Home LiteratureArticle Details
PMID: 7625610 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Early stages of chick somite development.

Anatomy and embryology ·Vol. 191 ·No. 5 ·1995-05-00 ·Pages 381-96

Christ B, Ordahl CP

Abstract

We report on the formation and early differentiation of the somites in the avian embryo. The somites are derived from the avian embryo. The somites are derived from the mesoderm which, in the body (excluding the head), is subdivided into four compartments: the axial, paraxial, intermediate and lateral plate mesoderm. Somites develop from the paraxial mesoderm and constitute the segmental pattern of the body. They are formed in pairs by epithelialization, first at the cranial end of the paraxial mesoderm, proceeding caudally, while new mesenchyme cells enter the paraxial mesoderm as a consequence of gastrulation. After their formation, which depends upon cell-cell and cell-matrix interactions, the somites impose segmental pattern upon peripheral nerves and vascular primordia. The newly formed somite consists of an epithelial ball of columnar cells enveloping mesenchymal cells within a central cavity, the somitocoel. Each somite is surrounded by extracellular matrix material connecting the somite with adjacent structures. The competence to form skeletal muscle is a unique property of the somites and becomes realized during compartmentalization, under control of signals emanating from surrounding tissues. Compartmentalization is accompanied by altered patterns of expression of Pax genes within the somite. These are believed to be involved in the specification of somite cell lineages. Somites are also regionally specified, giving rise to particular skeletal structures at different axial levels. This axial specification appears to be reflected in Hox gene expression. MyoD is first expressed in the dorsomedial quadrant of the still epithelial somite whose cells are not yet definitely committed. During early maturation, the ventral wall of the somite undergoes an epithelio-mesenchymal transition forming the sclerotome. The sclerotome later becomes subdivided into rostral and caudal halves which are separated laterally by von Ebner's fissure. The lateral part of the caudal half of the sclerotome mainly forms the ribs, neural arches and pedicles of vertebrae, whereas within the lateral part of the rostral half the spinal nerve develops. The medially migrating sclerotomal cells form the peri-notochordal sheath, and later give rise to the vertebral bodies and intervertebral discs. The somitocoel cells also contribute to the sclerotome. The dorsal half of the somite remains epithelial and is referred to as the dermomyotome because it gives rise to the dermis of the back and the skeletal musculature. the cells located within the lateral half of the dermomyotome are the precursors of the muscles of the hypaxial domain of the body, whereas those in the medial half are precursors of the epaxial (back) muscles.(ABSTRACT TRUNCATED AT 400 WORDS)

Related Genes
MeSH Terms
Animals Cell Differentiation Chick Embryo/cytology,growth & development Gene Expression Regulation, Developmental Mesoderm/cytology Muscle, Skeletal/cytology,embryology Spine/embryology
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Christ B
Institute of Anatomy, University of Freiburg, Germany.
Ordahl C P
References (109)
109 references, click to expand
  1. Two myogenic lineages within the developing somite.
    Development. 1992 Feb;114(2):339-53 PMID: 1591996
  2. THE DEVELOPMENT OF SOMITES IN THE CHICK EMBRYO.
    J Embryol Exp Morphol. 1963 Dec;11:697-714 PMID: 14081990
  3. The role of the neural tube and notochord in development of the axial skeleton of the chick.
    Am J Anat. 1954 Nov;95(3):337-99 PMID: 14349892
  4. A series of normal stages in the development of the chick embryo.
    J Morphol. 1951 Jan;88(1):49-92 PMID: 24539719
  5. Regulation of Pax-3 expression in the dermomyotome and its role in muscle development.
    Development. 1994 Apr;120(4):957-71 PMID: 7600971
  6. [Details of the interphase nucleus in Japanese quail (Coturnix coturnix japonica)].
    Bull Biol Fr Belg. 1969;103(3):435-52 PMID: 4191116
  7. The role of extracellular matrix in the formation of the sclerotome.
    J Embryol Exp Morphol. 1979 Dec;54:75-98 PMID: 528873
  8. The contribution made by a single somite to the vertebral column: experimental evidence in support of resegmentation using the chick-quail chimaera model.
