Determinative mechanisms in secondary muscle lineages of ascidian embryos: development of muscle-specific features in isolated muscle progenitor cells

Development ◽  
1990 ◽  
Vol 108 (4) ◽  
pp. 559-568 ◽  
Author(s):  
H. Nishida

Muscle cells of the ascidian larva originate from three different lines of progenitor cells, the B-line, A-line and b-line. Experiments with 8-cell embryos have indicated that isolated blastomeres of the B-line (primary) muscle lineage show autonomous development of a muscle-specific enzyme, whereas blastomeres of the A-line and b-line (secondary) muscle lineage rarely develop the enzyme in isolation. In order to study the mechanisms by which different lines of progenitors are determined to give rise to muscle, blastomeres were isolated from embryos of Halocynthia roretzi at the later cleavage stages when conspicuous restriction of the developmental fate of blastomeres had already occurred. Partial embryos derived from B-line muscle-lineage cells of the 64-cell embryo (B7.4, B7.5 and B7.8) showed autonomous expression of specific features of muscle cells (acetylcholinesterase, filamentous actin and muscle-specific antigen). In contrast, b-line muscle-lineage cells, even those isolated from the 110-cell embryo (b8.17 and b8.19), did not express any muscle-specific features, even though their developmental fate was mainly restricted to generation of muscle. Isolated A-line cells from the 64-cell embryos (A7.8) did not show any features of muscle differentiation, whereas some isolated A-line cells from the 110-cell embryos (A8.16) developed all three above-mentioned features of muscle cells. This transition was shown to occur during the eighth cell cycle. These results suggest that the mechanism involved in the process of determination of the secondary-lineage muscle cells differs from that of the primary-lineage muscle cells. Interaction with cells of other lineages may be required for the determination of secondary precursors to muscle cells. The presumptive b-line and A-line muscle cells that failed to express muscle-specific features in isolation did not develop into epidermal cells. Thus, although interactions between cells may be required for muscle determination in secondary lineages, the process may represent a permissive type of induction and may differ from the processes of induction of mesoderm in amphibian embryos.

1991 ◽  
Vol 69 (11) ◽  
pp. 2811-2818 ◽  
Author(s):  
William R. Bates

The determination of cell fates in ascidian embryos is thought to be mediated primarily by factors localized in the cytoplasm. Morphogenetic factors were studied in ascidian eggs and early cleavage stage embryos by the partial deletion of blastomeres and by microinjection of sperm cells into anucleate, myoplasm-deficient egg fragments. In the first series of experiments, regions of blastomeres comprised of 20–30% of the volume of one blastomere were deleted from two- and four-celled embryos. Most of the embryos exhibited regulative capabilities, in that normal tadpole larvae developed from the operated embryos, irrespective of the deletion site. In a second series of experiments, the expression of endodermal alkaline phosphatase (AP) and muscle acetylcholinesterase (AchE) were tested in myoplasm-deficient egg fragments that were injected with sperm cells. After the unoperated controls had developed into tadpoles, myoplasm-deficient fragments injected with sperm cells were scored for their ability to express AP and AchE activity. Many of the myoplasm-deficient fragments that contained injected sperm cells expressed AP activity, whereas uninjected myoplasm-deficient fragments did not exhibit AP activity. When myoplasm-deficient fragments injected with sperm cells were tested for their ability to express AchE activity, none of the fragments expressed this muscle cell marker. Similar results were obtained using two species, Halocynthia roretzi and Styelaplicata. These results suggest that nuclear events are required for the expression of AP and that the myoplasmic region of the fertilized egg contains muscle cell determinants.


2010 ◽  
Vol 30 (10) ◽  
pp. 1890-1896 ◽  
Author(s):  
Jan-Marcus Daniel ◽  
Wiebke Bielenberg ◽  
Philipp Stieger ◽  
Soenke Weinert ◽  
Harald Tillmanns ◽  
...  

