ABSTRACT
Lung mesenchyme is able to support budding and cytodifferentiation of salivary epithelial rudiments in vitro. No difference in response was found between submandibular and parotid epithelium from mouse or rat.
There are several further features of this result, which is contradictory to previous findings. (1) Lung mesenchyme is quantitatively less effective than submandibular mesenchyme for supporting submandibular morphogenesis. At least part of this difference is attributed to the inability of submandibular epithelium to replace lung epithelium in supporting the growth of lung mesenchyme. (2) Rat lung mesenchyme is quantitatively more effective than mouse lung mesenchyme when recombined with mouse submandibular epithelium. This may be at least partly due to mouse lung being more easily damaged by the procedures used. (3) Whereas the response of submandibular epithelium to submandibular mesenchyme is equally good on an agar or Millipore filter (MF) substratum, the response to lung mesenchyme is severely reduced or eliminated on MF. This difference is interpreted in terms of different mesenchymal cell densities necessary for submandibular or lung mesenchyme to support branching morphogenesis.
Salivary buds formed in lung mesenchyme after 6 days are smaller and more closely packed than in salivary mesenchyme. In these heterotypic recombinates, the accumulation of amylase-resistant, PAS-positive material in the buds is initially accelerated and the tubular epithelium accumulates glycogen.
INTRODUCTION
The ability of mouse submandibular gland epithelium to undergo branching morphogenesis in vitro has been so far held to depend on a specific requirement for salivary mesenchyme: morphogenesis has been found to occur only in the presence of mouse submandibular (Grobstein, 1953) and parotid (Grobstein, 1967), or chick submandibular (Sherman, 1960) mesenchyme, but not in lung (Grobstein, 1953; Spooner & Wessells, 1972), mammary (Kratochwil, 1969), metanephric, mandibular arch, or limb-bud mesenchyme (Grobstein, 1953). In contrast, mouse submandibular mesenchyme is able to support the development of non-salivary epithelia, such as that of the thymus (Auerbach, 1960), pancreas (Golosow & Grobstein, 1962; Fell & Grobstein, 1968) and mammary gland (Kratochwil, 1969). Such results led to the proposal that salivary mesenchyme possesses both a mesenchyme common factor or property, shared with other mesenchymes, and a mesenchyme specific factor or property unique to salivary mesenchyme and essential for salivary morphogenesis (Grobstein, 1967).
In apparent contrast to mouse submandibular, rat parotid epithelium was shown to be able to undergo morphogenesis and functional differentiation in rat lung mesenchyme (Lawson, 1972). Also, Cunha (1972) has shown that mouse submandibular epithelium develops extensively in mesenchyme from male secondary sex organs when the recombinates are cultured in the anterior chamber of the eye.
These results made desirable a reinvestigation of mesenchyme requirement in salivary development. Attention has been concentrated on recombinates of salivary epithelium with lung mesenchyme in vitro : the relative importance of differences within the salivary system, species differences, mesenchyme mass, and culture conditions has been assessed.
MATERIALS AND METHODS
Animals
Wistar rats and Swiss mice were used. In calculating the embryonic age, the morning on which vaginal sperm (rats) or a copulation plug (mice) were found after overnight mating was counted as day 1.
Tissues
Parotid glands from 17-day-old foetuses of rats and 15-day-old foetuses of mice, submandibular glands from 16-day-old foetuses of rats and 14-day-old foetuses of mice, and lungs from 13-and 14-day-old foetuses of rats and 12-and 13-day-old foetuses of mice were used. The morphogenetic stages of these organs are shown in Fig. 1.
Tissue culture
As described previously (Lawson, 1972), the rudiments were separated into epithelial and mesenchymal components by trypsin-pancreatin treatment and dissection, recombined on an agar film which was supported by a frame of cellulose acetate net, and cultured on a medium of cock plasma and chick embryo extract in a humidified atmosphere of air and 5 % CO2. Cultures that were maintained for 12 days were transferred to 45 % N2, 50 % O2 and 5 % CO2 on the 9th day. Unless mentioned otherwise the epithelium from one salivary rudiment was recombined with mesenchyme from two salivary glands or lungs. In experiments in which recombinates were made directly on the platform of a Millipore filter (MF) assembly (modified from Grobstein, 1956) the nutrient medium (referred to as liquid medium) was Ham’s F 12 with 100 i.u. penicillin and streptomycin/ml, 10 % foetal bovine serum, and 10 % chick embryo extract.
