generation of littermate control and Vav1-cre ; Rbfox1 fl/fl mice. ( B to D ) Cellularity (B), HSC frequency (C), and HSC number (D) in the bone marrow of one hindlimb from control and Vav1-cre ; Rbfox1 fl/fl mice. ( E ) Donor-derived blood cells in recipients transplanted with bone marrow cells from control or Vav1-cre ; Rbfox1 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 7 recipients for control and n = 6 recipients for Vav1-cre ; Rbfox1 fl/fl mice. ( F ) Schematic diagram showing the generation of littermate Rbfox1 fl/fl ; Rbfox2 fl/fl control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( G to I ) Cellularity (G), HSC frequency (H), and HSC number (I) in the bone marrow of one hindlimb from littermate control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( J to L ) Relative fold changes of cellularity (J), HSC frequency (K), and HSC number (L) in the bone marrow of Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding littermate Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. ( M ) Donor-derived blood cells in recipients transplanted with bone marrow cells from Rbfox1 fl/fl ; Rbfox2 fl/fl control or littermate Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 8 recipients for control and n = 9 recipients for Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( N ) Relative fold changes of overall reconstitution 16 weeks after transplantation by bone marrow cells from Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. Data are means ± SEM. * P < 0.05; ** P < 0.01; *** P < 0.001. Statistical analyses were performed with t test in (B) to (D), (G) to (L), and (N), and with two-way ANOVA followed by Bonferroni’s multiple comparisons test in (E) and (M). The diagrams in (A) and (F) were created using BioRender. L. Gao (2025); https://BioRender.com/f3aye8s .

Journal: Science Advances

Article Title: Rbfox2 selectively governs hematopoietic stem cell self-renewal by regulating proteostasis

doi: 10.1126/sciadv.aea7451

Figure Lengend Snippet: ( A ) Schematic diagram showing the generation of littermate control and Vav1-cre ; Rbfox1 fl/fl mice. ( B to D ) Cellularity (B), HSC frequency (C), and HSC number (D) in the bone marrow of one hindlimb from control and Vav1-cre ; Rbfox1 fl/fl mice. ( E ) Donor-derived blood cells in recipients transplanted with bone marrow cells from control or Vav1-cre ; Rbfox1 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 7 recipients for control and n = 6 recipients for Vav1-cre ; Rbfox1 fl/fl mice. ( F ) Schematic diagram showing the generation of littermate Rbfox1 fl/fl ; Rbfox2 fl/fl control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( G to I ) Cellularity (G), HSC frequency (H), and HSC number (I) in the bone marrow of one hindlimb from littermate control and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( J to L ) Relative fold changes of cellularity (J), HSC frequency (K), and HSC number (L) in the bone marrow of Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding littermate Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. ( M ) Donor-derived blood cells in recipients transplanted with bone marrow cells from Rbfox1 fl/fl ; Rbfox2 fl/fl control or littermate Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice, along with competitor cells. Two pairs of donor mice were used. A total of n = 8 recipients for control and n = 9 recipients for Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. ( N ) Relative fold changes of overall reconstitution 16 weeks after transplantation by bone marrow cells from Vav1-cre ; Rbfox2 fl/fl and Vav1-cre ; Rbfox1 fl/fl ; Rbfox2 fl/fl mice. Fold changes were normalized to corresponding Rbfox2 fl/fl and Rbfox1 fl/fl ; Rbfox2 fl/fl controls, respectively. Data are means ± SEM. * P < 0.05; ** P < 0.01; *** P < 0.001. Statistical analyses were performed with t test in (B) to (D), (G) to (L), and (N), and with two-way ANOVA followed by Bonferroni’s multiple comparisons test in (E) and (M). The diagrams in (A) and (F) were created using BioRender. L. Gao (2025); https://BioRender.com/f3aye8s .

Article Snippet: Vav1-cre , Mx1-cre , Rbfox1 fl , and Rbfox2 fl ( ) mice were obtained from the Jackson Laboratory and maintained on C57BL/6 background.

Techniques: Control, Derivative Assay, Transplantation Assay