Identification of an early subset of cerebellar nuclei neurons in mice
- Department of Human Anatomy and Cell Science, The Children's Hospital Research Institute of Manitoba (CHRIM), Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Canada
- Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, University of British Columbia, Canada
- Department of Pharmacology and Therapeutics, Division of Neurodegenerative Disorders, St Boniface Hospital Albrechtsen Research Centre, University of Manitoba, Canada
- Université Côte d’Azur, CNRS, Inserm, iBV, France
- University of California, San Francisco (UCSF), United States
- Department of Neuroscience, Baylor College of Medicine, United States
- Jan and Dan Duncan Neurological Research Institute at Texas Children’s Hospital, United States
- Howard Hughes Medical Institute, Baylor College of Medicine, United States
- Division of Neuroscience, IRCCS Ospedale San Raffaele, Italy
- Università Vita-Salute San Raffaele, Italy
Figures
Figure 1
The presence of neurons in the cerebellar primordium at embryonic day (E)9 and spatial expression of SNCA.
The cerebellar primordium immunostained with neurofilament-associated antigens (NAA) and SNCA shows that a distinct subset of neurons located at the rostral end of the developing cerebellum. (A) Dorsal view of the schematic illustration of the cerebellar primordium, mesencephalon, isthmus, and 4th ventricle. The red line indicates the sagittal plane about which the sections shown in (B–D) were taken. (B–D) Sagittal section through the cerebellar primordium at early E9 immunoperoxidase-labeled with NAA 3A10 shows the presence of neurons in the cerebellar primordium that cross the isthmus (i) and continue to the mesencephalon. (C) A higher magnification of (B). (D) Differentiated neurons at E9.5 are visible; a higher magnification is shown in the inset, d. (E) Sagittal section through the cerebellar primordium at late E9. Immunofluorescence labeling of SNCA shows SNCA+ (green) expressing CN neurons in the mesencephalon, at the isthmus (i) and in the rostral part of the cerebellar primordium (cb). (F) A higher magnification of (E). Abbreviations: 4thv, 4th ventricle; cb, cerebellum; c, caudal; d, dorsal; i, isthmus; m, mesencephalon; r, rostral; v, ventral. Scale bar = 100 µm in (B); 50 µm in (C and E); 20 µm in (D).
Figure 2
SNCA expression relative to Lmx1a in the early developing mouse cerebellum.
The sagittal section through the cerebellar primordium at embryonic day (E)12.5 reveals double immunofluorescence labeling with SNCA and LMX1A antibodies in both medial (A–D) and lateral (E–H) sections.
(A–G) SNCA (green, A and E) and LMX1A (red, B and F) immunopositive cells are located at the NTZ. SNCA+ cells continue to the mesencephalon, and LMX1A+ cells toward the rhombic lip. Merged images show that the SNCA+ cells form a population of cerebellar nuclei (CN) neurons distinct from the rhombic lip-derived cells (LMX1A+) in the NTZ (C and G). (D and H) show a higher magnification of (C and G), respectively. Abbreviations: 4thV, 4th ventricle; cb, cerebellum; c, caudal; d, dorsal; i, isthmus; m, mesencephalon; rl, rhombic lip; NTZ, nuclear transitory zone; r, rostral; v, ventral. Scale bar = 100 µm.
Figure 3 with 1 supplement
Expression of SNCA and OTX2 in the developing cerebellar primordium.