    Development. 1988 May;103(1):69-85 PMID: 3197634
  9. The triple origin of skull in higher vertebrates: a study in quail-chick chimeras.
    Development. 1993 Feb;117(2):409-29 PMID: 8330517
  10. [Experimental analysis of somitogenesis in the chick embryo].
    Z Anat Entwicklungsgesch. 1972;138(1):82-97 PMID: 4638678
  11. Myogenic specification in somites: induction by axial structures.
    Development. 1994 Jun;120(6):1443-52 PMID: 8050355
  12. On the origin and development of the ventrolateral abdominal muscles in the avian embryo. An experimental and ultrastructural study.
    Anat Embryol (Berl). 1983;166(1):87-101 PMID: 6220621
  13. Specification and segmentation of the paraxial mesoderm.
    Anat Embryol (Berl). 1994 Apr;189(4):275-305 PMID: 8074321
  14. [Origin of wing musculature. Experimental studies on quail and chick embryos].
    Experientia. 1974 Dec 15;30(12):1446-9 PMID: 4442547
  15. Somitomeres: mesodermal segments of vertebrate embryos.
    Development. 1988;104 Suppl:209-20 PMID: 3077109
  16. An increase in cell-cell adhesion in the chick segmental plate results in a meristic pattern.
    J Embryol Exp Morphol. 1984 Feb;79:1-10 PMID: 6716038
  17. The somitic level of origin of embryonic chick hindlimb muscles.
    Dev Biol. 1988 Apr;126(2):394-407 PMID: 2450796
  18. The mechanism of somite segmentation in the chick embryo.
    J Embryol Exp Morphol. 1979 Jun;51:227-43 PMID: 479747
  19. T-cadherin expression alternates with migrating neural crest cells in the trunk of the avian embryo.
    Development. 1991 Jan;111(1):15-22 PMID: 1707785
  20. Migratory and organogenetic capacities of muscle cells in bird embryos.
    Wilehm Roux Arch Dev Biol. 1980 Jun;189(2):123-134 PMID: 28304961
  21. Site-restricted expression of cytotactin during development of the chicken embryo.
    J Cell Biol. 1986 May;102(5):1917-30 PMID: 2422181
  22. Pax-3 is required for the development of limb muscles: a possible role for the migration of dermomyotomal muscle progenitor cells.
    Development. 1994 Mar;120(3):603-12 PMID: 8162858
  23. Chondrogenesis of the somitic mesoderm.
    Adv Anat Embryol Cell Biol. 1977;53(4):3-47 PMID: 337766
  24. The contribution made by cells from a single somite to tissues within a body segment and assessment of their integration with similar cells from adjacent segments.
    Development. 1989 Dec;107(4):931-43 PMID: 2632241
  25. Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid.
    Cell. 1991 Oct 4;67(1):89-104 PMID: 1680565
  26. A role for Pax-1 as a mediator of notochordal signals during the dorsoventral specification of vertebrae.
    Development. 1993 Nov;119(3):649-60 PMID: 8187635
  27. Early regionalization of somitic mesoderm as studied by the development of axial skeleton of the chick embryo.
    Dev Biol. 1972 May;28(1):142-61 PMID: 5041191
  28. Experimental analysis of the origin of the wing musculature in avian embryos.
    Anat Embryol (Berl). 1977 Mar 30;150(2):171-86 PMID: 857700
  29. Analysis of the in vivo myogenic status of chick somites by desmin expression in vitro.
    Dev Dyn. 1994 Apr;199(4):268-79 PMID: 8075431
  30. Differentiation of chick embryo somites in chorioallantoic culture.
    J Embryol Exp Morphol. 1972 Feb;27(1):215-28 PMID: 5021250
  31. Chondrogenesis in chick embryo somites grafted with adjacent and heterologous tissues.
    J Embryol Exp Morphol. 1972 Feb;27(1):229-34 PMID: 4259876
  32. Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin.
    Development. 1993 Dec;119(4):1079-91 PMID: 8306876
  33. On the origin of cells determined to form skeletal muscle in avian embryos.
    Anat Embryol (Berl). 1988;179(1):49-54 PMID: 3213955
  34. Myogenesis in chick embryo somites in vitro.
    J Embryol Exp Morphol. 1969 Apr;21(2):341-6 PMID: 5822890
  35. The fate of somitocoele cells in avian embryos.
    Anat Embryol (Berl). 1994 Sep;190(3):243-50 PMID: 7529466
  36. On the migration of myogenic stem cells into the prospective wing region of chick embryos. A scanning and transmission electron microscope study.