Histology
Tissues were fixed in Helly’s or Carnoy’s fluid and sections were stained with PAS (periodic acid-Schiff), alcian blue at pH 2·8, and Mayer’s haemalum. Glycogen was detected by comparing amylase-treated sections with adjacent Control sections. The sections were incubated for 30 min at 37 °C in 3 i.u. amylase (Worthington, 3×crystallized)/ml 0·02 M phosphate buffer with 0·007M sodium chloride at pH 6·8.
In one series of experiments the critical electrolyte concentration-alcian blue method for acidic glycosaminoglycans (Scott & Dorling, 1965) was used.
Criteria for salivary development
(1) Morphogenesis
A quantitative estimate of epithelial morphogenesis was obtained by counting the number of buds in camera lucida tracings of the explants drawn under standardized conditions of lighting and magnification. Buds were defined on the basis of indentation of the epithelial outline into the epithelium, rather than extension of the epithelium into the mesenchyme: the two sides of the indentation were required to have an angle of less than 135° on the mesenchymal side; each side would then belong to a different bud. This method underestimates newly initiated buds that have no lateral extension in the plane of the drawing; well-formed vertical clefts are easily visible and were assumed to have an angle of less than 135°. The method is unreliable after 5–6 days of culture when fast-growing recombinates have thickened and buds overlap.
In one experiment the volumes of epithelium and mesenchyme in the re-combinates after 6 days culture were measured from sections using a point grid method. The number of mesenchyme cells per unit volume was measured by counting mesenchyme nuclei in 12 standard areas of mesenchyme (2328 μm2) per sectioned explant.
(2) Cytodifferentiation
The presence of amylase-resistant, PAS-positive material was scored since such material accumulates in the terminal buds towards the end of the foetal period in the submandibular (Gerstner, Flon & Butcher, 1963; Szymanska, 1963; Di Giovine Vecchione, 1967) and perinatally in the parotid (Bignardi, 1961; Shubnikova & Chunaeva, 1966; Lawson, 1970; Redman & Sreebny, 1971) and also in both glands in vitro(Di Giovine Vecchione, 1967; Lawson, 1970, 1972). No such accumulation has been found in the epithelium in vitro in the absence of morphogenesis.
Mesenchymal protein
The initial protein content of representative samples of mesenchyme was determined by the Folin-Lowry procedure (Lowry, Rosebrough, Farr & Randall, 1951).
Statistical analysis
The distribution of attributes of morphogenesis and of cytodifferentiation were tested with the χ2 test.
The effects of different treatments on the number of epithelial buds present at any one time, on the final volumes of epithelium and mesenchyme, and on the number of mesenchyme cells per explant were tested by analysis of variance after transformation of the data to the logarithmic scale. This transformation was justified since the variances of the means after different treatments differed significantly before, but not after, transformation. The transformation was not required for analysing the data on cells per unit volume, which appeared to be normally distributed with similar variances. A randomized block design was used for all experiments in which analysis of variance was applied.
RESULTS
Development of salivary epithelium in lung mesenchyme
Parotid and submandibular epithelia from both mouse and rat were recom-bined with their own mesenchyme and with homospecific lung mesenchyme (14-day-old foetuses of rat, 12-and 13-day-old foetuses of mouse).
Morphogenesis occurred in all types of recombinate (Table 1) and there was no significant difference in the proportion showing morphogenesis between homotypic and heterotypic recombinates in either species, or between parotid and submandibular epithelium. However, mouse salivary/lung recombinates did not increase in overall size after 2 – 3 days, but began to lose cells and finally became very small. After continued culture, cytodifferentiation was found in all types of recombinate. Rat salivary epithelium differentiated as well in lung as in its own mesenchyme (Table 1 ; Fig. 2A, B); mouse salivary epithelium differ-entiated in mouse lung mesenchyme (Table 1; Fig. 2C, D), but there was a significant number of negative results(, degrees of freedom = 1, P < 0 · 01), presumably due to the progressive loss of mesenchyme cells.
Heterotypic, heterospecific recombinates of mouse salivary epithelium with rat lung mesenchyme were also made. These did not lose cells from the edge of the explant or diminish in size after three days: their morphogenesis and cyto-differentiation were comparable to the heterotypic, homospecific rat recombi-nates (Table 1 ; Fig. 2E). This suggests a difference in behaviour between rat and mouse lung mesenchyme, rather than a difference between rat and mouse salivary epithelia in their ability to respond to lung mesenchyme.
