Expression of fibronectin and a fibronectin-binding molecule during preimplantation development in the mouse

Using an indirect immunofluorescent technique, expression ofcell surface fibronectin and a cell surface fibronectin-bindingmolecule was studied during mouse embryo preimplantation development.We also studied the expression of fibronectin on immunosurgicallyisolated inner cell masses (ICMs) and regenerated mouse blastocysts.Fibronectin and the fibronectin-binding molecule were not detectedat the morula stage. From the early to late blastocyst stage,fibronectin expression increased on the trophectoderm. Expressionof the fibronectin-binding molecule was found only in the polartrophectoderm region of the early blastocyst, then in the polarand mural trophectoderm regions of the middle blastocyst. Inthe late blastocyst stage, this fibronectin-binding moleculewas only present in the mural trophectoderm. Fibronectin expressionby ICMs of early blastocysts was more intense than that of lateblastocysts. After 24 h of culture, 10% of ICMs isolated fromearly blastocysts regenerated a trophectoderm which stainedintensively for fibronectin in the mural and polar trophectodermregions. After 48 h of culture, regenerated blastocyst-likestructures closely resembled the normally obtained late blastocystsand stained for fibronectin in the mural and polar trophectodermregions. The significance of the results is discussed in relationto mouse embryo development, trophectoderm formation and blastocystimplantation.     

Fertilization and Empryology: The effect of epidermal growth factor on growth and differentiation of mouse preimplantation embryos in vitro

The effect of epidermal growth factor (EGF) on embryonic growth,development, attachment and spreading in vitro was studied.EGF was added to 130 embryos at the 4-cell stage; to 128 embryosat the blastocyst stage; and to 147 embryos 24 h following spreading.Development of embryos from the 4-cell to the blastocyst stage,differentiation of the inner cell mass (ICM) and trophectoderm,and the occurrence of attachment and spreading were evaluated.Embryo development was significantly inhibited in cultures supplementedwith 100 ng/ml EGF compared to the controls (P < 0.001).Development of 4-cell embryos to blastocysts occurred in 25%of the EGF group compared to 85% of controls. Spreading occurredin 20% of 4-cell embryos and 30% of blastocysts treated withEGF, compared to 80 and 90% of corresponding controls. In embryosdeveloping from the 4-cell stage, massive growth of the ICMand inhibition of the trophectoderm occurred, whereas both ICMand trophectoderm were inhibited by EGF in embryos developingfrom the blastocyst stage. Following spreading, EGF caused massivegrowth of the ICM and regression of the trophectoderm. Our preliminaryresults show that EGF may be involved in the modulation andcontrol of early embryonic growth and differentiation.     

A retrospective analysis of the in-vitro development of 'spare' human in-vitro fertilization preimplantation embryos using 'in-house' prepared medium and 'Medi-Cult' commercial medium

In-house prepared medium was used routinely in our in-vitrofertilization (IVF) facility prior to the introduction of thecommercial ‘Medi-Cult’ products. A comparative studyof the in-vitro development of embryos cultured in two [T6 andEarle's balanced salt solution (EBSS)] humaninactivated serum(HlS)-supplemented media from days 0 to 5 showed that 44.7%(46/103) of the embryos developed to the blastocyst stage inthe T6 medium compared with 22.3% (23/103) in EBSS. Followingthe introduction of the commercial Medi-Cult IVF M2 medium,which is used routinely to culture fertilized eggs from days0 to 2, new baseline data were required for the in-vitro developmentof ‘spare’ embryos from days 2 to 5. When Medi-CultM3 medium was used, 35.6% (37/104) of the ‘spare’day 2 embryos achieved the blastocyst stage. However, if morphologicallysimilar (four normal nucleated blastomeres with no fragmentation)day 2 embryos were selected, an increase in the blastocyst rateto 50.0% (33/66) was achieved. This compared favourably withthe 45.0% blastocyst rate (published in the Medi-Cult literature)for M2/M3 medium cultured human embryos. A small series of experimentswith T6 $ HIS medium and human serum albumin (HSA)- supplementedHam's F-10, MCDB 302 and M3 media was undertaken to identifya suitable medium which could be used for the culture of M2medium day 2 embryos. Results show that M2 medium cultured embryosplaced in Ham's F-10 medium supplemented with 10 mg/ml HSA gavean acceptable 37.8% (14/45) blastocyst rate. Therefore, thismedium could be substituted for M3 medium in an emergency. Atotal of 483 IVF embryos donated by patients, which were surplusto the therapeutic IVF programme, were used for these studiesover a period of 30 months. Late day 2 IVF spare embryos wereassigned an embryo score based on a high-power phase-contrastmicroscopic examination prior to being placed in culture. Theembryo score provides an effective in-vitro parameter with whichembryos from different patients can be compared. The cleavageand development of individual embryos were monitored on days2 to 5. In some cases, the continuing normal development andviability of the day 5 cultured embryo were assessed by monitoringthe hatching, attachment and outgrowth of the cavitated blastocyst.     