    Anat Embryol (Berl). 1978 Jun 2;153(2):179-93 PMID: 677470
  37. Differentiation of myoblasts and the relationship between somites and the wing bud of the chick embryo.
    Z Anat Entwicklungsgesch. 1970;132(3):260-71 PMID: 5490539
  38. Adhesion molecules during somitogenesis in the avian embryo.
    J Cell Biol. 1987 May;104(5):1361-74 PMID: 3553211
  39. An experimental analysis of the developmental capacities of distal parts of avian leg buds.
    Am J Anat. 1985 Aug;173(4):321-40 PMID: 20726129
  40. From somites to vertebral column.
    Ann Anat. 1992 Feb;174(1):23-32 PMID: 1605355
  41. Asymmetric expression in somites of cytotactin and its proteoglycan ligand is correlated with neural crest cell distribution.
    Proc Natl Acad Sci U S A. 1987 Nov;84(22):7977-81 PMID: 2446315
  42. [Experimental studies on the development of the thoracic wall in chick embryos].
    Experientia. 1974 Dec 15;30(12):1449-51 PMID: 4140791
  43. Ontogeny of avian extrinsic ocular muscles. I. A light- and electron-microscopic study.
    Cell Tissue Res. 1984;237(3):549-57 PMID: 6386166
  44. The role of fibronectin and laminin in development and migration of the avian Wolffian duct with reference to somitogenesis.
    Anat Embryol (Berl). 1991;183(4):385-95 PMID: 1867390
  45. Aspects of spinal cord induction of chondrogenesis in chick embryo somites.
    J Embryol Exp Morphol. 1972 Feb;27(1):235-43 PMID: 4336558
  46. The migration of myogenic cells from the somites into the leg region of avian embryos. An ultrastructural study.
    Anat Embryol (Berl). 1979;157(3):291-309 PMID: 525819
  47. Signals from the notochord and floor plate regulate the region-specific expression of two Pax genes in the developing spinal cord.
    Development. 1993 Mar;117(3):1001-16 PMID: 8100762
  48. Pathways and mechanisms of avian trunk neural crest cell migration and localization.
    Dev Biol. 1982 Oct;93(2):324-43 PMID: 7141101
  49. Cell contacts and rearrangements preceding somitogenesis in chick embryo.
    Cell Differ. 1983 Apr;12(4):191-204 PMID: 6839361
  50. Respecification of vertebral identities by retinoic acid.
    Development. 1992 Jun;115(2):487-501 PMID: 1358593
  51. Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity.
    Cell. 1993 Dec 31;75(7):1417-30 PMID: 7916661
  52. Cell junctions in the early chick embryo--a freeze etch study.
    Dev Biol. 1973 Dec;35(2):302-17 PMID: 4788223
  53. Light microscope observations on actin distribution during morphogenetic movements in the chick embryo.
    J Embryol Exp Morphol. 1983 Dec;78:23-32 PMID: 6663227
  54. Local signalling in dermomyotomal cell type specification.
    Anat Embryol (Berl). 1992 Oct;186(5):505-10 PMID: 1443658
  55. Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos.
    Anat Embryol (Berl). 1995 Apr;191(4):297-310 PMID: 7645756
  56. The Splotch mutation interferes with muscle development in the limbs.
    Anat Embryol (Berl). 1993 Feb;187(2):153-60 PMID: 8238963
  57. The formation of premuscle masses during chick wing bud development.
    Anat Embryol (Berl). 1990;182(3):235-47 PMID: 2268067
  58. Mechanisms of vertebrate segmentation.
    Development. 1988 Jul;103(3):413-29 PMID: 3073078
  59. On the determination of mesodermal tissues in the avian embryonic wing bud.
    Anat Embryol (Berl). 1981;161(3):283-9 PMID: 7187823
  60. [Is there a spatial relationship between the level of origin of somitic myogenic cells and their terminal site in the wing? (author's transl)].
