References
Adashi, E. Y. (1990
).
The potential relevance of cytokines to ovarian physiology: the emerging role of resident ovarian cells of the white blood cell series.
Endocr. Rev. 11, 454–464.
|
CrossRef |
CAS |
PubMed |
Al-Zi’abi, M. O., Fraser, H. M., and Watson, E. D. (2002
).
Cell death during natural and induced luteal regression in mares.
Reproduction 123, 67–77.
|
CrossRef |
CAS |
PubMed |
Ancelin, M., Chollet-Martin, S., Herve, M. A., Legrand, C., El Benna, J., and Perrot-Applanat, M. (2004
).
Vascular endothelial growth factor VEGF189 induces human neutrophil chemotaxis in extravascular tissue via an autocrine amplification mechanism.
Lab. Invest. 84, 502–512.
|
CrossRef |
CAS |
PubMed |
Ardi, V. C., Van den Steen, P. E., Opdenakker, G., Schweighofer, B., Deryugina, E. I., and Quigley, J. P. (2009
).
Neutrophil MMP-9 proenzyme, unencumbered by TIMP-1, undergoes efficient activation
in vivo and catalytically induces angiogenesis via a basic fibroblast growth factor (FGF-2)/FGFR-2 pathway.
J. Biol. Chem. 284, 25 854–25 866.
|
CrossRef |
CAS |
Aust, G., Simchen, C., Heider, U., Hmeidan, F. A., Blumenauer, V., and Spanel-Borowski, K. (2000
).
Eosinophils in the human corpus luteum: the role of RANTES and eotaxin in eosinophil attraction into periovulatory structures.
Mol. Hum. Reprod. 6, 1085–1091.
|
CrossRef |
CAS |
PubMed |
Bauer, M., Reibiger, I., and Spanel-Borowski, K. (2001
).
Leucocyte proliferation in the bovine corpus luteum.
Reproduction 121, 297–305.
|
CrossRef |
CAS |
PubMed |
Bausch, D., Pausch, T., Krauss, T., Hopt, U. T., Fernandez-del-Castillo, C., Warshaw, A. L., Thayer, S. P., and Keck, T. (2011
).
Neutrophil granulocyte derived MMP-9 is a VEGF independent functional component of the angiogenic switch in pancreatic ductal adenocarcinoma.
Angiogenesis 14, 235–243.
|
CrossRef |
CAS |
PubMed |
Best, C. L., Pudney, J., Welch, W. R., Burger, N., and Hill, J. A. (1996
).
Localization and characterization of white blood cell populations within the human ovary throughout the menstrual cycle and menopause.
Hum. Reprod. 11, 790–797.
|
CrossRef |
CAS |
PubMed |
Brännström, M., and Friden, B. (1997
).
Immune regulation of corpus luteum function.
Semin. Reprod. Endocrinol. 15, 363–370.
|
CrossRef |
PubMed |
Brannstrom, M., and Norman, R. J. (1993
).
Involvement of leukocytes and cytokines in the ovulatory process and corpus luteum function.
Hum. Reprod. 8, 1762–1775.
|
CAS |
PubMed |
Brännström, M., Giesecke, L., Moore, I. C., van den Heuvel, C. J., and Robertson, S. A. (1994a
).
Leukocyte subpopulations in the rat corpus luteum during pregnancy and pseudopregnancy.
Biol. Reprod. 50, 1161–1167.
|
CrossRef |
PubMed |
Brannstrom, M., Pascoe, V., Norman, R. J., and McClure, N. (1994b
).
Localization of leukocyte subsets in the follicle wall and in the corpus luteum throughout the human menstrual cycle.
Fertil. Steril. 61, 488–495.
|
CAS |
PubMed |
Brännström, M., Bonello, N., Norman, R. J., and Robertson, S. A. (1995
).
Reduction of ovulation rate in the rat by administration of a neutrophil-depleting monoclonal antibody.
J. Reprod. Immunol. 29, 265–270.
|
CrossRef |
PubMed |
Brown, H. M., Robker, R. L., and Russell, D. L. (2010
).
Development and hormonal regulation of the ovarian lymphatic vasculature.
Endocrinology 151, 5446–5455.
|
CrossRef |
CAS |
PubMed |
Bukovský, A., Presl, J., Krabec, Z., and Bednarik, T. (1977
).
Ovarian function in adult rats treated with antithymocyte serum.