Polyvinyl alcohol and amino acids as substitutes for bovine serum albumin in culture media for mouse preimplantation embryos

The effect of replacing bovine serum albumin (BSA) in a simpledefined medium (KSOM) with polyvinyl alcohol (PVA) and/or aminoacids on the percentages of mouse zygotes that develop to atleast the blastocyst stage and that hatch at least partiallyor completely is reported. Blastocysts could form when BSA wasreplaced with only PVA, but at a moderately reduced rate; however,partial hatching, and hence complete hatching, were severelyimpaired when BSA was replaced with only PVA. The substitutionof BSA with amino acids alone resulted in a high rate of blastocystformation and moderate impairment of hatching. The additionof PVA to BSA-free DSOM supplemented with amino acids had noextra effect. BSA had significant effects when added to BSA-freeKSOM supplemented with amino acids. The BSA caused a significantincrease in the rate of partial hatching, and may even havehad a small effect on the rate of blastocyst formation. Theresults also showed that glucose, at a high concentration of5.56 mM, does not inhibit the development of mouse zygotes tohatched blastocysts when cultured in KSOM supplemented withamino acids.     

Co-culture of 1-cell outbred mouse embryos on bovine kidney epithelial cells: effect on development, glycolytic activity, inner cell mass: trophectoderm ratios and viability

In an attempt to enhance embryo development, we have co-cultured1-cell OF1 mouse embryos on bovine kidney epithelial (Madine-Darbybovine kidney; MDBK) cells in a complex medium called complexmouse tubal fluid (cMTF; based on the energy substrate levelsfound in the mouse oviduct, containing non-essential amino acids,glutamine and EDTA). To determine the quality of the blastocystsobtained, we examined several parameters: morphology, totalcell numbers, inner cell mass (ICM): trophectoderm (TE) ratio,glycolytic activity and viability after transfer. A significantlylower number of blastocysts developed on MDBK cells comparedwith cMTF medium. cMTF blastocysts had a significantly higherglycolytic activity and a lower blastocyst cell number thanthose grown in co-culture, while both in-vitro groups had higherICM: TE ratios compared with in vivo. Blastocysts grown on MDBKcells displayed an elevated ICM number compared with those grownin cMTF medium alone. However, the percentage of fetuses aftertransfer remained drastically low in both culture groups comparedwith in-vivo blastocysts. In conclusion, co-culture did notincrease the number of zygotes reaching the blastocyst stage.Although co-culture blastocysts show some similarities to in-vivoembryos in cell number and glycolytic activity, no enhancementin viability was observed.     

One-step versus two-step culture of mouse preimplantation embryos: is there a difference?