    Arch Anat Microsc Morphol Exp. 1980;69(1):35-46 PMID: 7458319
  61. Variations of cervical vertebrae after expression of a Hox-1.1 transgene in mice.
    Cell. 1990 Apr 20;61(2):301-8 PMID: 1970515
  62. Molecular differences between the rostral and caudal halves of the sclerotome in the chick embryo.
    Development. 1989 Mar;105(3):541-8 PMID: 2612364
  63. The contribution of the primitive streak to the somites in the avian embryo.
    J Embryol Exp Morphol. 1986 Mar;92:193-206 PMID: 3723062
  64. Analysis of the early stages of trunk neural crest migration in avian embryos using monoclonal antibody HNK-1.
    Dev Biol. 1986 May;115(1):44-55 PMID: 3516760
  65. The migration of neural crest cells and the growth of motor axons through the rostral half of the chick somite.
    J Embryol Exp Morphol. 1985 Dec;90:437-55 PMID: 3834038
  66. Differentiating abilities of avian somatopleural mesoderm.
    Experientia. 1979 Oct 15;35(10):1376-8 PMID: 499431
  67. Chick somite determination: the role of factors in young somites and the segmental plate.
    J Exp Zool. 1978 Feb;203(2):295-306 PMID: 624929
  68. Analysis of normal somite development.
    Dev Biol. 1974 May;38(1):73-90 PMID: 4826295
  69. Limb-somite relationship: origin of the limb musculature.
    J Embryol Exp Morphol. 1977 Oct;41:245-58 PMID: 591873
  70. Early expression of the myogenic regulatory gene, myf-5, in precursor cells of skeletal muscle in the mouse embryo.
    Development. 1991 Apr;111(4):1097-107 PMID: 1652425
  71. Neural crest cells prefer the myotome's basal lamina over the sclerotome as a substratum.
    Dev Biol. 1994 Jun;163(2):389-406 PMID: 7515361
  72. Chondrogenesis in chick embryo somites in vitro.
    J Embryol Exp Morphol. 1969 Apr;21(2):331-40 PMID: 5387792
  73. [An autoradiographic study of the presumptive fate of the primitive streak in chick embryos].
    J Embryol Exp Morphol. 1970 Feb;23(1):70-108 PMID: 5511825
  74. Fate mapping and cell lineage analysis of Hensen's node in the chick embryo.
    Development. 1991 Jun;112(2):615-26 PMID: 1794328
  75. Sonic hedgehog mediates the polarizing activity of the ZPA.
    Cell. 1993 Dec 31;75(7):1401-16 PMID: 8269518
  76. The migration of myogenic cells from the somites at the wing level in avian embryos.
    Dev Biol. 1987 Jun;121(2):389-96 PMID: 3556267
  77. Segmentation in the vertebrate nervous system.
    Nature. 1984 Aug 30-Sep 5;310(5980):786-9 PMID: 6472458
  78. Interactions between neurites and somite cells: inhibition and stimulation of nerve growth in the chick embryo.
    J Embryol Exp Morphol. 1986 Feb;91:209-26 PMID: 3519826
  79. Mesoderm movement and fate during avian gastrulation and neurulation.
    Dev Dyn. 1992 Mar;193(3):235-48 PMID: 1600242
  80. Maturation of myogenic and chondrogenic cells in the presomitic mesoderm of the chick embryo.
    Exp Cell Res. 1994 Apr;211(2):263-74 PMID: 8143772
  81. Sequential activation of three myogenic regulatory genes during somite morphogenesis in quail embryos.
    Dev Biol. 1992 May;151(1):67-79 PMID: 1315698
  82. Autonomy of differentiation in avian branchial somites and the influence of adjacent tissues.
    Development. 1987 Jul;100(3):449-62 PMID: 3308405
  83. Grafting experiments on determination and migratory behaviour of presomitic, somitic and somatopleural cells in avian embryos.
    Anat Embryol (Berl). 1982;164(3):369-78 PMID: 7137584
  84. Determination of somite cells: independence of cell differentiation and morphogenesis.
    Development. 1988 Sep;104(1):15-28 PMID: 3253056
  85. The development of the vertebral column.
    Adv Anat Embryol Cell Biol. 1985;90:1-122 PMID: 3969844
  86. Alpha actinin distribution and extracellular matrix products during somitogenesis and neurulation in the chick embryo.
