Cleavage (embryo)

In embryology, cleavage is the division of cells in the early development of the embryo, following fertilization.[1] The zygotes of many species undergo rapid cell cycles with no significant overall growth, producing a cluster of cells the same size as the original zygote. The different cells derived from cleavage are called blastomeres and form a compact mass called the morula. Cleavage ends with the formation of the blastula, or of the blastocyst in mammals.

Depending mostly on the concentration of yolk in the egg, the cleavage can be holoblastic (total or entire cleavage) or meroblastic (partial cleavage). The pole of the egg with the highest concentration of yolk is referred to as the vegetal pole while the opposite is referred to as the animal pole.

Cleavage differs from other forms of cell division in that it increases the number of cells and nuclear mass without increasing the cytoplasmic mass. This means that with each successive subdivision, there is roughly half the cytoplasm in each daughter cell than before that division, and thus the ratio of nuclear to cytoplasmic material increases.[2]

Mechanism

The rapid cell cycles are facilitated by maintaining high levels of proteins that control cell cycle progression such as the cyclins and their associated cyclin-dependent kinases (CDKs). The complex cyclin B/CDK1 also known as MPF (maturation promoting factor) promotes entry into mitosis.

The processes of karyokinesis (mitosis) and cytokinesis work together to result in cleavage. The mitotic apparatus is made up of a central spindle and polar asters made up of polymers of tubulin protein called microtubules. The asters are nucleated by centrosomes and the centrosomes are organized by centrioles brought into the egg by the sperm as basal bodies. Cytokinesis is mediated by the contractile ring made up of polymers of actin protein called microfilaments. Karyokinesis and cytokinesis are independent but spatially and temporally coordinated processes. While mitosis can occur in the absence of cytokinesis, cytokinesis requires the mitotic apparatus.

The end of cleavage coincides with the beginning of zygotic transcription. This point in non-mammals is referred to as the midblastula transition and appears to be controlled by the nuclear-cytoplasmic ratio (about 1:6).

Types of cleavage

Determinate

Determinate cleavage (also called mosaic cleavage) is in most protostomes. It results in the developmental fate of the cells being set early in the embryo development. Each blastomere produced by early embryonic cleavage does not have the capacity to develop into a complete embryo.

Indeterminate

A cell can only be indeterminate (also called regulative) if it has a complete set of undisturbed animal/vegetal cytoarchitectural features. It is characteristic of deuterostomes—when the original cell in a deuterostome embryo divides, the two resulting cells can be separated, and each one can individually develop into a whole organism.

Holoblastic

In holoblastic cleavage, the zygote and blastomeres are completely divided during the cleavage, so the number of blastomeres doubles with each cleavage. In the absence of a large concentration of yolk, four major cleavage types can be observed in isolecithal cells (cells with a small, even distribution of yolk) or in mesolecithal cells or microlecithal cells (moderate concentration of yolk in a gradient)—bilateral holoblastic, radial holoblastic, rotational holoblastic, and spiral holoblastic, cleavage.[3] These holoblastic cleavage planes pass all the way through isolecithal zygotes during the process of cytokinesis. Coeloblastula is the next stage of development for eggs that undergo these radial cleavages. In holoblastic eggs, the first cleavage always occurs along the vegetal-animal axis of the egg, the second cleavage is perpendicular to the first. From here, the spatial arrangement of blastomeres can follow various patterns, due to different planes of cleavage, in various organisms.

Bilateral
The first cleavage results in bisection of the zygote into left and right halves. The following cleavage planes are centered on this axis and result in the two halves being mirror images of one another. In bilateral holoblastic cleavage, the divisions of the blastomeres are complete and separate; compared with bilateral meroblastic cleavage, in which the blastomeres stay partially connected.

Radial
Radial cleavage is characteristic of the deuterostomes, which include some vertebrates and echinoderms, in which the spindle axes are parallel or at right angles to the polar axis of the oocyte.