Double immunofluorescence labeling with SNCA and OTX2 antibodies in sagittal sections of the cerebellar primordium at embryonic day (E)12.5. (A–E) Double immunolabeling of SNCA (green) and OTX2 (red) of a sagittal section of the cerebellar primordium at E12.5. (A) High OTX2 immunoreactivity was detected in the mesencephalon. SNCA+ cells in the mesencephalon accompany OTX2+ cells across the isthmus (i) and in the NTZ. (B) Higher magnification of (A). (C–E) Immunolabeling with SNCA (green, C) and OTX2 (red, D) and merged (E) shows co-expression in the NTZ. (F–G) Cerebellar cells at E12 and E14 were dissociated and immunolabeled for SNCA+OTX2, SNCA+LMX1A, or each antibody individually (F). Quantitative analysis was performed by flow cytometry to detect SNCA+, OTX2+, LMX1A+, SNCA+/ LMX1A+, and SNCA+/OTX2+ cells (G). No significant differences were observed for the number of LMX1A+ cells between E12 and E14. An increase in SNCA- and OTX2-positive cells was shown at E14 in comparison to E12 (*p<0.05). The number of cells positive for SNCA/LMX1A or SNCA/OTX2 was very low at E12 and E14. Abbreviations: 4thv, 4th ventricle; cb, cerebellum; c, caudal; d, dorsal; i, isthmus; m, mesencephalon; rl, rhombic lip; NTZ, nuclear transitory zone; r, rostral; v, ventral. Scale bar = 200 µm in (A); 50 µm in (B); 20 µm in (C, D and E).
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Figure 3—source data 1
The content of this file is original FACS data for Figure 3F.
- https://cdn.elifesciences.org/articles/93778/elife-93778-fig3-data1-v1.pdf
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Figure 3—source data 2
The content of this file is used for Figure 3G.
- https://cdn.elifesciences.org/articles/93778/elife-93778-fig3-data2-v1.zip
Figure 3—figure supplement 1
OTX2 expression persists in Snca null mice.
OTX2 immunoperoxidase staining in the cerebellar primordium of Pap-/-; Snca-/- mice at embryonic day (E)12. Results show OTX2+ cells are present in the ntz and terminate in the rostral cerebellar primordium. Abbreviations: cb, cerebellum; I, isthmus; ntz, nuclear transitory zone. Scale bar = 50 µm.
Figure 4
The spatial and temporal expression of OTX2 in the developing cerebellum of mice.
Sagittal sections through the cerebellar primordia at E12, E13, E14, and E15 were analyzed for peroxidase immunoreactivity of OTX2. (A–F) Sagittal section through cerebellar primordium at E12 (A; higher magnification shown in B), E13 (C; higher magnification shown in D), E14 (E), and E15 (F). High OTX2 immunoreactivity at the mesencephalon is evident, and a few OTX2+ cells cross the isthmus and position at the rostral part of the cerebellar primordium at the NTZ. Examples of Otx2 expressing cells are indicated by arrowheads in B, D, E, and F. In (E and F), the isthmus and adjacent cerebellar area are shown in the same orientation as (A–D) (I; isthmus). The orientation label (r-c and d-v; rostral caudal and dorsal ventral) in (A) applies to all panels. (G) Comparison of the number of OTX2-positive cells in the cerebellar primordium from E12 to E15. Results indicate a slight increase in the number of OTX2-positive cells over time. Significant differences were observed between E12 and E14 (**p<0.01), E12, and E15 (***p<0.001), as well as E13 and E15 (#p<0.05). Data were analyzed by one-way ANOVA followed by a Tukey’s multiple comparison test. Abbreviations: 4thv, 4th ventricle; cb, cerebellum; c, caudal; d, dorsal; i, isthmus; m, mesencephalon; rl, rhombic lip; r, rostral; v, ventral. Scale bar = 200 µm in (A) and (C); 50 µm in (F) (applies to B, D, E, and F).
Figure 5 with 1 supplement
Otx2 expression in developing cerebella of Otx2-GFP transgenic and control mice.
Sagittal sections through the cerebellar primordium of Otx2-GFP transgenic mice at embryonic day (E)13 are shown in (A–D), and RNAscope fluorescence in situ hybridization (FISH) of Otx2 at E12 in wild-type mice in (E–J). (A–D) DAPI labels the outline of the cerebellar primordium and mesencephalon (A, blue). GFP expression, which is enhanced by immunofluorescence labeling with anti-GFP (B, green), and immunofluorescence labeling for OTX2 (C, red), reveal co-labeled cells (D, merged) in the mesencephalon and NTZ at the rostral end of the cerebellar primordium. Arrows indicate the isthmus. (E–G) Merged channels of the in situ hybridization of Otx2 mRNA probe counterstained with DAPI at low (E) and high (F and G) magnification captured by confocal microscopy. (H–J) The Otx2 mRNA signal was strong in the mesencephalon and extended as a tail through the isthmus to the rostral cerebellar primordium in the NTZ. The isthmus is indicated by arrows in (E, F, H, I) and a line in (J). Abbreviations: cb, cerebellum; c, caudal; d, dorsal; m, mesencephalon; rl, rhombic lip; ntz, nuclear transitory zone; r, rostral; v, ventral. Scale bar = 200 µm in (D) (applies to A–D); 100 µm in (H) (applies to E and H); 20 µm in (J) (applies to F–J).