Since both parotid and submandibular epithelium from both rat and mouse are able to develop in lung mesenchyme it is concluded that there is no mesen-chyme-specific factor unique to salivary mesenchyme and essential for salivary epithelial morphogenesis.
Effect of mesenchyme mass on submandibular morphogenesis
(a) Mouse recombinates
The possibility that the initial mass of mesenchyme in the recombinate is a critical factor for supporting morphogenesis was tested by combining the epithelium from one mouse submandibular rudiment with the mesenchyme from one, two, three or four submandibulars, 12-day lungs, or 13-day lungs. ‘One’ lung mesenchyme was defined as half the mesenchyme obtained from a pair of lungs (the right lung is about twice the size of the left lung at the stages used). The protein content of mesenchyme from all three sources was measured in other prospective litters (Table 2), showing that the mesenchyme from ‘one’13-day lung had approximately twice the amount of protein as ‘one’ 12-day lung or 14-day submandibular. The high variation in the values for lung mesen-chyme appears to be due to the very rapid growth of this organ, since the aver-age protein content of the mesenchyme is correlated with the average number of epithelial buds per pair of lungs (Fig. 3).
The experiment was set up as a 4 × 3 factorial in three replicates, with dupli-cates within each replicate; N(total number of expiants) = 72.
After the initial rounding-up, the epithelium expanded considerably in lung mesenchyme forming large, flat buds which were then further subdivided by clefts (Fig. 4C, D). In inadequate amounts of mesenchyme this expansion was restricted and subsequent morphogenesis was negligible (Fig. 4B). The diminish-ing overall size of the heterotypic recombinates after the second day of culture, compared with the continued growth of the homotypic recombinates, is also evident in Fig. 4. A cyst appeared in the epithelium between the second and third day and by the sixth day had expanded, excluding the buds to the periphery.
Varying the initial mass of submandibular mesenchyme had no effect on the rate of bud formation (Fig. 5 A). However ‘two’, ‘three’ and ‘four’ 13-day lung mesenchymes supported substantial bud formation, ‘one’ significantly less (Fig. 5C). ‘Three’ and ‘four’ 12-day lung mesenchymes supported substantial epithelial morphogenesis, ‘two’ significantly less, whereas ‘one’ 12-day lung mesenchyme failed to support significant morphogenesis (Fig. 5B), although the initial amount of mesenchyme present, estimated as protein, was about the same as one submandibular mesenchyme.
Thus relatively more mouse lung mesenchyme than submandibular mesen-chyme is needed to support morphogenesis of submandibular epithelium.
(b) Mouse recombinates on MF and liquid medium
If the previously reported failure of mouse lung mesenchyme to support submandibular epithelial morphogenesis (Grobstein, 1953; Spooner & Wessells, 1972) was due solely to insufficient mesenchyme, the presence of large quantities of lung mesenchyme should ensure morphogenesis under the same culture conditions. Culture conditions similar to those used by Spooner & Wessells (MF over liquid medium) were chosen since these are currently in general use for organ cultures. Mouse submandibular epithelium was recombined with ‘two’, ‘four’ or ‘six’ 12-day lung mesenchymes. Homotypic control recombi-nates of submandibular epithelium with two submandibular mesenchymes and of left lung epithelium with ‘two’ lung mesenchymes were also made.
Increasing initial amounts of lungmesenchyme supported some morphogenesis of submandibular epithelium (Fig. 6), but much less than was expected. When epithelial morphology was classified into three groups (–, no buds (Fig. 6A); +, buds but no branching (Fig. 6B); +, branched buds (Fig. 6C)) it was found that morphogenesis was better in ‘four’ and ‘six’ lung mesenchymes than in ‘two’ (Table 3; χ2 for heterotypic recombinates, 2 vs. 4 = 14 · 92, 2 vs. 6 = 14 · 24, P < 0 · 001, degrees of freedom = 2).
Thus a relatively large quantity of mouse lung mesenchyme is necessary for submandibular epithelium to achieve a very limited morphogenesis when the recombinates are supported by MF over liquid medium.