Rotational
Rotational cleavage involves a normal first division along the meridional axis, giving rise to two daughter cells. The way in which this cleavage differs is that one of the daughter cells divides meridionally, whilst the other divides equatorially.
Mammals display rotational cleavage, and an isolecithal distribution of yolk (sparsely and evenly distributed). Because the cells have only a small concentration of yolk, they require immediate implantation into the uterine wall in order to receive nutrients.
The nematode C. elegans, a popular developmental model organism, undergoes holoblastic rotational cell cleavage.[4]

Spiral
Spiral cleavage is conserved between many members of the lophotrochozoan taxa, referred to as Spiralia.[5] Most spiralians undergo equal spiral cleavage, although some undergo unequal cleavage (see below).[6] This group includes annelids, molluscs, and sipuncula. Spiral cleavage can vary between species, but generally the first two cell divisions result in four macromeres, also called blastomeres, (A, B, C, D) each representing one quadrant of the embryo. These first two cleavages are not oriented in planes that occur at right angles parallel to the animal-vegetal axis of the zygote.[5] At the 4-cell stage, the A and C macromeres meet at the animal pole, creating the animal cross-furrow, while the B and D macromeres meet at the vegetal pole, creating the vegetal cross-furrow.[7] With each successive cleavage cycle, the macromeres give rise to quartets of smaller micromeres at the animal pole.[8][9] The divisions that produce these quartets occur at an oblique angle, an angle that is not a multiple of 90 degrees, to the animal-vegetal axis.[9] Each quartet of micromeres is rotated relative to their parent macromere, and the chirality of this rotation differs between odd- and even-numbered quartets, meaning that there is alternating symmetry between the odd and even quartets.[5] In other words, the orientation of divisions that produces each quartet alternates between being clockwise and counterclockwise with respect to the animal pole.[9] The alternating cleavage pattern that occurs as the quartets are generated produces quartets of micromeres that reside in the cleavage furrows of the four macromeres.[7] When viewed from the animal pole, this arrangement of cells displays a spiral pattern.
D quadrant specification through equal and unequal cleavage mechanisms. At the 4-cell stage of equal cleavage, the D macromere has not been specified yet. It will be specified after the formation of the third quartet of micromeres. Unequal cleavage occurs in two ways: asymmetric positioning of the mitotic spindle, or through the formation of a polar lobe (PL).
Specification of the D macromere and is an important aspect of spiralian development. Although the primary axis, animal-vegetal, is determined during oogenesis, the secondary axis, dorsal-ventral, is determined by the specification of the D quadrant.[9] The D macromere facilitates cell divisions that differ from those produced by the other three macromeres. Cells of the D quadrant give rise to dorsal and posterior structures of the spiralian.[9] Two known mechanisms exist to specify the D quadrant. These mechanisms include equal cleavage and unequal cleavage.
In equal cleavage, the first two cell divisions produce four macromeres that are indistinguishable from one another. Each macromere has the potential of becoming the D macromere.[8] After the formation of the third quartet, one of the macromeres initiates maximum contact with the overlying micromeres in the animal pole of the embryo.[8][9] This contact is required to distinguish one macromere as the official D quadrant blastomere. In equally cleaving spiral embryos, the D quadrant is not specified until after the formation of the third quartet, when contact with the micromeres dictates one cell to become the future D blastomere. Once specified, the D blastomere signals to surrounding micromeres to lay out their cell fates.[9]
In unequal cleavage, the first two cell divisions are unequal producing four cells in which one cell is bigger than the other three. This larger cell is specified as the D macromere.[8][9] Unlike equally cleaving spiralians, the D macromere is specified at the four-cell stage during unequal cleavage. Unequal cleavage can occur in two ways. One method involves asymmetric positioning of the cleavage spindle.[9] This occurs when the aster at one pole attaches to the cell membrane, causing it to be much smaller than the aster at the other pole.[8] This results in an unequal cytokinesis, in which both macromeres inherit part of the animal region of the egg, but only the bigger macromere inherits the vegetal region.[8] The second mechanism of unequal cleavage involves the production of an enucleate, membrane bound, cytoplasmic protrusion, called a polar lobe.[8] This polar lobe forms at the vegetal pole during cleavage, and then gets shunted to the D blastomere.[7][8] The polar lobe contains vegetal cytoplasm, which becomes inherited by the future D macromere.[9]
Spiral cleavage in marine snail of the genus Trochus