Experientia 33, 280–281.
|
CrossRef |
PubMed |
Bukulmez, O., and Arici, A. (2000
).
Leukocytes in ovarian function.
Hum. Reprod. Update 6, 1–15.
|
CrossRef |
CAS |
PubMed |
Cavender, J. L., and Murdoch, W. J. (1988
).
Morphological studies of the microcirculatory system of periovulatory ovine follicles.
Biol. Reprod. 39, 989–997.
|
CrossRef |
CAS |
PubMed |
Chang, R. J., Gougeon, A., and Erickson, G. F. (1998
).
Evidence for a neutrophil–interleukin-8 system in human folliculogenesis.
Am. J. Obstet. Gynecol. 178, 650–657.
|
CrossRef |
CAS |
PubMed |
Coffelt, S. B., Hughes, R., and Lewis, C. E. (2009
).
Tumor-associated macrophages: effectors of angiogenesis and tumor progression.
Biochim. Biophys. Acta 1796, 11–18.
|
CAS |
PubMed |
Coussens, L. M., Tinkle, C. L., Hanahan, D., and Werb, Z. (2000
).
MMP-9 supplied by bone marrow-derived cells contributes to skin carcinogenesis.
Cell 103, 481–490.
|
CrossRef |
CAS |
PubMed |
Cursiefen, C., Chen, L., Borges, L. P., Jackson, D., Cao, J., Radziejewski, C., D’Amore, P. A., Dana, M. R., Wiegand, S. J., and Streilein, J. W. (2004
).
VEGF-A stimulates lymphangiogenesis and hemangiogenesis in inflammatory neovascularization via macrophage recruitment.
J. Clin. Invest. 113, 1040–1050.
|
CrossRef |
CAS |
PubMed |
Dadras, S. S., Paul, T., Bertoncini, J., Brown, L. F., Muzikansky, A., Jackson, D. G., Ellwanger, U., Garbe, C., Mihm, M. C., and Detmar, M. (2003
).
Tumor lymphangiogenesis: a novel prognostic indicator for cutaneous melanoma metastasis and survival.
Am. J. Pathol. 162, 1951–1960.
|
CrossRef |
PubMed |
Emi, N., Kanzaki, H., Yoshida, M., Takakura, K., Kariya, M., Okamoto, N., Imai, K., and Mori, T. (1991
).
Lymphocytes stimulate progesterone production by cultured human granulosa luteal cells.
Am. J. Obstet. Gynecol. 165, 1469–1474.
|
CAS |
PubMed |
Farin, C. E., Moeller, C. L., Sawyer, H. R., Gamboni, F., and Niswender, G. D. (1986
).
Morphometric analysis of cell types in the ovine corpus luteum throughout the estrous cycle.
Biol. Reprod. 35, 1299–1308.
|
CrossRef |
CAS |
PubMed |
Fridlender, Z. G., Sun, J., Kim, S., Kapoor, V., Cheng, G., Ling, L., Worthen, G. S., and Albelda, S. M. (2009
).
Polarization of tumor-associated neutrophil phenotype by TGF-beta: ‘N1’ versus ‘N2’ TAN.
Cancer Cell 16, 183–194.
|
CrossRef |
CAS |
PubMed |
Gaytan, F., Morales, C., Garcia-Pardo, L., Reymundo, C., Bellido, C., and Sanchez-Criado, J. E. (1998
).
Macrophages, cell proliferation, and cell death in the human menstrual corpus luteum.
Biol. Reprod. 59, 417–425.
|
CrossRef |
CAS |
PubMed |
Good, D. J., Polverini, P. J., Rastinejad, F., Le Beau, M. M., Lemons, R. S., Frazier, W. A., and Bouck, N. P. (1990
).
A tumor suppressor-dependent inhibitor of angiogenesis is immunologically and functionally indistinguishable from a fragment of thrombospondin.
Proc. Natl Acad. Sci. USA 87, 6624–6628.
|
CrossRef |
CAS |
PubMed |
Gordon, S. (2003
).
Alternative activation of macrophages.
Nat. Rev. Immunol. 3, 23–35.
|
CrossRef |
CAS |
PubMed |
Gospodarowicz, D., Cheng, J., Lui, G. M., Baird, A., Esch, F., and Bohlen, P. (1985
).
Corpus luteum angiogenic factor is related to fibroblast growth factor.
