Abstract
Entero-endocrine cells are scattered within the epithelia throughout the whole gastrointestinal
tract, showing remarkable accumulations in the pyloric region and the duodenum. By
light microscopical means these cells and their specific secretion granules respectively
can be demonstrated by numerous staining methods (about 100), in which the argyrophilic
reaction (according to Grimelius) is mainly applied today. Histochemical methods for
the demonstration of entero-endocrine cells are based on the histochemical fluorescent
demonstration of biogenic monoamines (endogenous occurrence or following exogenous
application of amine precursor substances) and on the immunocytochemical demonstration
of gastrointestinal polypeptide hormones. Most of the endocrine cell types (about
16) are responsible for the synthesis of certain enteric hormones. Furthermore, some
entero-endocrine cells may synthesize more than one peptide hormone. Moreover, it
is remarkable that some polypeptides (e.g. Gastrin, Cholecystokinin-Pancreozymin,
Neurotensin, Endorphin, Enkephalin, ACTH) may occur simultaneously in the central
nervous system and in the gastrointestinal tract. Ultrastructurally, entero-endocrine
cells in their entirety mainly exhibit a pale cytoplasm, well developed microvilli
and specific secretion granules varying in shape, size and electron density within
different cell types.
With respect to their mode of function, entero-endocrine cells have also been tentatively
described as modified "sensory cells". The hormones of these cells may accordingly
be interpreted as equivalents of neurotransmitter substances. Morphological investigations
suggest that entero-endocrine cells are controlled by chemical and physical stimuli
including those due to the composition of the chyme in the gut lumen. The enteric
hormones can either directly influence the environment by a "paracrinous" route or
can also effect "target organs" by an "endocrinous" pathway. The enteroendocrine cells
are summed up, together with similar cells of the pancreas and bile duct system as
gastro-entero-pancreatic endocrine cells (GEP-endocrine system). Furthermore, cytochemical
characteristics of many cells in different organs have lead to the definition of the
"APUD cell series" (Pearse 1969). According also to functional aspects, the entero-
endocrine ceils are members of the so-called "paraneurons" (Fujita 1977). The progenitor
cells of entero-endocrine cells have been claimed to originate from the neural crest,
the neural ridge or the neurectoderm respectively. The final proof of this hypothesis
is, however, still lacking. Concerning the differentiation and cell cycle of entero-endocrine
cells, little knowledge dealing with these problems is actually available.
1 Supported by the Deutsche Forschungsgemeinschaft, Grants Fo 77/7 and SFB 87/D 10