Meroblastic

In the presence of a large concentration of yolk in the fertilized egg cell, the cell can undergo partial, or meroblastic, cleavage. Two major types of meroblastic cleavage are discoidal and superficial.[10]

  • Discoidal
In discoidal cleavage, the cleavage furrows do not penetrate the yolk. The embryo forms a disc of cells, called a blastodisc, on top of the yolk. Discoidal cleavage is commonly found in monotremes, birds, reptiles, and fish that have telolecithal egg cells (egg cells with the yolk concentrated at one end). The layer of cells that have incompletely divided and are in contact with the yolk are called the "syncytial layer".
  • Superficial
In superficial cleavage, mitosis occurs but not cytokinesis, resulting in a polynuclear cell. With the yolk positioned in the center of the egg cell, the nuclei migrate to the periphery of the egg, and the plasma membrane grows inward, partitioning the nuclei into individual cells. Superficial cleavage occurs in arthropods that have centrolecithal egg cells (egg cells with the yolk located in the center of the cell). This type of cleavage can work to promote synchronicity in developmental timing, such as in Drosophila.[11]
Summary of the main patterns of cleavage and yolk accumulation (after [12] and [13]).
I. Holoblastic (complete) cleavage II. Meroblastic (incomplete) cleavage

A. Isolecithal (sparse, evenly distributed yolk)

B. Mesolecithal (moderate vegetal yolk disposition)

A. Telolecithal (dense yolk throughout most of cell)

B. Centrolecithal (yolk in center of egg)

  • Superficial cleavage (most insects)

Mammals
"Morula" redirects here. For other uses, see Morula (disambiguation).
First stages of cleavage in a fertilized mammalian egg. Semidiagrammatic. z.p. Zona pellucida. p.gl. Polar bodies a. Two-cell stage b. Four-cell stage c. Eight-cell stage d, e. Morula stage

Mammals have a slow rate of division that is between 12 and 24 hours. These cellular divisions are asynchronous. Zygotic transcription starts at the two-, four-, or eight-cell stage. Cleavage is holoblastic and rotational.

In human embryonic development at the eight-cell stage, having undergone three cleavages the embryo goes through some changes as it develops into a blastocyst. At the eight-cell stage the blastomeres are round, and only loosely adhered. With further division in the process of compaction the cells become flattened, and develop an inside-out polarity that optimises the cell to cell contact between them. They begin to tightly adhere as gap junctions are formed, and tight junctions are developed with the other blastomeres.[14][15] At the 16–32 cell stage the compacted embryo is called a morula.[15][16] Once the embryo has divided into 16 cells, it begins to resemble a mulberry, hence the name morula (Latin, morus: mulberry).[17] With further compaction the individual outer blastomeres, the trophoblasts, become indistinguishable as they become organised into a thin sheet of tightly adhered epithelial cells. They are still enclosed within the zona pellucida. This compaction serves to make the structure watertight, to contain the fluid that the cells will later secrete.

In the human the morula enters the uterus after three or four days, and begins to take in fluid, as sodium-potassium pumps on the trophoblasts pump sodium into the morula, drawing in water from the maternal environment to become blastocoelic fluid. Hydrostatic pressure of the fluid creates a large cavity in the morula called a blastocoel. Embryoblast cells also known as the inner cell mass form a compact mass of cells at the embryonic pole on one side of the cavity that will go on to produce the embryo proper. The embryo is now termed a blastocyst.[15][18] The trophoblasts will eventually give rise to the embryonic contribution to the placenta called the chorion.

A single cell can be removed from a pre-compaction eight-cell embryo and used for genetic screening, and the embryo will recover.[19][20]

Differences exist between cleavage in placental mammals and other mammals.