Endocrinology 117, 2383–2391.
|
CrossRef |
CAS |
PubMed |
Goto, J., Suganuma, N., Takata, K., Kitamura, K., Asahina, T., Kobayashi, H., Muranaka, Y., Furuhashi, M., and Kanayama, N. (2002
).
Morphological analyses of interleukin-8 effects on rat ovarian follicles at ovulation and luteinization
in vivo.
Cytokine 20, 168–173.
|
CrossRef |
CAS |
PubMed |
Halme, J., Hammond, M. G., Syrop, C. H., and Talbert, L. M. (1985
).
Peritoneal macrophages modulate human granulosa-luteal cell progesterone production.
J. Clin. Endocrinol. Metab. 61, 912–916.
|
CrossRef |
CAS |
PubMed |
Hein, W. R., Shelton, J. N., Simpson-Morgan, M. W., Seamark, R. F., and Morris, B. (1988
).
Flow and composition of lymph from the ovary and uterus of cows during pregnancy.
J. Reprod. Fertil. 83, 309–323.
|
CrossRef |
CAS |
PubMed |
Heishi, T., Hosaka, T., Suzuki, Y., Miyashita, H., Oike, Y., Takahashi, T., Nakamura, T., Arioka, S., Mitsuda, Y., Takakura, T., Hojo, K., Matsumoto, M., Yamauchi, C., Ohta, H., Sonoda, H., and Sato, Y. (2010
).
Endogenous angiogenesis inhibitor vasohibin1 exhibits broad-spectrum antilymphangiogenic activity and suppresses lymph node metastasis.
Am. J. Pathol. 176, 1950–1958.
|
CrossRef |
CAS |
PubMed |
Heryanto, B., Girling, J. E., and Rogers, P. A. (2004
).
Intravascular neutrophils partially mediate the endometrial endothelial cell proliferative response to oestrogen in ovariectomised mice.
Reproduction 127, 613–620.
|
CrossRef |
CAS |
PubMed |
Hosaka, T., Kimura, H., Heishi, T., Suzuki, Y., Miyashita, H., Ohta, H., Sonoda, H., Moriya, T., Suzuki, S., Kondo, T., and Sato, Y. (2009
).
Vasohibin-1 expression in endothelium of tumor blood vessels regulates angiogenesis.
Am. J. Pathol. 175, 430–439.
|
CrossRef |
PubMed |
Hurwitz, A., Payne, D. W., Packman, J. N., Andreani, C. L., Resnick, C. E., Hernandez, E. R., and Adashi, E. Y. (1991
).
Cytokine-mediated regulation of ovarian function: interleukin-1 inhibits gonadotropin-induced androgen biosynthesis.
Endocrinology 129, 1250–1256.
|
CrossRef |
CAS |
PubMed |
Ichikawa, S., Uchino, S., and Hirata, Y. (1987
).
Lymphatic and blood vasculature of the forming corpus luteum.
Lymphology 20, 73–83.
|
CAS |
PubMed |
Imakawa, K., Anthony, R. V., Kazemi, M., Marotti, K. R., Polites, H. G., and Roberts, R. M. (1987
).
Interferon-like sequence of ovine trophoblast protein secreted by embryonic trophectoderm.
Nature 330, 377–379.
|
CrossRef |
CAS |
PubMed |
Jiemtaweeboon, S., Shirasuna, K., Nitta, A., Kobayashi, A., Schuberth, H. J., Shimizu, T., and Miyamoto, A. (2011
).
Evidence that polymorphonuclear neutrophils infiltrate into the developing corpus luteum and promote angiogenesis with interleukin-8 in the cow.
Reprod. Biol. Endocrinol. 9, 79.
|
CAS |
PubMed |
Joukov, V., Sorsa, T., Kumar, V., Jeltsch, M., Claesson-Welsh, L., Cao, Y., Saksela, O., Kalkkinen, N., and Alitalo, K. (1997
).
Proteolytic processing regulates receptor specificity and activity of VEGF-C.
EMBO J. 16, 3898–3911.
|
CrossRef |
CAS |
PubMed |
Karkkainen, M. J., Haiko, P., Sainio, K., Partanen, J., Taipale, J., Petrova, T. V., Jeltsch, M., Jackson, D. G., Talikka, M., Rauvala, H., Betsholtz, C., and Alitalo, K. (2004
).
Vascular endothelial growth factor C is required for sprouting of the first lymphatic vessels from embryonic veins.