(c) Mouse submandibular epithelium in rat lung mesenchyme
Unlike the recombinates of mouse salivary epithelium in mouse lung mesen-chyme, which became smaller after 2 or 3 days on agar and plasma-embryo extract, recombinates of rat or mouse salivary epithelia in rat lung mesenchyme maintained their size and did not lose mesenchyme cells (p. 473), suggesting that mouse and rat lung mesenchymes differ in their interaction with salivary epithelium.
To test whether 14-day rat lung mesenchyme is quantitatively equivalent to mouse submandibular mesenchyme for mouse submandibular epithelial de-velopment, a half, one and two masses of each were recombined with mouse submandibular epithelium in a 3 × 2 factorial experiment in three replicates, with triplicates within each replicate; N = 54. In addition, a half, one and two masses of lung mesenchyme were recombined with the epithelium of the left lung. Equivalent masses of mesenchyme were taken on the basis of the expected protein content (Table 2) and subsequently checked on random samples from the same litters as used in the experiment. The estimated initial protein content per unit mass of mesenchyme (based on that from one sub-mandibular) for the three replicates was: submandibular – 2· 90 μg, 3· 99 μg, 2· 65 μg, mean 3· 18 μg; lung –2· 46 μg, 3· 23 μg, 3· 05 μg, mean 2· 91 μg. The effect of initial mesenchymal mass on bud number (Fig. 7; P < 0· 001 at 2, 3, 4 and 6 days) and on final epithelial volume (Fig. 8;P < 0· 001) may be misleading, since the smaller masses of mesenchyme were not able to enclose the epithelium com-pletely. The number of salivary buds was 37 % higher in submandibular than in lung mesenchyme at 2 days (P < 0· 05), 30 % higher at 3 and 4 days (P < 0· 1) and 55 % higher at 6 days (P = 0· 01).
The final difference between homo-and heterotypic recombinates was even more pronounced when the volumes of epithelium after 6 days culture were compared (Fig. 8): the volume of salivary epithelium present in lung mesen-chyme was only 30–50% of that in submandibular mesenchyme (P < 0·001). The final volume of lung mesenchyme in the heterotypic recombinates also was only 30–50 % of the submandibular mesenchyme in the homotypic recombinates (P < 0·001) and 19–26% of mesenchyme in the homotypic lung recombinates (P < 0·001). Taking into account the data showing that lung mesenchyme cells are more densely packed, in both homo-and heterotypic recombinates, than submandibular mesenchymal cells (Table 4), calculation showed that the heterotypic recombinates contained half as many mesenchyme cells as the homotypic submandibular recombinates, which again had half as many mesenchyme cells as the homotypic lung recombinates (Table 4, P < 0-001 for all comparisons).
It is concluded that small amounts of rat lung mesenchyme (equivalent in mass to half a mouse submandibular mesenchyme) can support submandibular budding. However, the reinitiation of budding by submandibular epithelium after trypsinization is slower in rat lung mesenchyme than in homospecific, sub-mandibular mesenchyme. An interaction between epithelium and mesenchyme is involved in the growth of both components in heterotypic recombination.
Effect of substratum and medium
The very limited morphogenesis obtained in heterotypic mouse recombinates cultured on MF over liquid medium suggests that either (or both) substratum or medium interfered with the epithelial-mesenchymal interaction. These possibilities were tested using mouse submandibular epithelium in combination with rat lung mesenchyme since rat mesenchyme is quantitatively more effective than that of mouse on the agar/plasma clot medium. Mesenchyme with an estimated initial protein content equivalent to two submandibular mesenchymes was used throughout. The four combinations agar/plasma clot, agar/liquid medium, MF/plasma clot, and MF/liquid medium, were tested in a (2×2) factorial experiment (A = 20). For the second combination a drop of agar was allowed to gel on the platform of a MF assembly; for the third combination a small piece of MF was placed on the surface of the plasma clot. Homotypic recombinates of submandibular and lung were tested with the first and last combination only.
The results were unequivocal (Figs. 9, 10): submandibular epithelium showed good morphogenesis in lung mesenchyme only when the recombinate was sup-ported by agar, irrespective of the nutrient medium (Figs. 9C, E, 10 A) whereas only meagre budding occurred on MF (Fig. 9D, F). No such differences between agar and MF were found for the homotypic submandibular recombinates (Figs. 9 A, B, 10 B) and there was only a limited, though definite effect (P < 0·001 at 4 and 5 days) on the homotypic lung recombinates (Figs. 9G, H, 10C).
