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Coronal brain sections from Shank3 WT and KO mice of corpus callosum (CC) have been used for all analyses. A Brain sections from P7 WT and Shank3KO mice stained for MBP and MBP RNA scope. MBP protein and RNA intensity were normalized to mean value. MBP positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p** < 0.01, n = 3 animals. Scale bar = 200 μm. B Immunostaining for MBP and NFH SMI32 and analysis of myelinating and non-myelinating oligodendrocytes in P7 CC. Myelinating and non-myelinating cells were shown in the percentage of total MBP positive cells. Mean ± SD. Student’s Unpaired t test, p**** < 0.0001, n = 3 animals. Scale bar = 100 μm. C P7, P21 and P140 brain section were stained for Olig2 and <t>CC1.</t> Cell number of Olig2 + CC1+ cells were analysed in CC. Data were shown in the percentage of DAPI and Olig2 respectively. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm. D P7 brain section were stained for Ki67, Iba1 and GFAP and proliferation of Ki67+cells was analysed in medial and lateral CC separately. Ki67 positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm.
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Coronal brain sections from Shank3 WT and KO mice of corpus callosum (CC) have been used for all analyses. A Brain sections from P7 WT and Shank3KO mice stained for MBP and MBP RNA scope. MBP protein and RNA intensity were normalized to mean value. MBP positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p** < 0.01, n = 3 animals. Scale bar = 200 μm. B Immunostaining for MBP and NFH SMI32 and analysis of myelinating and non-myelinating oligodendrocytes in P7 CC. Myelinating and non-myelinating cells were shown in the percentage of total MBP positive cells. Mean ± SD. Student’s Unpaired t test, p**** < 0.0001, n = 3 animals. Scale bar = 100 μm. C P7, P21 and P140 brain section were stained for Olig2 and <t>CC1.</t> Cell number of Olig2 + CC1+ cells were analysed in CC. Data were shown in the percentage of DAPI and Olig2 respectively. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm. D P7 brain section were stained for Ki67, Iba1 and GFAP and proliferation of Ki67+cells was analysed in medial and lateral CC separately. Ki67 positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm.
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Coronal brain sections from Shank3 WT and KO mice of corpus callosum (CC) have been used for all analyses. A Brain sections from P7 WT and Shank3KO mice stained for MBP and MBP RNA scope. MBP protein and RNA intensity were normalized to mean value. MBP positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p** < 0.01, n = 3 animals. Scale bar = 200 μm. B Immunostaining for MBP and NFH SMI32 and analysis of myelinating and non-myelinating oligodendrocytes in P7 CC. Myelinating and non-myelinating cells were shown in the percentage of total MBP positive cells. Mean ± SD. Student’s Unpaired t test, p**** < 0.0001, n = 3 animals. Scale bar = 100 μm. C P7, P21 and P140 brain section were stained for Olig2 and <t>CC1.</t> Cell number of Olig2 + CC1+ cells were analysed in CC. Data were shown in the percentage of DAPI and Olig2 respectively. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm. D P7 brain section were stained for Ki67, Iba1 and GFAP and proliferation of Ki67+cells was analysed in medial and lateral CC separately. Ki67 positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm.
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Coronal brain sections from Shank3 WT and KO mice of corpus callosum (CC) have been used for all analyses. A Brain sections from P7 WT and Shank3KO mice stained for MBP and MBP RNA scope. MBP protein and RNA intensity were normalized to mean value. MBP positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p** < 0.01, n = 3 animals. Scale bar = 200 μm. B Immunostaining for MBP and NFH SMI32 and analysis of myelinating and non-myelinating oligodendrocytes in P7 CC. Myelinating and non-myelinating cells were shown in the percentage of total MBP positive cells. Mean ± SD. Student’s Unpaired t test, p**** < 0.0001, n = 3 animals. Scale bar = 100 μm. C P7, P21 and P140 brain section were stained for Olig2 and <t>CC1.</t> Cell number of Olig2 + CC1+ cells were analysed in CC. Data were shown in the percentage of DAPI and Olig2 respectively. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm. D P7 brain section were stained for Ki67, Iba1 and GFAP and proliferation of Ki67+cells was analysed in medial and lateral CC separately. Ki67 positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm.
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Coronal brain sections from Shank3 WT and KO mice of corpus callosum (CC) have been used for all analyses. A Brain sections from P7 WT and Shank3KO mice stained for MBP and MBP RNA scope. MBP protein and RNA intensity were normalized to mean value. MBP positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p** < 0.01, n = 3 animals. Scale bar = 200 μm. B Immunostaining for MBP and NFH SMI32 and analysis of myelinating and non-myelinating oligodendrocytes in P7 CC. Myelinating and non-myelinating cells were shown in the percentage of total MBP positive cells. Mean ± SD. Student’s Unpaired t test, p**** < 0.0001, n = 3 animals. Scale bar = 100 μm. C P7, P21 and P140 brain section were stained for Olig2 and CC1. Cell number of Olig2 + CC1+ cells were analysed in CC. Data were shown in the percentage of DAPI and Olig2 respectively. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm. D P7 brain section were stained for Ki67, Iba1 and GFAP and proliferation of Ki67+cells was analysed in medial and lateral CC separately. Ki67 positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm.

Journal: Molecular Psychiatry

Article Title: Shank3 related oligodendrocyte alterations in autism are restored by Erk pathway inhibition

doi: 10.1038/s41380-025-03333-1

Figure Lengend Snippet: Coronal brain sections from Shank3 WT and KO mice of corpus callosum (CC) have been used for all analyses. A Brain sections from P7 WT and Shank3KO mice stained for MBP and MBP RNA scope. MBP protein and RNA intensity were normalized to mean value. MBP positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p** < 0.01, n = 3 animals. Scale bar = 200 μm. B Immunostaining for MBP and NFH SMI32 and analysis of myelinating and non-myelinating oligodendrocytes in P7 CC. Myelinating and non-myelinating cells were shown in the percentage of total MBP positive cells. Mean ± SD. Student’s Unpaired t test, p**** < 0.0001, n = 3 animals. Scale bar = 100 μm. C P7, P21 and P140 brain section were stained for Olig2 and CC1. Cell number of Olig2 + CC1+ cells were analysed in CC. Data were shown in the percentage of DAPI and Olig2 respectively. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm. D P7 brain section were stained for Ki67, Iba1 and GFAP and proliferation of Ki67+cells was analysed in medial and lateral CC separately. Ki67 positive cells were shown in the percentage of DAPI. Mean ± SD. Student’s Unpaired t test, p* < 0.05, n = 3 animals. Scale bar = 20 μm.

Article Snippet: CC1 (ms) , Merck , Germany , MABC200 , IHC , 1:500 , 10% DS + 5% FBS + 0.3% Triton in PBS-/-.

Techniques: Staining, RNAscope, Immunostaining