Figure 1.
MC are densely represented in the swine snout.
MCs labeled by CK20 immunostaining (in red) appear abundant in the basal layer of the epidermis of swine snout. Conversely, less than 50 MCs/mm2 were found in human glabrous skin. Nuclei were stained in blue with DAPI. (Scale bar, 50 µm).
Figure 2.
Immunofluorescence on selected Merkel cells in culture.
(a) After enrichment, an average of 62% (±3.5) MCs was obtained over 10 experiments as demonstrated by immunostaining using anti-CK20 antibodies and DAPI as a counterstain. In order to define a suitable culture medium for MCs, cells were stimulated by various factors and the morphology of MCs was analyzed by CK20 immunofluorescence. Using DMEM/F12 as a basal medium, neither EGF (20 ng/mL), RA (0.5 µM) or Dexa (1 µM) supported the spreading of MCs. Similarly, neither NGF (100 ng/mL), BDNF (25 ng/mL), NT-3 (25 ng/mL) or the three factors together (b) stimulated the growth of cytoplasmic extensions. (c) Conversely, MCs reacted to bFGF (20 ng/mL), as they extended cytoplasmic outgrowths (arrows), suggesting that this factor acts as a growth factor for MCs. (Scale bar in all pictures, 50 µm).
Figure 3.
Electron microscopy analysis confirmed the identity of Merkel cells.
Ultrastructural analyses were carried out on cells from the enriched MC fraction. (a, b) Up to half of the cells presented features characteristic of MCs: a polylobulated nucleus with numerous typical dense-core granules in a clear cytoplasm. (c) The thin membrane distinguishable around the darkest cytoplasmic granules is consistent with neuroendocrine cells. (Scale bar in a, 5 µm; in b, 2 µm; in c, 500 nm).
Figure 4.
MCs developed cytoplasmic processes when cultured in the presence of serum.
Strikingly, in these culture conditions, stacking of more than five MCs was observed (a, b) and confirmed by CK20 immunofluorescence (c). Interestingly, this stacking is similar to configurations observed in mechanosensitive areas in the touch pads of rats, as demonstrated by CK20 immunostaining in dissociated epidermal layers (d). The meaning of these alignments to the role of MCs remains to be defined. (Scale bars, 10 µm).
Figure 5.
Merkel cells proliferated in culture.
Double immunofluorescence assay using antibodies against CK20 (red) and Ki-67 antigen (green) revealed the ability of MCs to proliferate in vitro. Dividing CK20-positive cells were clearly visible, and all phases of the cell cycle were observed: prophase (a), metaphase (b), anaphase (c, e) and telophase (d, e). (Scale bars, 20 µm).
Figure 6.
Merkel cells produced VIP in culture.
In our culture conditions, MCs produced the neuropeptide VIP as demonstrated by double immunofluorescence using antibodies against CK20 (red) and VIP (green). The production of VIP was confirmed by western blot analysis (WB). (Scale bar, 50 µm).
Figure 7.
Percentage of VIP released by Merkel cells.
The amount of VIP released in the culture supernatant, assessed by ELISA and expressed as a percentage of the control conditions (DMEM/F12 containing 1 mM Ca2+). Exposure to the TRPV4 agonist 4αPDD (1 µM) or histamine (100 µM) stimulated VIP release from MCs. This release was not inhibited by pre-incubation with the Ca2+ channel inhibitor RR (1 µM), indicating a Ca2+-independent pathway. The marked increase of VIP release obtained following stimulation by 4αPDD in a Ca2+-free buffer confirmed these results. In addition, exposure to the neurotransmitter Ach (10 µM) significantly inhibited the amount of VIP released in the presence of Ca2+. This inhibition was suppressed by pre-incubation with RR (1 µM), suggesting the involvement of Ca2+ channels (n = 4, difference significant at P≤0.025.).
Figure 8.
Ca2+ and Ach decreased the release of VIP.
Effect of Ach and Ca2+ on VIP release expressed in ng/well. MCs were cultured in Ca2+-free MEME and then exposed to Ach (100 µM), Ca2+ (1 mM), or both. In the absence of Ca2+, the addition of Ach failed to significantly decrease VIP exocytosis (P>0.1). A lower amount of VIP release was observed in the presence of Ca2+ (1 mM). Finally, the inhibitory effect of Ach on VIP release required extracellular Ca2+ (P≤0.025). These results are consistent with inhibition via Ca2+ channels, probably via muscarinic M2 or M4 Ach receptors.