Comparison of cell density in the mesenchyme after 6 days culture (Table 5) showed no significant difference between cell spacing in submandibular mesen-chyme on the two substrata. However, the cells in lung mesenchyme were closely packed when on agar but became diffuse on MF, more so in the hetero-typic than in the homotypic recombinates (P < 0·001).
Effect of initial age of lung mesenchyme
Fourteen-day rat lung is generally more developed than 12-day mouse lung. The possibility that a critical stage exists before which lung mesenchyme is unable to support mouse submandibular morphogenesis was tested in recombinates with 13-day rat lung mesenchyme. Four mesenchymes per recombinate were used compared with two 14-day rat lung or two mouse submandibular mesenchymes. The experiment was set up in three replicates with three samples per treatment combination in each replicate; N = 27.
Effect of trypsin-pancreatin treatment
Although it is not possible to obtain whole epithelial rudiments free of mesenchyme without using enzyme treatment, substantial quantities of mesen-chyme, from both submandibular and lung, can be obtained by dissection and have been used by others in recombination experiments. Two series, trypsinized and dissected mesenchyme from 14-day mouse submandibular gland, 14-day rat lung and 12-day mouse lung were recombined with trypsinized mouse sub-mandibular epithelium in a 2 × 3 factorial experiment in two replicates, with three samples per treatment combination in each replicate; N = 36.
It was found that trypsin-pancreatin treatment of the mesenchyme had no effect on the number of epithelial buds formed compared with dissected mesen-chyme at any stage in any of the recombinates.
Differences between rat and mouse lung mesenchyme
Since rat and mouse lung mesenchyme are not quantitatively equivalent in their ability to support mouse submandibular morphogenesis, and since this difference becomes evident within 3 days of culture, early recombinates were examined histologically for (1) selective necrosis and (2) differences in distribu-tion of acidic glycosaminoglycans, since such substances may play a key role in submandibular morphogeneis (Bernfield & Wessells, 1970; Bernfield & Banerjee, 1972; Bernfield, Banerjee & Cohn, 1972).
Necrotic areas were found within 18 h in lung mesenchyme from both mouse and rat in recombination with their own or mouse submandibular epithelium. Relatively more of the mouse than the rat mesenchyme appeared to be affected ; the necrotic areas were not in contact with the epithelium, but peripheral to the blood vessels (Fig. 2F). Intact lungs that had been treated with trypsin-pancreatin, but not mechanically dissociated, also showed some necrosis in the mesenchyme which was more obvious in the mouse than in the rat material. Intact mouse lungs cultured without prior enzyme treatment occasionally had small necrotic areas; intact rat lungs were healthy. No such necrosis was found in submandibular mesenchyme. After 40 h culture necrotic patches were still present in the mesenchyme of recombinates of mouse submandibular epithelium with mouse lung mesenchyme, but not in any of the other recombinates. At 4 and 6 days the remaining mesenchyme cells appeared healthy.
Alcian blue-staining material with a critical electrolyte concentration of about 0·6 M-MgCl2 was found at the epithelial-mesenchymal interface and inter-cellularly in the mesenchyme in all recombinates and intact explants at 18 h and subsequently. There was no obvious difference between any of the recombinates.
Effect of lung mesenchyme on histogenesis and cytodifferentiation of submandibular epithelium
Mouse submandibular epithelium had formed smaller, more closely packed buds after 5 days in lung mesenchyme than in its own mesenchyme (Fig. 12 A, B). Such submandibular buds in lung mesenchyme were precociously differentiated, as shown by the presence of larger quantities of PAS-positive, amylase-resistant material compared with the homotypic controls (Fig. 12C-E). No such differ-ence was seen in older ‘12-day’ cultures (Fig. 2A-E).
Tubules formed by salivary epithelium in lung mesenchyme stained densely with PAS. Removal of this material with amylase indicates it to be glycogen (Fig. 12F, G). This effect of lung mesenchyme was particularly noticeable in parotid epithelium, since the tubules of the homotypic recombinates only occasionally contained traces of glycogen. The effect was least evident in recombinates with mouse submandibular epithelium since both buds and tubules in homotypic recombinates normally contained glycogen. Quantitative histochemistry has not been attempted.