Development ◽  
1980 ◽  
Vol 55 (1) ◽  
pp. 343-354
Author(s):  
J. R. Whittaker

This research shows that myoplasmic crescent material of the ascidian egg has both functional autonomy and functional specificity in establishing the differentiation pathway of muscle lineage cells. The cytoplasmic segregation pattern in eggs of Styela plicata was altered by compression of the embryos during third cleavage. This caused a meridional division instead of the normal equatorial third cleavage; first and second cleavages are meridional. Since eggs of S. plicata have a pronounced yellow myoplasmic crescent, one observes directly that third cleavage under compression resulted in a flat 8-cell stage with four cells containing yellow myoplasm instead of the two myoplasm-containing cells that would be formed by normal equatorial division at third cleavage. If such altered 8-cell-stage embryos were released from compression and kept from undergoing further divisions by continuous treatment with cytochalasin B, some embryos eventually developed histospecific acetylcholinesterase in three and four cells instead of in just the two muscle lineage cells found in cleavage-arrested normal 8-cell stages. The wider myoplasmic distribution effected by altering the division plane at third cleavage apparently caused a change in developmental fate of the extra cells receiving myoplasm. This meridional third cleavage also resulted in a changed nuclear lineage pattern. Two nuclei that would ordinarily be in ectodermal lineage cells after third cleavage were now associated with yellow myoplasm. Acetylcholinesterase development in these cells demonstrates that nuclear lineages are not responsible for muscle acetylcholinesterase development in the ascidian embryo.


Development ◽  
1994 ◽  
Vol 120 (2) ◽  
pp. 235-243 ◽  
Author(s):  
H. Nishida

Embryogenesis in ascidians is of the mosaic type. This property suggests the presence of cytoplasmic factors in the egg that are responsible for specification of the developmental fates of early blastomeres. The epidermal cells that surround the entire tadpole larva originate exclusively from blastomeres of the animal hemisphere of early embryos. To obtain direct evidence for cytoplasmic determinants of epidermis fate, we carried out cytoplasmic transfer experiments by fusing blastomeres and anucleate cell fragments from various regions of eggs and embryos. Initially, presumptive non-epidermis blastomeres (blastomeres from the vegetal hemisphere) were fused to cytoplasmic fragments from various regions of blastomeres of 8-cell embryos of Halocynthia roretzi, and development of epidermal cells was monitored by following the expression of an epidermis- specific antigen, as well as by observations of morphology and the secretion of larval tunic materials. Formation of epidermis was observed when vegetal blastomeres were fused with cytoplasmic fragments from the presumptive epidermis blastomeres. The results suggested that cytoplasmic factors that promoted epidermis differentiation (epidermis determinants) were present in epidermis progenitors. Vegetal blastomeres only manifested this change in fate when fused with cytoplasmic fragments of roughly equal or larger size. Next, to examine the presence and localization of epidermis determinants in the uncleaved egg, cytoplasmic fragments from various regions of unfertilized and fertilized eggs were fused with the vegetal blastomeres. The results suggested that epidermis determinants were already present in unfertilized eggs and that they were segregated by movements of the ooplasm after fertilization. After the first phase of ooplasmic segregation, these determinants were widely distributed, with the highest activity being located in the equatorial region. There were no indications of regional differences in the activity within the equatorial region of eggs at this stage. After the second phase of ooplasmic segregation, prior to the first cleavage, the activity moved in the animal direction, namely, to the animal hemisphere, from which future epidermis-lineage blastomeres are normally formed.


2006 ◽  
Vol 26 (12) ◽  
pp. 2696-2702 ◽  
Author(s):  
Jacob F. Bentzon ◽  
Charlotte Weile ◽  
Claus S. Sondergaard ◽  
Johnny Hindkjaer ◽  
Moustapha Kassem ◽  
...  

2020 ◽  
Vol 17 (34) ◽  
pp. 93-111
Author(s):  
Saule Amangeldievna MUSSABEKOVA

Identifying semen stains on clothing and bedding is a crucial component in investigating cases of sexual assault. In some cases, clothing and bedding have already been washed before they were removed and sent for forensic examination. There is insufficient data on best practices for handling traces of semen on clothes after washing. This work aimed to study the possibility of identifying traces of semen on clothes after washing using widely used techniques. To simulate typical physical evidence, donor semen samples were applied to pieces of clothing made from various fabrics. The clothes were washed under multiple conditions (with the help of nonbiological and biological (enzyme-containing) agents, and across numerous washing machines). After washing, the washing stains were characterized by the presence of fluorescence signal, spermatozoa (Koren – Stokis method), the determination of acid phosphatase, prostate-specific antigen and semenogelin, as well as the results of serological research according to the AB0 system and DNA analysis. Clothing analysis using these methods was shown to be effective in experimental conditions. However, the presence of enzymes as detergent components designed to destroy biogenic stains significantly affect the results of the identification of semen stains. It has been established that the full genetic profile can be obtained from semen stains even after washing three times. Different strategies are needed to detect, select and identify semen stains depending on the circumstances of a case. It is recommended to examine clothing and bedding, even if the specimens were previously washed.


Life Sciences ◽  
2009 ◽  
Vol 84 (13-14) ◽  
pp. 394-401 ◽  
Author(s):  
Mei Han ◽  
Li-Hua Dong ◽  
Bin Zheng ◽  
Jian-Hong Shi ◽  
Jin-Kun Wen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document