Nat. Immunol. 5, 74–80.
|
CrossRef |
CAS |
PubMed |
Kimura, Y. N., Watari, K., Fotovati, A., Hosoi, F., Yasumoto, K., Izumi, H., Kohno, K., Umezawa, K., Iguchi, H., Shirouzu, K., Takamori, S., Kuwano, M., and Ono, M. (2007
).
Inflammatory stimuli from macrophages and cancer cells synergistically promote tumor growth and angiogenesis.
Cancer Sci. 98, 2009–2018.
|
CrossRef |
CAS |
PubMed |
Kliem, H., Welter, H., Kraetzl, W. D., Steffl, M., Meyer, H. H., Schams, D., and Berisha, B. (2007
).
Expression and localisation of extracellular matrix degrading proteases and their inhibitors during the oestrous cycle and after induced luteolysis in the bovine corpus luteum.
Reproduction 134, 535–547.
|
CrossRef |
CAS |
PubMed |
Kobayashi, S., Berisha, B., Amselgruber, W. M., Schams, D., and Miyamoto, A. (2001
).
Production and localisation of angiotensin II in the bovine early corpus luteum: a possible interaction with luteal angiogenic factors and prostaglandin F2 alpha.
J. Endocrinol. 170, 369–380.
|
CrossRef |
CAS |
PubMed |
Kobayashi, S., Acosta, T. J., Hayashi, K., Berisha, B., Ozawa, T., Ohtani, M., Schams, D., and Miyamoto, A. (2002
).
Intraluteal release of prostaglandin F
2alpha and E
2 during corpora lutea development in the cow.
J. Reprod. Dev. 48, 583–590.
|
CrossRef |
CAS |
Koch, A. E., Polverini, P. J., Kunkel, S. L., Harlow, L. A., DiPietro, L. A., Elner, V. M., Elner, S. G., and Strieter, R. M. (1992
).
Interleukin-8 as a macrophage-derived mediator of angiogenesis.
Science 258, 1798–1801.
|
CrossRef |
CAS |
PubMed |
Komatsu, K., Manabe, N., Kiso, M., Shimabe, M., and Miyamoto, H. (2003
).
Changes in localization of immune cells and cytokines in corpora lutea during luteolysis in murine ovaries.
J. Exp. Zoolog. A Comp. Exp. Biol. 296, 152–159.
Liclican, E. L., Nguyen, V., Sullivan, A. B., and Gronert, K. (2010
).
Selective activation of the prostaglandin E
2 circuit in chronic injury-induced pathologic angiogenesis.
Invest. Ophthalmol. Vis. Sci. 51, 6311–6320.
|
CrossRef |
PubMed |
Lobel, B. L., and Levy, E. (1968
).
Enzymic correlates of development, secretory function and regression of follicles and corpora lutea in the bovine ovary.
Acta Endocrinol. 59, S35–S51.
Loeb, L. (1906
).
The formation of the corpus luteum in the guinea pig.
J. Am. Med. Assoc. XLVI, 416–423.
|
CrossRef |
Maruyama, K., Ii, M., Cursiefen, C., Jackson, D. G., Keino, H., Tomita, M., Van Rooijen, N., Takenaka, H., D’Amore, P. A., Stein-Streilein, J., Losordo, D. W., and Streilein, J. W. (2005
).
Inflammation-induced lymphangiogenesis in the cornea arises from CD11b-positive macrophages.
J. Clin. Invest. 115, 2363–2372.
|
CrossRef |
CAS |
PubMed |
Matsuyama, S., and Takahashi, M. (1995
).
Immunoreactive (ir)-transforming growth factor (TGF)-beta in rat corpus luteum: ir-TGF beta is expressed by luteal macrophages.
Endocr. J. 42, 203–217.
|
CrossRef |
CAS |
PubMed |
McCracken, J. A., Schramm, W., Barcikowski, B., and Wilson, L. (1981
).
The identification of prostaglandin F2 alpha as a uterine luteolytic hormone and the hormonal control of its synthesis.
Acta Vet. Scand. Suppl. 77, 71–88.
|
CAS |
PubMed |
Meyer, M. D., Hansen, P. J., Thatcher, W. W., Drost, M., Badinga, L., Roberts, R. M., Li, J., Ott, T. L., and Bazer, F. W. (1995
).
Extension of corpus luteum lifespan and reduction of uterine secretion of prostaglandin F2 alpha of cows in response to recombinant interferon-tau.