DISCUSSION
The finding that lung mesenchyme is able to support morphogenesis and cytodifferentiation of rodent salivary epithelium in vitro contradicts previous reports (Grobstein, 1953; Spooner & Wessells, 1972) and makes untenable the hypothesis (Grobstein, 1967) that there is a mesenchyme-specific factor or property unique to salivary mesenchyme and essential for salivary morpho-genesis. The conclusion applies to both submandibular and parotid epithelium from mouse and rat.
Since the direct contradiction was in the response of mouse submandibular epithelium to lung mesenchyme, the factors influencing tissue interaction in this recombinate were examined in more detail, using lung mesenchyme from both mouse and rat. A quantitative difference in the ability of submandibular and lung mesenchyme to support morphogenesis in submandibular epi-thelium was found : the smallest amount of submandibular mesenchyme tested -half that obtained from one 14-day submandibular gland -supported a normal rate of budding, whereas more than twice this mass of 12-day mouse lung mesenchyme was required to evoke a morphogenetic response. Although no minimum effective mass of rat lung mesenchyme was demonstrated, both the number of buds and the volume of submandibular epithelium after 6 days culture were less than in the homotypic controls with the same initial amount of mesenchyme. The accompanying difference in the final number of mesenchyme cells between heterotypic and homotypic lung recombinates implies that lung epithelium is necessary for the maintenance and growth of lung mesenchyme and cannot be adequately replaced by submandibular epithelium. The relative amount of lung mesenchyme influences the growth of bronchial epithelium (Alescio, Cassini & Ladu, 1963; Alescio & Colombo Piperno, 1967; Alescio & Di Michele, 1968); a reciprocal effect of lung epithelium on the growth of lung mesenchyme has not been reported previously, although lung epithelium does influence the differentiation of lung mesenchyme (Taderera, 1967).
Such a requirement of lung mesenchyme for lung epithelium would account for the reduction in size with time of the heterotypic mouse recombinates and their improved development with larger initial masses of lung mesenchyme. Since the picture may be confused by selective necrosis in lung mesenchyme, the possibility of a direct and reciprocal relationship between epithelium and mesenchyme with respect to cell division deserves further investigation.
The quantitative difference between mouse lung and submandibular mesen-chyme in evoking a morphogenetic response from submandibular epithelium could have contributed to Spooner & Wessells’ (1972) negative results, but perhaps not to Grobstein’s (1953): he used 6–8 pieces of mesenchyme of un-defined size per recombinate. The nature of the non-nutrient substratum by which the explants were supported appears to have been the overriding factor: in the present experiments a mass of lung mesenchyme sufficient for supporting substantial submandibular growth and morphogenesis on an agar substratum evoked no, or only a meagre, response on MF. A further experiment with rat lung mesenchyme eliminated the nutrient medium as a source of the difference in response on the two substrata. The substrata used by Spooner & Wessells (MF) and by Grobstein (glass-clot interface) are alike in that they would be expected to encourage mesenchyme spreading. The agar substratum was origin-ally chosen for salivary gland rudiments to repress this tendency in long-term cultures (Lawson, 1970). Mesenchyme spreading could lead to a reduction below the critical mass or critical density necessary for the interaction of a particular mesenchyme with submandibular epithelium. After 6 days culture there was no difference in the spacing of submandibular mesenchyme cells on agar or MF, nor in the number of epithelial buds formed in this mesenchyme on the two substrata; but lung mesenchyme cells, which were closely packed on an agar substratum, became dispersed on MF. This dispersion was greater in the heterotypic recombinates, accompanied by a reduction in bud formation. The slightly closer packing on MF of lung mesenchyme cells in association with their own as against submandibular epithelium could be expected from the proposed growth-promoting action of lung epithelium on lung mesenchyme. If these observations are relevant to processes occurring earlier in the culture period, they imply that submandibular mesenchyme is effective at a lower cell density than lung mesenchyme in supporting branching morphogenesis.
It must be emphasized that the results under discussion concern the behaviour of lung mesenchyme that has been separated from the epithelium prior to recombination : the mesothelium investing the mesenchyme has therefore been extensively disrupted. The epithelium of the intact lung both grows and forms buds less rapidly on agar than directly on the surface of a plasma clot or on MF (unpublished observations).
