Spatial rearrangement of Purkinje cell subsets forms the transverse and longitudinal compartmentalization in the mouse embryonic cerebellum

Transversely oriented lobules and longitudinally arrayed stripes of Purkinje cell subsets subdivide the cerebellar cortex into multiple compartments that are involved in diverse functions. In the mammalian cerebellum, anterior, and posterior lobules, which are involved in somatosensorimotor function...

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Veröffentlicht in:Journal of comparative neurology (1911) 2017-10, Vol.525 (14), p.2971-2990
Hauptverfasser: Vibulyaseck, Suteera, Fujita, Hirofumi, Luo, Yuanjun, Tran, Anh Khoa, Oh‐Nishi, Arata, Ono, Yuichi, Hirano, Shinji, Sugihara, Izumi
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container_issue 14
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container_title Journal of comparative neurology (1911)
container_volume 525
creator Vibulyaseck, Suteera
Fujita, Hirofumi
Luo, Yuanjun
Tran, Anh Khoa
Oh‐Nishi, Arata
Ono, Yuichi
Hirano, Shinji
Sugihara, Izumi
description Transversely oriented lobules and longitudinally arrayed stripes of Purkinje cell subsets subdivide the cerebellar cortex into multiple compartments that are involved in diverse functions. In the mammalian cerebellum, anterior, and posterior lobules, which are involved in somatosensorimotor function, show an alternation of aldolase C (zebrin II) ‐positive and ‐negative stripes, whereas the central lobules (lobules VIb–VII and crus I), which are implicated in nonmotor functions, show a laterally expanded arrangement solely of aldolase C‐positive stripes. To understand the developmental process of this compartmental pattern, we identified groups of Purkinje cell subsets in the entire mouse cerebellum at embryonic day (E) 14.5 by staining Purkinje cell subset markers. We then tracked four major domains of Protocadherin 10 (Pcdh10)‐positive Purkinje cell subsets (medial, dorsal, central, and mid‐lateral subsets), which were clearly demarcated during E14.5–17.5. These domains of Purkinje cell subsets shifted predominantly in the longitudinal direction to be positioned in the anterior and posterior lobules. However, a particular portion of the medial and mid‐lateral domains, and the whole of the central domain shift in the lateral direction to be positioned in the central lobules. The results indicate that while the longitudinal shift of domains of Purkinje cell subsets forms the longitudinally striped compartments in the anterior and posterior cerebellum, the lateral shift of particular domains of Purkinje cell subsets underlies the laterally expanded arrangement of stripes in central lobules. Thus, the rearrangement of Purkinje cell subsets in the embryonic cerebellum is critically related to the compartmental organization in the mammalian cerebellum. The authors clarified three‐dimensional distribution of Protocadherin 10‐positive Purkinje cell subsets in the mouse cerebellum at embryonic day (E) 14.5 and tracked them from E14.5 to E17.5. The revealed rearrangement processes of Purkinje cell subsets show how the cerebellar compartmentalization is formed in the central cerebellar lobules.
doi_str_mv 10.1002/cne.24250
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In the mammalian cerebellum, anterior, and posterior lobules, which are involved in somatosensorimotor function, show an alternation of aldolase C (zebrin II) ‐positive and ‐negative stripes, whereas the central lobules (lobules VIb–VII and crus I), which are implicated in nonmotor functions, show a laterally expanded arrangement solely of aldolase C‐positive stripes. To understand the developmental process of this compartmental pattern, we identified groups of Purkinje cell subsets in the entire mouse cerebellum at embryonic day (E) 14.5 by staining Purkinje cell subset markers. We then tracked four major domains of Protocadherin 10 (Pcdh10)‐positive Purkinje cell subsets (medial, dorsal, central, and mid‐lateral subsets), which were clearly demarcated during E14.5–17.5. These domains of Purkinje cell subsets shifted predominantly in the longitudinal direction to be positioned in the anterior and posterior lobules. However, a particular portion of the medial and mid‐lateral domains, and the whole of the central domain shift in the lateral direction to be positioned in the central lobules. The results indicate that while the longitudinal shift of domains of Purkinje cell subsets forms the longitudinally striped compartments in the anterior and posterior cerebellum, the lateral shift of particular domains of Purkinje cell subsets underlies the laterally expanded arrangement of stripes in central lobules. Thus, the rearrangement of Purkinje cell subsets in the embryonic cerebellum is critically related to the compartmental organization in the mammalian cerebellum. The authors clarified three‐dimensional distribution of Protocadherin 10‐positive Purkinje cell subsets in the mouse cerebellum at embryonic day (E) 14.5 and tracked them from E14.5 to E17.5. 