J. Dairy Sci. 78, 1921–1931.
|
CrossRef |
CAS |
PubMed |
Miyamoto, A., Shirasuna, K., and Sasahara, K. (2009
).
Local regulation of corpus luteum development and regression in the cow: impact of angiogenic and vasoactive factors.
Domest. Anim. Endocrinol. 37, 159–169.
|
CrossRef |
CAS |
PubMed |
Moor, R. M., Hay, M. F., and Seamark, R. F. (1975
).
The sheep ovary: regulation of steroidogenic, haemodynamic and structural changes in the largest follicle and adjacent tissue before ovulation.
J. Reprod. Fertil. 45, 595–604.
|
CrossRef |
CAS |
PubMed |
Mueller, M. D., Lebovic, D. I., Garrett, E., and Taylor, R. N. (2000
).
Neutrophils infiltrating the endometrium express vascular endothelial growth factor: potential role in endometrial angiogenesis.
Fertil. Steril. 74, 107–112.
|
CrossRef |
CAS |
PubMed |
Murdoch, W. J. (1987
).
Treatment of sheep with prostaglandin F2 alpha enhances production of a luteal chemoattractant for eosinophils.
Am. J. Reprod. Immunol. Microbiol. 15, 52–56.
|
CAS |
PubMed |
Murdoch, W. J., Colgin, D. C., and Ellis, J. A. (1997
).
Role of tumor necrosis factor-alpha in the ovulatory mechanism of ewes.
J. Anim. Sci. 75, 1601–1605.
|
CAS |
PubMed |
Nagamatsu, T., and Schust, D. J. (2010
).
The contribution of macrophages to normal and pathological pregnancies.
Am. J. Reprod. Immunol. 63, 460–471.
|
CrossRef |
CAS |
PubMed |
Nasu, T., Maeshima, Y., Kinomura, M., Hirokoshi-Kawahara, K., Tanabe, K., Sugiyama, H., Sonoda, H., Sato, Y., and Makino, H. (2009
).
Vasohibin-1, a negative feedback regulator of angiogenesis, ameliorates renal alterations in a mouse model of diabetic nephropathy.
Diabetes 58, 2365–2375.
|
CrossRef |
CAS |
PubMed |
Nishimura, R., Bowolaksono, A., Acosta, T. J., Murakami, S., Piotrowska, K., Skarzynski, D. J., and Okuda, K. (2004
).
Possible role of interleukin-1 in the regulation of bovine corpus luteum throughout the luteal phase.
Biol. Reprod. 71, 1688–1693.
|
CrossRef |
CAS |
PubMed |
Niswender, G. D., Juengel, J. L., Silva, P. J., Rollyson, M. K., and McIntush, E. W. (2000
).
Mechanisms controlling the function and life span of the corpus luteum.
Physiol. Rev. 80, 1–29.
|
CAS |
PubMed |
Nitta, A., Shirasuna, K., Haneda, S., Matsui, M., Shimizu, T., Matsuyama, S., Kimura, K., Bollwein, H., and Miyamoto, A. (2011
).
Possible involvement of IFNT in lymphangiogenesis in the corpus luteum during the maternal recognition period in the cow.
Reproduction 142, 879–892.
|
CrossRef |
CAS |
PubMed |
Nozawa, H., Chiu, C., and Hanahan, D. (2006
).
Infiltrating neutrophils mediate the initial angiogenic switch in a mouse model of multistage carcinogenesis.
Proc. Natl Acad. Sci. USA 103, 12 493–12 498.
|
CrossRef |
CAS |
O’Reilly, M. S., Holmgren, L., Shing, Y., Chen, C., Rosenthal, R. A., Moses, M., Lane, W. S., Cao, Y., Sage, E. H., and Folkman, J. (1994
).
Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma.
Cell 79, 315–328.
|
CrossRef |
CAS |
PubMed |
O’Reilly, M. S., Boehm, T., Shing, Y., Fukai, N., Vasios, G., Lane, W. S., Flynn, E., Birkhead, J. R., Olsen, B. R., and Folkman, J. (1997
).
Endostatin: an endogenous inhibitor of angiogenesis and tumor growth.
Cell 88, 277–285.
|
CrossRef |
CAS |
PubMed |
Okuda, K., and Sakumoto, R. (2003
).
Multiple roles of TNF super family members in corpus luteum function.
Reprod. Biol. Endocrinol. 95, 1–10.
Otsuki, Y., Magari, S., and Sugimoto, O. (1986
).