BACKGROUND: A comparison has been made of the development of mouse zygotes in either one-step or two-step culture systems. METHODS: Embryo culture, blastocyst cell counts and embryo transfer were done. RESULTS: No significant differences were observed in the proportions of blastocysts, rates of hatching, numbers of cells in the inner cell mass (ICM) and trophectoderm (TE) that developed in protocols: one-step culture in potassium-enriched simplex optimized medium supplemented with glucose and amino acids (KSOMg(AA)), two-step culture in KSOMg(AA)/KSOMg(AA), and two-step culture in G1.2/G2.2. No gross abnormalities were observed in the fetuses that developed from zygotes in the one-step protocol using KSOMg(AA) and a two-step protocol using G1.2/G2.2. The body weights of these two groups of fetuses were not significantly different and no developmental abnormalities were observed. No significant differences were observed in the proportions of blastocysts, rates of hatching, numbers of cells in the ICM and TE that developed in protocols: one-step culture in KSOMg(AA), two-step culture in KSOMg(AA)/KSOMg(AA), and two-step culture in DM2/DM1. EDTA is not toxic to the initial cleavage stages of development at a concentration of 0.01 mmol/l in KSOMg(AA). CONCLUSIONS: Two-step culture protocols are sufficient for the support of preimplantation mouse development in vitro but they are not necessary.     

Cellular characterization of blastocysts derived from rabbit 4-, 8- and 16-cell embryos and isolated blastomeres cultured in vitro

The purpose of this study was to investigate the developmental potential of isolated rabbit blastomeres under various culture conditions to gain insight into their ability to form the two cell lineages of a viable blastocyst. Intact embryos at the 4-cell, 8-cell, 16-cell stages and blastomeres isolated from 4-, 8- and 16-cell rabbit embryos (1/4, 1/8 or 1/16 blastomeres respectively) were cultured in drops of one of three different media, each supplemented with either fetal calf serum (FCS), bovine serum albumin (BSA) or polyvinyl alcohol (PVA). The effects of the extracellular matrix fibronectin (FN) on the development of isolated rabbit blastomeres were also investigated. Supplementation of the medium with FCS yielded a higher (P < 0.05) proportion of blastocysts than BSA or PVA, predominantly from 1/4 blastomeres. No major differences were found between the three basic culture media. In 1/4, 1/8 or 1/16 blastomeres, blastocyst formation rates were greater (P < 0.05) in groups cultured in matrix-free (54.5, 59.6 and 54.6% respectively) than in FN-coated groups (35.4, 46.0 and 26.1% respectively). Only in blastocysts derived from 1/4 blastomeres, were the numbers of inner cell mass (ICM) and total cells of blastocysts higher (P < 0.05) in FN-coated groups than in matrix-free groups (12.7 +/- 1.1 versus 8.5 +/- 0.7 ICM, 73.8 +/- 3. 7 versus 57.8 +/- 3.3 total cells). The percentage of blastocysts derived from single blastomeres with ICM cells decreased with increasing cell stage of the parent embryos in FN-coated (93.6, 78.3 and 44.0%, respectively) as well as matrix-free groups (96.2, 69.3 and 55.2%). In FN-coated groups, after 96 h (1/4) or 72 h (1/8 and 1/16) of culture, approximately 20-30% of blastomeres did not develop into normal blastocysts but formed sheets with 30-50 cells attached to the bottom of the dishes. These results indicate that the development of rabbit blastomeres shares important characteristics with those from mouse and domestic species and may thus aid in developing an efficient culture system for blastomeres, derived from human embryos.     

Effects of SAPK/JNK inhibitors on preimplantation mouse embryo development are influenced greatly by the amount of stress induced by the media