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In the mammalian cerebellum, anterior, and posterior lobules, which are involved in somatosensorimotor function, show an alternation of aldolase C (zebrin II) ‐positive and ‐negative stripes, whereas the central lobules (lobules VIb–VII and crus I), which are implicated in nonmotor functions, show a laterally expanded arrangement solely of aldolase C‐positive stripes. To understand the developmental process of this compartmental pattern, we identified groups of Purkinje cell subsets in the entire mouse cerebellum at embryonic day (E) 14.5 by staining Purkinje cell subset markers. We then tracked four major domains of Protocadherin 10 (Pcdh10)‐positive Purkinje cell subsets (medial, dorsal, central, and mid‐lateral subsets), which were clearly demarcated during E14.5–17.5. These domains of Purkinje cell subsets shifted predominantly in the longitudinal direction to be positioned in the anterior and posterior lobules. However, a particular portion of the medial and mid‐lateral domains, and the whole of the central domain shift in the lateral direction to be positioned in the central lobules. The results indicate that while the longitudinal shift of domains of Purkinje cell subsets forms the longitudinally striped compartments in the anterior and posterior cerebellum, the lateral shift of particular domains of Purkinje cell subsets underlies the laterally expanded arrangement of stripes in central lobules. Thus, the rearrangement of Purkinje cell subsets in the embryonic cerebellum is critically related to the compartmental organization in the mammalian cerebellum. The authors clarified three‐dimensional distribution of Protocadherin 10‐positive Purkinje cell subsets in the mouse cerebellum at embryonic day (E) 14.5 and tracked them from E14.5 to E17.5. 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In the mammalian cerebellum, anterior, and posterior lobules, which are involved in somatosensorimotor function, show an alternation of aldolase C (zebrin II) ‐positive and ‐negative stripes, whereas the central lobules (lobules VIb–VII and crus I), which are implicated in nonmotor functions, show a laterally expanded arrangement solely of aldolase C‐positive stripes. To understand the developmental process of this compartmental pattern, we identified groups of Purkinje cell subsets in the entire mouse cerebellum at embryonic day (E) 14.5 by staining Purkinje cell subset markers. We then tracked four major domains of Protocadherin 10 (Pcdh10)‐positive Purkinje cell subsets (medial, dorsal, central, and mid‐lateral subsets), which were clearly demarcated during E14.5–17.5. These domains of Purkinje cell subsets shifted predominantly in the longitudinal direction to be positioned in the anterior and posterior lobules. However, a particular portion of the medial and mid‐lateral domains, and the whole of the central domain shift in the lateral direction to be positioned in the central lobules. The results indicate that while the longitudinal shift of domains of Purkinje cell subsets forms the longitudinally striped compartments in the anterior and posterior cerebellum, the lateral shift of particular domains of Purkinje cell subsets underlies the laterally expanded arrangement of stripes in central lobules. Thus, the rearrangement of Purkinje cell subsets in the embryonic cerebellum is critically related to the compartmental organization in the mammalian cerebellum. The authors clarified three‐dimensional distribution of Protocadherin 10‐positive Purkinje cell subsets in the mouse cerebellum at embryonic day (E) 14.5 and tracked them from E14.5 to E17.5. The revealed rearrangement processes of Purkinje cell subsets show how the cerebellar compartmentalization is formed in the central cerebellar lobules.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28542916</pmid><doi>10.1002/cne.24250</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0001-9630-2756</orcidid><orcidid>https://orcid.org/0000-0002-4598-9882</orcidid></addata></record>
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ispartof Journal of comparative neurology (1911), 2017-10, Vol.525 (14), p.2971-2990
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language eng
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Aldolase
Animals
Cadherins - genetics
Cadherins - metabolism
Cell Movement
Cerebellar Cortex - cytology
Cerebellar Cortex - embryology
Cerebellar Cortex - metabolism
cerebellar development
cerebellar lobules
Cerebellum
Compartments
Corl2
Embryos
Forkhead Transcription Factors - metabolism
Imaging, Three-Dimensional
Immunohistochemistry
Mice, Inbred C3H
Mice, Inbred C57BL
Mice, Transgenic
Microscopy, Fluorescence
Nuclear Receptor Subfamily 1, Group F, Member 1 - metabolism
Protocadherin
Protocadherin 10
Purkinje cells
Purkinje Cells - cytology
Purkinje Cells - metabolism
Receptor, EphA4 - metabolism
Repressor Proteins - metabolism
RRID:AB_10015300
RRID:AB_10807416
RRID:AB_10818782
RRID:AB_2107112
RRID:AB_2180141
RRID:AB_2313606
RRID:AB_2340401
Staining
Zebrin II
title Spatial rearrangement of Purkinje cell subsets forms the transverse and longitudinal compartmentalization in the mouse embryonic cerebellum
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