Lymphatic capillaries in rabbit ovaries during ovulation: an ultrastructural study.
Lymphology 19, 55–64.
|
CAS |
PubMed |
Pate, J. L., and Landis Keyes, P. (2001
).
Immune cells in the corpus luteum: friends or foes?
Reproduction 122, 665–676.
|
CrossRef |
CAS |
PubMed |
Pate, J. L., Toyokawa, K., Walusimbi, S., and Brzezicka, E. (2010
).
The interface of the immune and reproductive systems in the ovary: lessons learned from the corpus luteum of domestic animal models.
Am. J. Reprod. Immunol. 64, 275–286.
|
CrossRef |
CAS |
PubMed |
Penny, L. A. (2000
).
Monocyte chemoattractant protein 1 in luteolysis.
Rev. Reprod. 5, 63–66.
|
CrossRef |
CAS |
PubMed |
Penny, L. A., Armstrong, D., Bramley, T. A., Webb, R., Collins, R. A., and Watson, E. D. (1999
).
Immune cells and cytokine production in the bovine corpus luteum throughout the oestrous cycle and after induced luteolysis.
J. Reprod. Fertil. 115, 87–96.
|
CrossRef |
CAS |
PubMed |
Petrovská, M., Dimitrov, D. G., and Michael, S. D. (1996
).
Quantitative changes in macrophage distribution in normal mouse ovary over the course of the estrous cycle examined with an image analysis system.
Am. J. Reprod. Immunol. 36, 175–183.
|
CrossRef |
PubMed |
Piccard, H., Muschel, R. J., and Opdenakker, G. (2011
).
On the dual roles and polarized phenotypes of neutrophils in tumor development and progression.
Crit. Rev. Oncol. Hematol. 82, 296–309.
|
PubMed |
Połeć, A., Tanbo, T., and Fedorcsak, P. (2009
).
Cellular interaction regulates interleukin-8 secretion by granulosa-lutein cells and monocytes/macrophages.
Am. J. Reprod. Immunol. 61, 85–94.
|
CrossRef |
PubMed |
Polec, A., Raki, M., Abyholm, T., Tanbo, T. G., and Fedorcsak, P. (2011
).
Interaction between granulosa-lutein cells and monocytes regulates secretion of angiogenic factors
in vitro.
Hum. Reprod. 26, 2819–2829.
|
CrossRef |
CAS |
PubMed |
Quigley, J. P., and Deryugina, E. I. (2012
).
Combating angiogenesis early: potential of targeting tumor-recruited neutrophils in cancer therapy.
Future Oncol. 8, 5–8.
|
CrossRef |
PubMed |
Robinson, R. S., Hammond, A. J., Mann, G. E., and Hunter, M. G. (2008
).
A novel physiological culture system that mimics luteal angiogenesis.
Reproduction 135, 405–413.
|
CrossRef |
CAS |
PubMed |
Rodgers, R. J., Mitchell, M. D., and Simpson, E. R. (1988
).
Secretion of progesterone and prostaglandins by cells of bovine corpora lutea from three stages of the luteal phase.
J. Endocrinol. 118, 121–126.
|
CrossRef |
CAS |
PubMed |
Sakurai, T., Suzuki, K., Yoshie, M., Hashimoto, K., Tachikawa, E., and Tamura, K. (2011
).
Stimulation of tube formation mediated through the prostaglandin EP
2 receptor in rat luteal endothelial cells.
J. Endocrinol. 209, 33–43.
|
CrossRef |
CAS |
PubMed |
Sales, K. J., List, T., Boddy, S. C., Williams, A. R., Anderson, R. A., Naor, Z., and Jabbour, H. N. (2005
).
A novel angiogenic role for prostaglandin F
2alpha–FP receptor interaction in human endometrial adenocarcinomas.
Cancer Res. 65, 7707–7716.
|
CAS |
PubMed |
Sato, Y. (2011
).
Is vasohibin-1 for more than angiogenesis inhibition?
J. Biochem. 149, 229–230.
|
CrossRef |
CAS |
PubMed |
Sato, Y., and Sonoda, H. (2007
).
The vasohibin family: a negative regulatory system of angiogenesis genetically programmed in endothelial cells.