Stress-activated protein kinase/c-Jun kinase (SAPK/JNK) is thought to be necessary for preimplantation embryonic development (Maekawa et al., 2005). However, media increases SAPK/JNK phosphorylation and these levels negatively correlate with embryonic development (Wang et al., 2005). Culture-induced stress could confuse analysis of the role of SAPK in development. In this study, we tested how SAPK/JNK inhibitors influence embryonic development in optimal and non-optimal media and define the contribution of cell survival and proliferation to the embryonic response to these media. SAPK/JNK inhibitors retard embryonic development in suboptimal Ham's F10, but improve development in optimal potassium (K+) simplex optimized media (KSOM) +AA. In KSOM + amino acids (KSOM+AA), two SAPK/JNK inhibitors increase the rate of cavitation and hatching. These data suggest that (i) SAPK/JNK mediates the response to culture stress, not normal preimplantation embryonic development and (ii) SAPK/JNK inhibitors may be useful in ameliorating embryo stress caused by culture. To define the effects of media, we assayed the contribution of cell survival and proliferation and the differences in total cell number of cultured embryos. Embryos cultured from E3.5+24 h in the suboptimal medium (Ham's F10) induced significant but small increases in TdT (terminal deoxynucleotidyl transferase)-mediated dUDP nick-end labelling (TUNEL) positive cells. Bromodeoxyuridine (BrdU) incorporation in suboptimal Ham's F10 was significantly lower than in optimal KSOM+AA, suggesting that cell cycle arrest also contributes to slower increase in cell number in stressful media. This is the first report where TUNEL and BrdU were both assayed to define the relative contribution of cell cycle/S phase commitment and apoptosis to lessened cell number increase during embryo culture.     

A prospective comparison of 'in house' and commercially prepared Earle's balanced salt solution in human in-vitro fertilization.

A prospective, randomized study was undertaken to compare the use of Earle's balanced salt solution (EBSS) prepared 'in house' with that produced commercially, in 448 cycles of therapeutic in-vitro fertilization. Outcome was assessed in terms of fertilization and cleavage rates, embryo morphology, and implantation rates following embryo transfer. The only differences that were found between the two media in any of the outcome parameters were in the number of cycles with failed fertilization (1/218 in 'in house' medium compared with 10/230 in commercially prepared medium; P = 0.0186), and in the rate at which embryos cleaved. Thus, while the median number of blastomeres per embryo was no different in the two groups at 46-49 h post insemination (three in embryos cultured in 'in-house' medium, compared with four in those cultured in commercially prepared medium; P > 0.1), the number of embryos per cycle that had cleaved to the 4-cell stage by 46-49 h post insemination was significantly greater in the Medi-Cult than in the EBSS medium (P < 0.001).     

Formulation of a protein-free medium for human assisted reproduction

The optimal concentrations of individual amino acids, antioxidants, vitamins, osmolytes and energy sources were determined using a 1-cell Swiss outbred (SO) and or F(1) [(CBAxC57BL/6J)xSO] mouse assay in Earle's balanced salt solution containing bovine serum albumin. Based on the findings of these experiments, a number of media were formulated. Of these, the medium showing optimal embryo development and a significantly higher blastocyst hatching rate was investigated further. A protein-free medium (ART-7) was formulated and assessed using 1-, 2- and 4-cell SO mouse embryos. The generation of viable human embryos in the ART-7 series of media in micro- and ultra micro-droplet culture under oil with and without cumulus co-culture following intracytoplasmic sperm injection (ICSI) was investigated. The quality of sibling day 2 human embryos generated in the ART-7 media series was statistically comparable to or better than control embryos. The ART-7 medium was not toxic to human spermatozoa. Fertilization by conventional IVF and subsequent embryo development was not affected. A clinical trial of ICSI-derived embryos generated in the protein-free medium, with and without cumulus co-culture, has resulted in clinical pregnancies (10 of 20 transfers) of which two have proceeded to term, and the remaining patients are in various stages of pregnancy.     

Non-invasive amino acid turnover predicts human embryo developmental capacity

BACKGROUND: IVF is limited by low success rates and a confounding high multiple birth rate contributing to prematurity, increased neonatal mortality and child handicap. These problems could be overcome if single embryos of known developmental competence could be selected for transfer on day 2/3 of development, but current methods, which rely on morphological appearance, are poor predictors of viability. METHODS: We have measured non-invasively the depletion/appearance (i.e. turnover) of a physiological mixture of 18 amino acids by single human embryos during in-vitro culture using high performance liquid chromatography. RESULTS: From the time of transfer (day 2/3), embryos with future competence to develop to the blastocyst stage (day 5/6) exhibit amino acid flux patterns distinct from those of embryos with similar morphological appearance which arrest. Significantly, the profiles of Ala, Arg, Gln, Met and Asn flux predict blastocyst potentiality at >95%. The amino acid most consistently depleted throughout development by those embryos which form blastocysts was leucine. Of the amino acids which were produced, the most striking was alanine, which appeared in increasing amounts throughout development. CONCLUSIONS: Non-invasive amino acid profiling has the potential to select developmentally competent single embryos for transfer, thereby increasing the success rate and eliminating multiple births in IVF.     

Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of beta-thalassaemia major

PGD is a well accepted reproductive choice for couples at genetic risk and involves the diagnosis and transfer of unaffected IVF embryos. PGD for monogenetic diseases is most commonly accomplished by the biopsy of one or two blastomeres from cleavage stage embryos, followed by PCR-based protocols. However, PCR-based DNA analysis of one or two cells is subject to several problems, including total PCR failure, or failure of one allele to amplify. Trophectoderm biopsy at the blastocyst stage enables the removal of more than two cells for diagnosis while being non-invasive to the inner cell mass which is destined for fetal development. The aim of this study was to develop a safe, reliable technique for the biopsy of trophectoderm cells from human blastocysts. This case report demonstrates that removal of trophectoderm cells prior to blastocyst transfer is compatible with implantation and development to term. Here we report successful PGD for beta-thalassaemia following trophectoderm cell biopsy from blastocysts and the birth of a healthy infant.     

Fertilization and early embryology: Alleviation of the '2-cell block' and development to the blastocyst of CF1 mouse embryos: role of amino acids, EDTA and physical parameters

The role of amino acids, ethylenediaminetetraacetic acid (EDTA),transferrin, oxygen, glucose, glutamine, taurine and ammoniumin CF1 mouse zygote development in culture was examined. Non-essentialamino acids and glutamine were shown to alleviate the 2-cellblock in culture, and acted in synergy with EDTA to facilitatedevelopment to the blastocyst stage. In the presence of aminoacids and EDTA, transferrin conferred no beneficial effect Developmentof zygotes was significantly impaired if amino acids were removedfrom the collection medium, even when they were subsequentlycultured in the presence of amino acids. Zygote developmentto the blastocyst stage was significantly improved when modularincubator chambers were used compared to using a conventionalincubator, and when an oxygen concentration of 7% was used asopposed to 20%. Addition of taurine to medium containing non-essentialamino acids had no effect on embryo development, whereas theremoval of glutamine and/or glucose from the culture mediumsignificantly reduced blastocyst cell number. Removal of glucosefrom the culture medium also resulted in a significant decreasein implantations. Ammonium, generated from the breakdown ofamino acids, significantly reduced blastocyst development EDTAwas found to confer its beneficial effects during the first48 h of culture, and indeed was inhibitory during the second48 h, resulting in loss of subsequent viability. In summary,the data demonstrate that development of CF1 zygotes to theblastocyst stage is readily achievable. In the presence of non-essentialamino acids and glutamine the removal of glucose is detrimentalto CF1 mouse embryo development in culture and reduces subsequentviability. Optimal development and maintenance of viabilityrequires more than one culture medium to support the preimplantationperiod.     

Possible involvement of crosstalk cell-adhesion mechanism by endometrial CD26/dipeptidyl peptidase IV and embryonal fibronectin in human blastocyst implantation