References
  1. Gilbert, Scott F. (2000). "An Introduction to Early Developmental Processes". Developmental Biology (6th ed.). ISBN 978-0878932436.
  2. Forgács, G.; Newman, Stuart A. (2005). "Cleavage and blastula formation". Biological physics of the developing embryo. Cambridge University Press. p. 27. Bibcode:2005bpde.book.....F. ISBN 978-0-521-78337-8.
  3. Gilbert, Scott F. (2000). "Early Development of the Nematode Caenorhabditis elegans". Developmental Biology (6th ed.). ISBN 978-0878932436. Retrieved 2007-09-17.
  4. Gilbert, S. F. (2016). Developmental biology (11th ed.). Sinauer. p. 268. ISBN 9781605354705.
  5. Shankland, M.; Seaver, E. C. (2000). "Evolution of the bilaterian body plan: What have we learned from annelids?". Proceedings of the National Academy of Sciences. 97 (9): 4434–7. Bibcode:2000PNAS...97.4434S. doi:10.1073/pnas.97.9.4434. JSTOR 122407. PMC 34316. PMID 10781038.
  6. Henry, J. (2002). "Conserved Mechanism of Dorsoventral Axis Determination in Equal-Cleaving Spiralians". Developmental Biology. 248 (2): 343–355. doi:10.1006/dbio.2002.0741. PMID 12167409.
  7. Boyer, Barbara C.; Jonathan, Q. Henry (1998). "Evolutionary Modifications of the Spiralian Developmental Program". Integrative and Comparative Biology. 38 (4): 621–33. doi:10.1093/icb/38.4.621. JSTOR 4620189.
  8. Freeman, Gary; Lundelius, Judith W. (1992). "Evolutionary implications of the mode of D quadrant specification in coelomates with spiral cleavage". Journal of Evolutionary Biology. 5 (2): 205–47. doi:10.1046/j.1420-9101.1992.5020205.x. S2CID 85304565.
  9. Lambert, J. David; Nagy, Lisa M. (2003). "The MAPK cascade in equally cleaving spiralian embryos". Developmental Biology. 263 (2): 231–41. doi:10.1016/j.ydbio.2003.07.006. PMID 14597198.
  10. "Current Notes". Retrieved 2007-09-17.
  11. Gilbert SF. Developmental Biology 11th edition. Sunderland (MA): Sinauer Associates; 2014. Print
  12. Gilbert, S. F. (2003). Developmental biology (7th ed.). Sinauer. p. 214. ISBN 978-0-87893-258-0.
  13. Kardong, Kenneth V. (2006). Vertebrates: Comparative Anatomy, Function, Evolution (4th ed.). McGraw-Hill. pp. 158–64.
  14. Standring, Susan (2016). Gray's anatomy : the anatomical basis of clinical practice (Forty-first ed.). [Philadelphia]: Elsevier Limited. p. 165. ISBN 9780702052309.
  15. Schoenwolf, Gary C. (2015). Larsen's human embryology (Fifth ed.). Philadelphia, PA: Churchill Livingstone. pp. 35–36. ISBN 9781455706846.
  16. Gauster M, Moser G, Wernitznig S, Kupper N, Huppertz B (June 2022). "Early human trophoblast development: from morphology to function". Cellular and Molecular Life Sciences. 79 (6): 345. doi:10.1007/s00018-022-04377-0. PMC 9167809. PMID 35661923.
  17. Lawrence S., Sherman; et al., eds. (2001). Human embryology (3rd ed.). Elsevier Health Sciences. p. 20. ISBN 978-0-443-06583-5.
  18. Sadler TW (2010). Langman's medical embryology (11th ed.). Philadelphia: Lippincott William & Wilkins. p. 45. ISBN 9780781790697.
  19. Wilton, L (2005). "Preimplantation genetic diagnosis and chromosome analysis of blastomeres using comparative genomic hybridization". Human Reproduction Update. 11 (1): 33–41. doi:10.1093/humupd/dmh050. PMID 15569702.
  20. Kim HJ, Kim CH, Lee SM, Choe SA, Lee JY, Jee BC, Hwang D, Kim KC (September 2012). "Outcomes of preimplantation genetic diagnosis using either zona drilling with acidified Tyrode's solution or partial zona dissection". Clin Exp Reprod Med. 39 (3): 118–24. doi:10.5653/cerm.2012.39.3.118. PMC 3479235. PMID 23106043.

Bibliography

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