Sala, N. L. & Freire, F. Relationship between ultrastructure and response to oxytocin of the mammary myoepithelium throughout pregnancy and lactation: effect of estrogen and progesterone. Biol. Reprod. 11, 7-17 (1974).
Gimpl, G. & Fahrenholz, F. The oxytocin receptor system: structure, function, and regulation. Physiol. Rev. 81, 629-683 (2001).
Graf, G. C. Ejection of milk in relation to levels of oxytocin injected intramuscularly. J. Dairy Sci. 52, 1003-1007 (1969).
Sala, N. L., Luther, E. C., Arballo, J. C. & Cordero Funes, J. C. Oxytocin reproducing reflex milk ejection in lactating women. J. Appl. Physiol. 36, 154-158 (1974).
Wakerley, J. B., Dyball, R. E. & Lincoln, D. W. Milk ejection in the rat: the result of a selective release of oxytocin. J. Endocrinol. 57, 557-558 (1973).
Carter, C. S. Neuroendocrine perspectives on social attachment and love. Psychoneuroendocrinology 23, 779-818 (1998).
Nakajima, M., Gorlich, A. & Heintz, N. Oxytocin Modulates Female Sociosexual Behavior through a Specific Class of Prefrontal Cortical Interneurons. Cell 159, 295-305 (2014).
Kosfeld, M., Heinrichs, M., Zak, P. J., Fischbacher, U. & Fehr, E. Oxytocin increases trust in humans. Nature 435, 673-676 (2005).
Jin, D. et al. CD38 is critical for social behaviour by regulating oxytocin secretion. Nature 446, 41-45 (2007).
Elabd, C. et al. Oxytocin controls differentiation of human mesenchymal stem cells and reverses osteoporosis. Stem cells 26, 2399-2407 (2008).
Kim, Y. S. et al. Priming of mesenchymal stem cells with oxytocin enhances the cardiac repair in ischemia/reperfusion injury. Cells Tissues Organs 195, 428-442 (2012).
Elabd, C. et al. Oxytocin is an age-specific circulating hormone that is necessary for muscle maintenance and regeneration. Nat. Commun. 5, 4082 (2014).
Monstein, H. J., Grahn, N., Truedsson, M. & Ohlsson, B. Oxytocin and oxytocin-receptor mRNA expression in the human gastrointestinal tract: a polymerase chain reaction study. Regul. Pept. 119, 39-44 (2004).
Welch, M. G. et al. Expression and developmental regulation of oxytocin (OT) and oxytocin receptors (OTR) in the enteric nervous system (ENS) and intestinal epithelium. J. Comp. Neurol. 512, 256-270 (2009).
Yu, Q. et al. Oxytocin is expressed by both intrinsic sensory and secretomotor neurons in the enteric nervous system of Guinea pig. Cell Tissue Res. 344, 227-237 (2011).
Welch, M. G., Margolis, K. G., Li, Z. & Gershon, M. D. Oxytocin regulates gastrointestinal motility, inflammation, macromolecular permeability, and mucosal maintenance in mice. Am. J. Physiol. Gastrointest. Liver Physiol. 307, G848-862 (2014).
Halm, D. R. & Halm, S. T. Prostanoids stimulate K secretion and Cl secretion in Guinea pig distal colon via distinct pathways. Am. J. Physiol. Gastrointest. Liver Physiol. 281, G984-996 (2001).
Unmack, M. A., Rangachari, P. K. & Skadhauge, E. Effects of isoprostanes and prostanoids on porcine small intestine. J. Pharmacol. Exp. Ther. 296, 434-441 (2001).
Williams, C. S. & DuBois, R. N. Prostaglandin endoperoxide synthase: why two isoforms? Am. J. Physiol. 270, G393-400 (1996).
Dubois, R. N. et al. Cyclooxygenase in biology and disease. FASEB J. 12, 1063-1073 (1998).
Paliege, A. et al. Inhibition of nNOS expression in the macula densa by COX-2-derived prostaglandin E(2). Am. J. Physiol. Renal Physiol. 287, F152-159 (2004).
MacNaughton, W. K. & Cushing, K. Role of constitutive cyclooxygenase-2 in prostaglandin-dependent secretion in mouse colon in vitro. J. Pharmacol. Exp. Ther. 293, 539-544 (2000).
Yasojima, K., Schwab, C., McGeer, E. G. & McGeer, P. L. Distribution of cyclooxygenase-1 and cyclooxygenase-2 mRNAs and proteins in human brain and peripheral organs. Brain Res. 830, 226-236 (1999).
McAdam, B. F. et al. Systemic biosynthesis of prostacyclin by cyclooxygenase (COX)-2: the human pharmacology of a selective inhibitor of COX-2. Proc. Natl Acad. Sci. USA 96, 272-277 (1999).
Helliwell, R. J., Adams, L. F. & Mitchell, M. D. Prostaglandin synthases: recent developments and a novel hypothesis. Prostaglandins Leukot. Essent. Fatty Acids 70, 101-113 (2004).
Hawkey, C. J. & Rampton, D. S. Prostaglandins and the gastrointestinal mucosa: are they important in its function, disease, or treatment? Gastroenterology 89, 1162-1188 (1985).