When human blastocysts hatch through the zona pellucida, gaining the ability to adhere to the endometrium, crosstalk between the embryo and the uterus may represent a successful outcome of their synchronized development and differentiation. CD26/dipeptidyl peptidase IV is known as a marker molecule of the implantation phase endometrium. To study the role of CD26 in implantation, 35 human hatched blastocysts were prepared by enzymatic treatment of expanded blastocysts that had been grown on schedule from frozen-thawed surplus embryos at the 2- or 4-cell stage. The blastocysts were placed on CD26-overexpressing or mock-transfected control monolayer cell cultures. The CD26-overexpression caused significantly higher blastocyst adhesion rate (53.3% versus 25.0%, P < 0.05) and significantly larger outgrowth area of trophectoderm (1.7-fold, P < 0.05). The second part of the present study was to show the expression of fibronectin, a CD26 ligand, in human preimplantation embryos, using the same donated resources. Fibronectin mRNA was detected by RT-PCR from the single hatched blastocyst (2/2) and from the single early blastocyst (3/6) but not from the single morula (0/5) samples. An indirect immunofluorescence technique verified the localization of fibronectin on the surface of the blastocyst. These results indicate that the adhesion mechanism by endometrial CD26 and embryonal fibronectin may be involved in human blastocyst implantation.     

Effects of taurine on human embryo development in vitro.

Glutamine and taurine are reported to be beneficial for mouse embryo development in vitro, and we have recently shown that glutamine improves human blastocyst formation in vitro. This randomized study compared the development of supernumerary human embryos in the presence of 1 mmol/l glutamine and/or 5 mmol/l taurine from the 2-4-cell stage to the blastocyst stage. Blastocyst development and cell numbers were similar in the presence of glutamine or taurine: 52.6% and 58.3% of the embryos reached the blastocyst stage, respectively. Pyruvate uptake was similar in the presence of glutamine or taurine throughout development, as was lactate production after the 8-cell stage. Before this stage, lactate production was 4-fold higher in the presence of taurine (P < 0.001). The proportion of embryos reaching the blastocyst stage was similar with glutamine alone or with glutamine and taurine (62.5% and 47.2% respectively), as were the blastocyst cell numbers (63.0 +/- 4.6 and 61.0 +/- 5.1 respectively). In conclusion, taurine supports development of 2-4-cell human embryos to the blastocyst stage, although it does not further augment the beneficial effects of glutamine.     

Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage

Normally fertilized human embryos biopsied 3 days after in-vitro fertilization (IVF) have been examined for effects on viability and development in vitro after removal of one or two cells at the 8-cell stage (1/8 and 2/8) from each embryo. A high proportion of 7/8 and 6/8 biopsied and unmanipulated embryos developed to the blastocyst stage between days 5 and 6 (79, 71 and 59%, respectively), and many biopsied embryos (56%) hatched from the zona pellucida in vitro. The viability of biopsied embryos which developed to the blastocyst stage was assessed by daily non-invasive measurement of the uptake of two energy substrates, glucose and pyruvate. Uptake of both substrates was generally lower in 7/8 and 6/8 biopsied embryos but only in proportion to the reduced cellular mass. The total cell number and the numbers of both trophectoderm (TE) and inner cell mass (ICM) cells in biopsied embryos at the blastocyst stage, counted by differential labelling of their nuclei, were also reduced in proportion but the ratio of ICM to TE cells was maintained in both 7/8 and 6/8 biopsied embryos. We conclude that removal of one or two cells at the 8-cell stage, while reducing the cellular mass, does not adversely affect the preimplantation/development of biopsied embryos in vitro and suggest that this approach could be used for preimplantation diagnosis of genetic defects.     

Enhanced recruitment of motile spermatozoa by prostasome inclusion in swim-up medium

Prostasomes, which are prostate-derived organelles, were purifiedfrom human seminal plasma for inclusion in Earle's balancedsalt solution(EBSS) medium with or without human serum albumin.These media were used for swim-up experiments and the the subsequentanalyses of sperm motility parameters at different incubtiontimes. The yield of motile spermatozoa after swim-up in EBSSmedium enriched with boiled prostasomes was increased by 32%compared with EBSS containing albumin. Native prostasomes wereless active. Combinations of albumin and either prostasomesor boiled prostasomes significantly increased the recovery ofmotile spermatozoa and also increased the revocery of motilespermatozoa and also increased the percentage of spermatozoaand also increased the percentage of spermatozoa displayingprogressive motility after 1 h of incubation. Media lackingalbumin showed lower values regarding progressive motility after22 h of incubation. A beneficial effect of prostasomes was notedon lateral head displacement and percentage of hyperactive spermatozoaduring the first 6 h of incubation. These results suggest thatinclusion of prostasomes, especially boiled prostasomes, inswim-up media may improve the recovery of hyperactive motilespermatozoa forup to 6 h in cases of established male factorinfertility, and consequently increase the oportunities forfertilization.     