Figure 5—figure supplement 1
In situ hybridization demonstrates expression pattern of Otx2, Snca, C-Ret, and Tlx3.
These images show distribution of Otx2, Snca, C-Ret, and Tlx3 in the cerebellar primordium at embryonic day (E)11.5, E13.5, and E15.5; all markers are present in the rostroventral region of the nuclear transitory zone (NTZ). All images show cerebellar primordia.
© 2008, Allen Institute for Brain Science. Images are from the Allen Mouse Brain Atlas (https://developingmouse.brain-map.org/), and are not available under the terms of a Creative Commons Attribution License. Further reproductions of these images should adhere to the Allen Institute's Citation policy (https://alleninstitute.org/legal/citation-policy/).
Figure 6
SNCA immunopositive cells express p75NTR (nerve growth factor receptor [NGFR]) in developing cerebellum in vivo and in vitro.
(A–D) Double immunofluorescence labeling with SNCA A, green and p75NTR (B, red) antibodies reveals co-labeled cells (C, merged) in the NTZ; a higher magnification of the NTZ is shown in (D). (d) Western blot analysis of SNCA and p75NTR expression during cerebellar development. Immunoblots of total cerebellar lysates from embryos at E11, E13, and E15 indicate an increase in expression of SNCA and p75NTR from E11 to E15. Equal protein loading was confirmed by β-actin expression. (E–H) Primary dissociated cultures of cerebellum obtained from an E10 mouse embryo (days in vitro [DIV] 4), double immunofluorescence stained for SNCA (E: green) and p75NTR (F: red) (merged image shown in G). (H) is a higher magnification of (G); punctuate cellular p75NTR immunoreactivity is marked by arrow heads. Abbreviations: cb, cerebellum; c, caudal; d, dorsal; NTZ, nuclear transitory zone; r, rostral; v, ventral. Scale bar = 50 µm in (A–C) and (D–F); 20 µm in (H); 10 µm in (G).
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Figure 6—source data 1
This file has the original scan of western blot bands used for Figure 6D.
- https://cdn.elifesciences.org/articles/93778/elife-93778-fig6-data1-v1.tif
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Figure 6—source data 2
The content of this file is showing replicates of western blot finding, supporting Figure 6D.
- https://cdn.elifesciences.org/articles/93778/elife-93778-fig6-data2-v1.zip
Figure 7
SNCA, OTX2, and MEIS2 expression in the developing cerebella of Atoh1 null and control mice.
Sagittal sections through the cerebellar primordia of Atoh1+/+ and Atoh1-/- embryos at embryonic day (E)12.5; double immunofluorescence labeling with SNCA+OTX2 and SNCA+MEIS2 antibodies is demonstrated. (A–C) SNCA (green, A) and OTX2 (red, B) immunopositive cells are present in the mesencephalon and NTZ of Atoh1 KO mouse (merged channels, C).(D–F) In E12.5 Atoh1+/+ sagittal sections, SNCA+ (green, D) cells are observed in the mesencephalon and NTZ. MEIS2+ (red, E) cells are present in the mesencephalon and NTZ in addition to another population of MEIS2+ cells in the dorsal region of the NTZ which extends to the rhombic lip. Merged image (F) confirms the presence of two distinct sets of MEIS2+ cells in the NTZ: rhombic lip-derived CN neurons located in the caudodorsal (cd) region, which do not express SNCA (MEIS2+/SNCA-), and a subset of MEIS2+/SNCA+ CN neurons situated in the rostroventral (rv) region of the NTZ. (G–I) Higher magnification of (D–F). (J–L) In E12.5 Atoh1-/- sagittal sections, the expression of SNCA (green, J) shows no change as compared to Atoh1+/+, whereas Meis2 abundance (red, K) exhibited a different pattern. Thus, MEIS2+/SNCA+ cells were still present in the rostroventral region of the NTZ. However, the subpopulation of MEIS2+/SNCA- rhombic lip-derived CN neurons were absent in the caudodorsal region of the NTZ. (M–O) Higher magnification of (J–I). Abbreviations: 4thV, 4th ventricle; cb, cerebellum; cd, caudodorsal; i, isthmus; m, mesencephalon; rl, rhombic lip; NTZ, nuclear transitory zone; rv, rostroventral. Scale bar = 100 µm.