Morimoto, K. et al. Cellular localization of mRNAs for prostaglandin E receptor subtypes in mouse gastrointestinal tract. Am. J. Physiol. 272, G681-687 (1997).
Takeuchi, K. et al. Prostaglandin E receptor subtypes involved in stimulation of gastroduodenal bicarbonate secretion in rats and mice. J. Physiol. Pharmacol. 50, 155-167 (1999).
Field, M., Musch, M. W. & Stoff, J. S. Role of prostaglandins in the regulation of intestinal electrolyte transport. Prostaglandins 21 Suppl, 73-79 (1981).
Hinterleitner, T. A. & Powell, D. W. Immune system control of intestinal ion transport. Proc. Soc. Exp. Biol. Med. 197, 249-260 (1991).
Burghardt, R. C., Barhoumi, R., Sanborn, B. M. & Andersen, J. Oxytocin-induced Ca2+ responses in human myometrial cells. Biol. Reprod. 60, 777-782 (1999).
Barhoumi, R., Mouneimne, Y., Phillips, T. D., Safe, S. H. & Burghardt, R. C. Alteration of oxytocin-induced calcium oscillations in clone 9 cells by toxin exposure. Fundam. Appl. Toxicol. 33, 220-228 (1996).
Satoh, Y., Habara, Y., Ono, K. & Kanno, T. Carbamylcholine- and catecholamine-induced intracellular calcium dynamics of epithelial cells in mouse ileal crypts. Gastroenterology 108, 1345-1356 (1995).
Zonta, M. et al. Glutamate-mediated cytosolic calcium oscillations regulate a pulsatile prostaglandin release from cultured rat astrocytes. J. Physiol. 553, 407-414 (2003).
Wouters, E., Hudson, C. A., McArdle, C. A. & Bernal, A. L. Central role for protein kinase C in oxytocin and epidermal growth factor stimulated cyclooxygenase 2 expression in human myometrial cells. BMC Res. Notes 7, 357 (2014).
Lin, C. C. et al. Upregulation of COX-2/PGE2 by ET-1 mediated through Ca2+ -dependent signals in mouse brain microvascular endothelial cells. Mol. Neurobiol. 49, 1256-1269 (2014).
North, T. E. et al. Prostaglandin E2 regulates vertebrate haematopoietic stem cell homeostasis. Nature 447, 1007-1011 (2007).
Kleiveland, C. R., Kassem, M. & Lea, T. Human mesenchymal stem cell proliferation is regulated by PGE2 through differential activation of cAMP-dependent protein kinase isoforms. Exp. Cell. Res. 314, 1831-1838 (2008).
Goessling, W. et al. Genetic interaction of PGE2 and Wnt signaling regulates developmental specification of stem cells and regeneration. Cell 136, 1136-1147 (2009).
Hanson, W. R. & Thomas, C. 16, 16-dimethyl prostaglandin E2 increases survival of murine intestinal stem cells when given before photon radiation. Radiat. Res. 96, 393-398 (1983).
Cohn, S. M., Schloemann, S., Tessner, T., Seibert, K. & Stenson, W. F. Crypt stem cell survival in the mouse intestinal epithelium is regulated by prostaglandins synthesized through cyclooxygenase-1. J. Clin. Invest. 99, 1367-1379 (1997).
Crosnier, C., Stamataki, D. & Lewis, J. Organizing cell renewal in the intestine: stem cells, signals and combinatorial control. Nat. Rev. Genet. 7, 349-359 (2006).
Hanson, W. R. & Ainsworth, E. J. 16,16-Dimethyl prostaglandin E2 induces radioprotection in murine intestinal and hematopoietic stem cells. Radiat. Res. 103, 196-203 (1985).
Riehl, T., Cohn, S., Tessner, T., Schloemann, S. & Stenson, W. F. Lipopolysaccharide is radioprotective in the mouse intestine through a prostaglandin-mediated mechanism. Gastroenterology 118, 1106-1116 (2000).
Olsen Hult, L. T., Kleiveland, C. R., Fosnes, K., Jacobsen, M. & Lea, T. EP receptor expression in human intestinal epithelium and localization relative to the stem cell zone of the crypts. PLoS One 6, e26816 (2011).
Eckmann, L. et al. Role of intestinal epithelial cells in the host secretory response to infection by invasive bacteria. Bacterial entry induces epithelial prostaglandin h synthase-2 expression and prostaglandin E2 and F2alpha production. J. Clin. Invest. 100, 296-309 (1997).
Aoyagi, Y. et al. Peroxisome proliferator-activated receptor gamma 2 mutation may cause a subset of ulcerative colitis. Pediatr. Int. 52, 729-734 (2010).
Petersson, J. et al. Importance and regulation of the colonic mucus barrier in a mouse model of colitis. Am. J. Physiol. Gastrointest. Liver Physiol. 300, G327-333 (2011).
Withers, H. R. & Elkind, M. M. Microcolony survival assay for cells of mouse intestinal mucosa exposed to radiation. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 17, 261-267 (1970).
Sato, T. et al. Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche. Nature 459, 262-265 (2009).