Arterioscler. Thromb. Vasc. Biol. 27, 37–41.
|
CrossRef |
CAS |
PubMed |
Schledzewski, K., Falkowski, M., Moldenhauer, G., Metharom, P., Kzhyshkowska, J., Ganss, R., Demory, A., Falkowska-Hansen, B., Kurzen, H., Ugurel, S., Geginat, G., Arnold, B., and Goerdt, S. (2006
).
Lymphatic endothelium-specific hyaluronan receptor LYVE-1 is expressed by stabilin-1+, F4/80+, CD11b+ macrophages in malignant tumours and wound healing tissue
in vivo and in bone marrow cultures
in vitro: implications for the assessment of lymphangiogenesis.
J. Pathol. 209, 67–77.
|
CrossRef |
CAS |
PubMed |
Shen, L., Smith, J. M., Shen, Z., Eriksson, M., Sentman, C., and Wira, C. R. (2007
).
Inhibition of human neutrophil degranulation by transforming growth factor-beta1.
Clin. Exp. Immunol. 149, 155–161.
|
CrossRef |
CAS |
PubMed |
Shimizu, T., Kaji, A., Murayama, C., Magata, F., Shirasuna, K., Wakamiya, K., Okuda, K., and Miyamoto, A. (2012
).
Effects of interleukin-8 on estradiol and progesterone production by bovine granulosa cells from large follicles and progesterone production by luteinizing granulosa cells in culture.
Cytokine 57, 175–181.
|
CrossRef |
CAS |
PubMed |
Shirasuna, K., Sasahara, K., Matsui, M., Shimizu, T., and Miyamoto, A. (2010
).
Prostaglandin F
2alpha differentially affects mRNA expression relating to angiogenesis, vasoactivation and prostaglandins in the early and mid corpus luteum in the cow.
J. Reprod. Dev. 56, 428–436.
|
CrossRef |
CAS |
PubMed |
Shirasuna, K., Jiemtaweeboon, S., Raddatz, S., Nitta, A., Schuberth, H. J., Bollwein, H., Shimizu, T., and Miyamoto, A. (2012a
).
Rapid accumulation of polymorphonuclear neutrophils in the corpus luteum during prostaglandin F(2alpha)-induced luteolysis in the cow.
PLoS One 7, e29054.
|
CrossRef |
CAS |
PubMed |
Shirasuna, K., Kobayashi, A., Nitta, A., Nibuno, S., Sasahara, K., Shimizu, T., Bollwein, H., and Miyamoto, A. (2012b
).
Possible action of vasohibin-1 as an inhibitor in the regulation of vascularization of the bovine corpus luteum.
Reproduction 143, 491–500.
|
CrossRef |
CAS |
PubMed |
Short, R. E., Staigmiller, R. B., Bellows, R. A., and Ford, S. P. (1995
).
Endocrine responses in cows fed ponderosa pine needles and the effects of stress, corpus luteum regression, progestin, and ketoprofen.
J. Anim. Sci. 73, 198–205.
|
CAS |
PubMed |
Sica, A., Larghi, P., Mancino, A., Rubino, L., Porta, C., Totaro, M. G., Rimoldi, M., Biswas, S. K., Allavena, P., and Mantovani, A. (2008
).
Macrophage polarization in tumour progression.
Semin. Cancer Biol. 18, 349–355.
|
CrossRef |
CAS |
PubMed |
Singhal, P. C., Sankaran, R. T., Nahar, N., Shah, N., and Patel, P. (2000
).
Vasoactive agents modulate migration of monocytes across glomerular endothelial cells.
J. Investig. Med. 48, 110–117.
|
CAS |
PubMed |
Spencer, T. E., Burghardt, R. C., Johnson, G. A., and Bazer, F. W. (2004
).
Conceptus signals for establishment and maintenance of pregnancy.
Anim. Reprod. Sci. 82–83, 537–550.
|
CrossRef |
PubMed |
Standaert, F. E., Zamora, C. S., and Chew, B. P. (1991
).
Quantitative and qualitative changes in blood leukocytes in the porcine ovary.
Am. J. Reprod. Immunol. 25, 163–168.
|
CAS |
PubMed |
Tajima, T., Murata, T., Aritake, K., Urade, Y., Hirai, H., Nakamura, M., Ozaki, H., and Hori, M. (2008
).
Lipopolysaccharide induces macrophage migration via prostaglandin D(2) and prostaglandin E(2).
J. Pharmacol. Exp. Ther. 326, 493–501.
|
CrossRef |
CAS |
PubMed |
Tazzyman, S., Lewis, C. E., and Murdoch, C. (2009
).