Figure 8 with 2 supplements
Labeling of mesencephalic cells during early development in mice using embryonic culture.
FAST DiI was applied to an embryo at embryonic day (E)9 and kept for 4 days (days in vitro [DIV] 4, A–C) or removed after 24 hr (DIV 1, D–E). (A, a) FAST DiI was inserted in the mesencephalon at E9 (DIV 0), arrowhead shows insertion location of DiI crystal in the mesencephalon. The arrow indicates the isthmus. Inset ‘a’ shows the whole embryo and indicates the site of DiI insertion. (B–C) 4 days post DiI insertion, DiI-positive cells directed both rostrally to the mesencephalon (B) and caudally to the rostral cerebellar primordium (C). (D, d) FAST DiI was inserted in the mesencephalon at E9 (DIV 0) (indicated by arrowhead) and removed at DIV 1, arrow shows the isthmus. Inset ‘d’ shows the whole embryo and indicates the site of DiI insertion. (E, e) DiI-positive cells present in cerebellar primordium at DIV 6 after removal of FAST DiI at DIV 1. Abbreviations: cb, cerebellum; c, caudal; d, dorsal; m, mesencephalon; r, rostral; v, ventral. Scale bar = 500 µm in (a, d); 200 µm in (A, D); 100 µm in (B–C, E).
Figure 8—figure supplement 1
FAST DiI was applied to an embryo at embryonic day (E9) and kept for 4 days in vitro (DIV 4), revealing labeled cells within the cerebellar primordium.
(A–C) Low and high magnifications show only a few positive cells in the rostral cerebellar primordium in the NTZ at the level of the medial cerebellar section. (D–F) Low and high magnifications indicate the presence of just a few positive cells in the rostral cerebellar primordium in the NTZ at the level of the lateral cerebellar section. Abbreviations: cb, cerebellum; c, caudal; d, dorsal; m, mesencephalon; NTZ, nuclear transitory zone; r, rostral; v, ventral. Scale bar = 100 µm in (A) applies to (D); 50 µm in (B) applies to (E); 20 µm in (C) applies to (I) as well.
Figure 8—figure supplement 2
FAST DiI was applied to the embryo at embryonic day (E)9 and removed after 24 hr, resulting in the visualization of labeled cells within the cerebellar primordium (higher magnification in Figure 8E, e).
(A) DiI-positive cells present in cerebellar primordium at days in vitro (DIV) 6 after removal of FAST DiI at DIV 1 (indicated by arrowhead), arrow points to the isthmus. (B) A higher magnification from the caudal to mesencephalon and rostral rhombencephalon shows DiI-positive cells in the cerebellar primordium, arrow points to the isthmus. Abbreviations: cb, cerebellum; c, caudal; d, dorsal; m, mesencephalon; r, rostral; v, ventral. Scale bar = 500 µm in (B); 100 µm in (C).
Figure 9
A schematic illustration of the developing cerebellum at ~E12 (embryonic day 12), created using BioRender.com.
The expression patterns of SNCA, MEIS2, and OTX2 within the cerebellar primordium indicate a subset of cerebellar nuclei (CN) neurons with origins distinct from the rhombic lip (rl). Abbreviations: c, caudal; d, dorsal; m, mesencephalon; ntz, nuclear transitory zone; r, rostral; rl, rhombic lip; v, ventral.
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Identification of an early subset of cerebellar nuclei neurons in mice
eLife 13:RP93778.
https://doi.org/10.7554/eLife.93778.4