    Cell Motil. 1985;5(6):491-506 PMID: 3907849
  87. Pair-rule gene expression in the somitic stage chick embryo: association with somite segmentation and border formation.
    Differentiation. 1993 Sep;54(2):73-83 PMID: 8243893
  88. Communication compartments in the axial mesoderm of the chick embryo.
    Anat Embryol (Berl). 1992 Jul;186(2):195-204 PMID: 1510249
  89. [Regional determination of the paraxial mesoderm in young chick embryos].
    Verh Anat Ges. 1975;69:263-9 PMID: 1229288
  90. Origins and patterning of avian outflow tract endocardium.
    Development. 1991 Apr;111(4):867-76 PMID: 1879358
  91. Development of the chick embryo mesoblast. Formation of the embryonic axis and establishment of the metameric pattern.
    Dev Biol. 1979 Nov;73(1):24-45 PMID: 527768
  92. An experimental analysis of the development of the spinal column. VI. Aspects of cartilage induction.
    Exp Cell Res. 1957 Oct;13(2):292-303 PMID: 13480296
  93. [The early differentiation of the perinotochordal connective tissue. A scanning and transmission electron microscopic study on chick embryos (author's transl)].
    Experientia. 1975 Sep 15;31(9):1083-6 PMID: 1175754
  94. The immediate fate of cells in the epithelial somite of the chick embryo.
    Anat Embryol (Berl). 1993 Nov;188(5):441-7 PMID: 8311251
  95. The extrinsic ocular muscles in birds are derived from the prechordal plate.
    Naturwissenschaften. 1984 Jul;71(7):379-80 PMID: 6482980
  96. Peanut agglutinin and chondroitin-6-sulfate are molecular markers for tissues that act as barriers to axon advance in the avian embryo.
    Dev Biol. 1991 Sep;147(1):187-206 PMID: 1908800
  97. [The histogenesis of somites in the chick].
    J Embryol Exp Morphol. 1976 Dec;36(3):669-83 PMID: 1010985
  98. The distribution of tenascin coincides with pathways of neural crest cell migration.
    Development. 1988 Jan;102(1):237-50 PMID: 2458221
  99. On the role of fibronectin during the compaction stage of somitogenesis in the chick embryo.
    J Exp Zool. 1984 Nov;232(2):197-206 PMID: 6389752
  100. Control of dorsoventral patterning of somitic derivatives by notochord and floor plate.
    Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5242-6 PMID: 8506372
  101. A radioautographic study of the development of the somite in the chick embryo.
    J Embryol Exp Morphol. 1968 Apr;19(2):217-26 PMID: 5656455
  102. Pax-3 expression in segmental mesoderm marks early stages in myogenic cell specification.
    Development. 1994 Apr;120(4):785-96 PMID: 7600957
  103. The influence of axial structures on chick somite formation.
    Dev Biol. 1976 Oct 1;53(1):36-48 PMID: 976598
  104. The onset of myotome formation in the chick.
    Anat Embryol (Berl). 1988;177(3):191-201 PMID: 2451450
  105. Two molecules related to the VEGF receptor are expressed in early endothelial cells during avian embryonic development.
    Mech Dev. 1993 Jul;42(1-2):33-48 PMID: 8396413
  106. The ventralizing effect of the notochord on somite differentiation in chick embryos.
    Anat Embryol (Berl). 1993 Sep;188(3):239-45 PMID: 8250279
  107. Early mesoderm differentiation in the chick embryo.
    Anat Embryol (Berl). 1991;183(2):143-9 PMID: 2035850
  108. Emergence of myogenic and endothelial cell lineages in avian embryos.
    Dev Biol. 1994 May;163(1):270-8 PMID: 8174781
  109. The early migration of neural crest cells in the trunk region of the avian embryo: an electron microscopic study.
    Dev Biol. 1978 Feb;62(2):317-33 PMID: 627310
Article Info
Journal
Anatomy and embryology
Abbr.
Anat Embryol (Berl)
ISSN
0340-2061
Published
1995-05-00
Pages
381-96
Language
English
Region
Germany
NLM ID
7505194
Subset
IM
Grants
NHLBI NIH HHS · HL43821 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com