Neutrophils: key mediators of tumour angiogenesis.
Int. J. Exp. Pathol. 90, 222–231.
|
CrossRef |
CAS |
PubMed |
Tombran-Tink, J., Chader, G. G., and Johnson, L. V. (1991
).
PEDF: a pigment epithelium-derived factor with potent neuronal differentiative activity.
Exp. Eye Res. 53, 411–414.
|
CrossRef |
CAS |
PubMed |
Townson, D. H., and Liptak, A. R. (2003
).
Chemokines in the corpus luteum: implications of leukocyte chemotaxis.
Reprod. Biol. Endocrinol. 1, 94.
|
CrossRef |
PubMed |
Townson, D. H., O’Connor, C. L., and Pru, J. K. (2002
).
Expression of monocyte chemoattractant protein-1 and distribution of immune cell populations in the bovine corpus luteum throughout the estrous cycle.
Biol. Reprod. 66, 361–366.
|
CrossRef |
CAS |
PubMed |
Turner, E. C., Hughes, J., Wilson, H., Clay, M., Mylonas, K. J., Kipari, T., Duncan, W. C., and Fraser, H. M. (2011
).
Conditional ablation of macrophages disrupts ovarian vasculature.
Reproduction 141, 821–831.
|
CrossRef |
CAS |
PubMed |
Wang, Y., and Oliver, G. (2010
).
Current views on the function of the lymphatic vasculature in health and disease.
Genes Dev. 24, 2115–2126.
|
CrossRef |
CAS |
PubMed |
Watanabe, K., Hasegawa, Y., Yamashita, H., Shimizu, K., Ding, Y., Abe, M., Ohta, H., Imagawa, K., Hojo, K., Maki, H., Sonoda, H., and Sato, Y. (2004
).
Vasohibin as an endothelium-derived negative feedback regulator of angiogenesis.
J. Clin. Invest. 114, 898–907.
|
CAS |
PubMed |
Xu, F., and Stouffer, R. L. (2009
).
Existence of the lymphatic system in the primate corpus luteum.
Lymphat. Res. Biol. 7, 159–168.
|
CrossRef |
CAS |
PubMed |
Yamada, Y., Nezu, J., Shimane, M., and Hirata, Y. (1997
).
Molecular cloning of a novel vascular endothelial growth factor, VEGF-D.
Genomics 42, 483–488.
|
CrossRef |
CAS |
PubMed |
Yamashita, H., Abe, M., Watanabe, K., Shimizu, K., Moriya, T., Sato, A., Satomi, S., Ohta, H., Sonoda, H., and Sato, Y. (2006
).
Vasohibin prevents arterial neointimal formation through angiogenesis inhibition.
Biochem. Biophys. Res. Commun. 345, 919–925.
|
CrossRef |
CAS |
PubMed |
Yasuda, M., Shimizu, S., Tokuyama, S., Watanabe, T., Kiuchi, Y., and Yamamoto, T. (2000
).
A novel effect of polymorphonuclear leukocytes in the facilitation of angiogenesis.
Life Sci. 66, 2113–2121.
|
CrossRef |
CAS |
PubMed |
Yoshinaga, K., Ito, K., Moriya, T., Nagase, S., Takano, T., Niikura, H., Yaegashi, N., and Sato, Y. (2008
).
Expression of vasohibin as a novel endothelium-derived angiogenesis inhibitor in endometrial cancer.
Cancer Sci. 99, 914–919.
|
CrossRef |
CAS |
PubMed |
Zarco, L., Stabenfeldt, G. H., Quirke, J. F., Kindahl, H., and Bradford, G. E. (1988
).
Release of prostaglandin F-2 alpha and the timing of events associated with luteolysis in ewes with oestrous cycles of different lengths.
J. Reprod. Fertil. 83, 517–526.
|
CrossRef |
CAS |
PubMed |
Zheng, J., Redmer, D. A., and Reynolds, L. P. (1993
).
Vascular development and heparin-binding growth factors in the bovine corpus luteum at several stages of the estrous cycle.
Biol. Reprod. 49, 1177–1189.
|
CrossRef |
CAS |
PubMed |
Zittermann, S. I., and Issekutz, A. C. (2006
).
Endothelial growth factors VEGF and bFGF differentially enhance monocyte and neutrophil recruitment to inflammation.
J. Leukoc. Biol. 80, 247–257.
|
CrossRef |
CAS |
PubMed |