Fertilization and early embryolgoy: Lineage tracing demonstrates that blastomeres of early cleavage-stage human pre-embryos contribute to both trophectoderm and inner cell mass

We injected a fluorescent lineage tracer (Texas Red-lysinedextran)into individual blastomeres of donated human diploid 2- to 8-cellpre-embryos and cultured them to blastocysts. Once pre-embryosreached the expanded blastocyst stage, they were fixed and examinedin a scanning confocal microscope to identify the location offluorescent tracer. In successfully injected pre-embryos thatdeveloped to expanded blastocysts, we found that randomly injectedblastomeres formed both trophectoderm (TE) and inner cell mass(ICM). More labelled progeny were found in TE than in ICM. Ourresults show that individual early blastomeres are not yet committedto form either TE or ICM but instead can form both rudiments.     

An investigation of the fate of cells transplanted orthotopically between morulae/nascent blastocysts in the mouse

A technique has been devised for selectively replacing someinside cells (ICs) or outside cells (OCs) of late morulae/nascentblastocysts with corresponding cells from genetically dissimilar,synchronous embryos. The main purpose was to determine whetherthe inner cell mass (ICM) contributes cells to the overlyingpolar trophectoderm at any stage during the blastocyst phaseof development. Notwithstanding the high incidence and levelof chimaerism in ICM derivatives of postimplantation conceptusesobtained in the IC transplantation experiments, trophoblasttissue was composed entirely of host cells in the majority ofcases. Even where a donor IC contribution to trophoblast wasdetected there were strong grounds for suspecting that it wasdue to tissue contamination rather than genuine chimaerism.Thus, not only did such contributions differ in both level anddistribution from those produced by transplantation of OCs butthey also varied markedly in frequency according to the dayof gestation on which conceptuses were dissected. The possibilitythat ICs regularly colonize the polar trophectoderm but failto persist there was excluded by the results of short-term transplantation experiments using an in-situ genetic marker. These findingsoffer no support for the hypothesis that the ICM serves as apopulation of stem cells for the trophectoderm as well as theprimitive endoderm and ectoderm during normal development. Thefrequency of chimaerism was lower in OC than IC transplantationexperiments. Nevertheless, in a substantial proportion of chimaeras,OCs colonized derivatives of the ICM. This is consistent withevidence from other studies that some outside cells divide differentiallyat 5th cleavage to produce an OC plus an IC rather than twoOCs.     

Granulocyte-macrophage colony-stimulating factor promotes human blastocyst development in vitro

The cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) is synthesized in the female reproductive tract and has been implicated in the growth and development of the preimplantation embryo in rodent and livestock species. To examine the effect of GM-CSF on human embryo development in vitro, surplus frozen 2-4-cell embryos were cultured in media supplemented with 2 ng/ml recombinant human GM-CSF. The addition of cytokine increased the proportion of embryos that developed to the blastocyst stage from 30 to 76%. The developmental competence of these blastocysts, as assessed by hatching and attachment to extracellular matrix-coated culture dishes, was also improved by GM-CSF. The period in culture required for 50% of the total number of blastocysts to form was reduced by 14 h, and blastocysts grown in GM-CSF were found to contain approximately 35% more cells, due primarily to an increase in the size of the inner cell mass. The beneficial effect of GM-CSF was exerted in each of two sequential media systems (IVF-50/S2 and G1. 2/G2.2) and was independent of the formulation of recombinant cytokine that was used. These data indicate that GM-CSF may have a physiological role in promoting the development of the human embryo as it traverses the reproductive tract in vivo, and suggest that addition of this cytokine to embryo culture media may improve the yield of implantation-competent blastocysts in human in-vitro fertilization programmes.