Lung mesenchyme is not the only non-salivary mesenchyme able to support salivary morphogenesis: Cunha (1972) has shown that mouse submandibular epithelium will undergo extensive development in the mesenchyme of accessory sexual structures when the recombinates are cultivated in the anterior chamber of the eye of adult male mice. He suggests that sensitivity of mesenchyme to androgens is the characteristic determining whether a particular mesenchyme will support the development of salivary epithelium. If this explanation is appropriate for the interaction of submandibular epithelium with lung mesen-chyme in vitro it must be assumed that (1) the 10% embryo extract and 10% foetal calf serum used in combination with Ham’s F12 medium contained suf-ficient androgen to initiate the interaction (Eagle’s basal medium plus 10% foetal calf serum contains no effective androgen (Cunha, 1973)); (2) F12 plus 10 % foetal calf serum plus 10 % embryo extract contains the same effective level of androgen as 66 % cock plasma plus 33 % embryo extract; (3) the interaction of lung epithelium with lung mesenchyme occurs via a different, non-androgen-sensitive mechanism. Alternatively, it is conceivable that foetal submandibular and lung mesenchyme can support the development of submandibular epi-thelium without mediation by androgens, whereas that from urogenital sinus or prostate can only do so in an androgen-containing environment. This does not necessarily imply that the basic mechanism is different.
A mechanism for salivary morphogenesis has been proposed (Bernfield & Wessells, 1970; Spooner &Wessells, 1970; Bernfield & Banerjee, 1972; Bernfield et al. 1972; Spooner & Wessells, 1972; Ash, Spooner & Wessells, 1973) in which epithelial clefts, which determine the branching points of the developing epithelial tree, are formed by the contraction of basal microfilaments in the epithelium. The conditions for cleft initiation are thought to be created by the deposition of proteoglycans and collagen at the epithelial-mesenchymal interface, for which mesenchyme is required. Lung epithelium characteristically does not form clefts, the change in contour of the epithelium at a branching point being much less sharp. It is noteworthy that submandibular epithelium, after initially forming large, flat buds in lung mesenchyme, then produces further buds peripherally by cleft formation. The materials present at the epithelial-mesenchymal interface in these recombinates, as well as in normal lung, clearly require further investigation.
The precocious appearance of PAS-positive material in submandibular buds formed in lung mesenchyme is accompanied by their closer packing and smaller size and the presence of a lumen. It is not known whether any of these factors are necessary or contingent for cytodifferentiation. The enhanced amount of glycogen, particularly in the tubular epithelium, is reminiscent of the large pools of glycogen normally present in morphogenetically active bronchial epi-thelium (Sorokin, Padykula & Herman, 1959; Sorokin, 1961; Alescio & Dani, 1971). However, there are reasons for thinking that the situation in the hetero-typic recombinate is not analogous to that in lung, where the presence of epi-thelial glycogen is closely related to the morphogenetic activity of the epithelium : first, small amounts of glycogen are normally present in salivary tubular epi-thelium at some stages in vitro′, secondly, the tubular epithelium is no longer forming new buds; thirdly, substantial quantities of glycogen were produced in the tubular epithelium of heterotypic recombinates cultured on MF, even when buds were few or absent. An alternative explanation is to suppose that salivary tubular epithelium will normally store glycogen unless restrained. Such a re-straint could be provided by glycogenolytic agents in salivary mesenchyme, e.g. norepinephrine in association with the ganglion in the stalk region (Ash et al. 1973): nerve cells are present in cultured submandibular mesenchyme but have not been found in cultured foetal lung (J. Bluemink, personal communication). Another possibility is the hypothetical presence in salivary mesenchyme of special catecholamine-containing cells whose secretion could influence the neighbouring epithelium, as has been found in chick kidney mesenchyme cultured in combination with liver endoderm (Le Douarin & Houssaint, 1969; Le Douarin, 1971).
ACKNOWLEDGEMENTS
It is a pleasure to thank Miss B. M. van der Have for her skilled technical assistance, L. Boom for photographic work and Dr J. Faber for criticizing the manuscript.
Note added in proof
W. D. Ball (J. exp. Zool. (1974) 188, 277-288) has reported that rat submandibular epithelium undergoes limited morphogenesis in lung mesenchyme when cultured at a plastic-clot interface. The results are similar to those described here for mouse submandibular epithelium in rat lung mesenchyme on MF. In contrast, in Ball’s culture system the morphogenesis of rat sublingual epithelium in lung mesenchyme approached that of the controls.