Mice lacking histidine decarboxylase exhibit abnormal mast cells

Histidine decarboxylase (HDC) synthesizes histamine from histidine in mammals. To evaluate the role of histamine, we generated HDC-deficient mice using a gene targeting method. The mice showed a histamine deficiency and lacked histamine-synthesizing activity from histidine. These HDC-deficient mice...

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Published inFEBS letters Vol. 502; no. 1; pp. 53 - 56
Main Authors Ohtsu, Hiroshi, Tanaka, Satoshi, Terui, Tadashi, Hori, Yoshio, Makabe-Kobayashi, Yoko, Pejler, Gunnar, Tchougounova, Elena, Hellman, Lars, Gertsenstein, Marina, Hirasawa, Noriyasu, Sakurai, Eiko, Buzás, Edit, Kovács, Péter, Csaba, György, Kittel, Ágnes, Okada, Mikiko, Hara, Masahiro, Mar, Lynn, Numayama-Tsuruta, Keiko, Ishigaki-Suzuki, Satsuki, Ohuchi, Kazuo, Ichikawa, Atsushi, Falus, András, Watanabe, Takehiko, Nagy, András
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 27.07.2001
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Abstract Histidine decarboxylase (HDC) synthesizes histamine from histidine in mammals. To evaluate the role of histamine, we generated HDC-deficient mice using a gene targeting method. The mice showed a histamine deficiency and lacked histamine-synthesizing activity from histidine. These HDC-deficient mice are viable and fertile but exhibit a decrease in the numbers of mast cells while the remaining mast cells show an altered morphology and reduced granular content. The amounts of mast cell granular proteases were tremendously reduced. The HDC-deficient mice provide a unique and promising model for studying the role of histamine in a broad range of normal and disease processes.
AbstractList Histidine decarboxylase (HDC) synthesizes histamine from histidine in mammals. To evaluate the role of histamine, we generated HDC‐deficient mice using a gene targeting method. The mice showed a histamine deficiency and lacked histamine‐synthesizing activity from histidine. These HDC‐deficient mice are viable and fertile but exhibit a decrease in the numbers of mast cells while the remaining mast cells show an altered morphology and reduced granular content. The amounts of mast cell granular proteases were tremendously reduced. The HDC‐deficient mice provide a unique and promising model for studying the role of histamine in a broad range of normal and disease processes.
Author Falus, András
Buzás, Edit
Gertsenstein, Marina
Ishigaki-Suzuki, Satsuki
Ohuchi, Kazuo
Kovács, Péter
Csaba, György
Ohtsu, Hiroshi
Hara, Masahiro
Hori, Yoshio
Nagy, András
Tanaka, Satoshi
Okada, Mikiko
Numayama-Tsuruta, Keiko
Terui, Tadashi
Hellman, Lars
Hirasawa, Noriyasu
Watanabe, Takehiko
Pejler, Gunnar
Makabe-Kobayashi, Yoko
Mar, Lynn
Ichikawa, Atsushi
Kittel, Ágnes
Sakurai, Eiko
Tchougounova, Elena
Author_xml – sequence: 1
  givenname: Hiroshi
  surname: Ohtsu
  fullname: Ohtsu, Hiroshi
  email: ohtsu@mail.cc.tohoku.ac.jp
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 2
  givenname: Satoshi
  surname: Tanaka
  fullname: Tanaka, Satoshi
  organization: Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan
– sequence: 3
  givenname: Tadashi
  surname: Terui
  fullname: Terui, Tadashi
  organization: Department of Dermatology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 4
  givenname: Yoshio
  surname: Hori
  fullname: Hori, Yoshio
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 5
  givenname: Yoko
  surname: Makabe-Kobayashi
  fullname: Makabe-Kobayashi, Yoko
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 6
  givenname: Gunnar
  surname: Pejler
  fullname: Pejler, Gunnar
  organization: Department of Veterinary Medical Chemistry, Swedish University of Agricultural Sciences, BMC, P.O. Box 575, 751 23 Uppsala, Sweden
– sequence: 7
  givenname: Elena
  surname: Tchougounova
  fullname: Tchougounova, Elena
  organization: Department of Veterinary Medical Chemistry, Swedish University of Agricultural Sciences, BMC, P.O. Box 575, 751 23 Uppsala, Sweden
– sequence: 8
  givenname: Lars
  surname: Hellman
  fullname: Hellman, Lars
  organization: Department of Veterinary Medical Chemistry, Swedish University of Agricultural Sciences, BMC, P.O. Box 575, 751 23 Uppsala, Sweden
– sequence: 9
  givenname: Marina
  surname: Gertsenstein
  fullname: Gertsenstein, Marina
  organization: Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, ON, Canada M5G 1X5
– sequence: 10
  givenname: Noriyasu
  surname: Hirasawa
  fullname: Hirasawa, Noriyasu
  organization: Department of Pathophysiological Biochemistry, Faculty of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan
– sequence: 11
  givenname: Eiko
  surname: Sakurai
  fullname: Sakurai, Eiko
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 12
  givenname: Edit
  surname: Buzás
  fullname: Buzás, Edit
  organization: Department of Genetics, Cell- and Immunobiology, Semmelweis Medical University, 4 Nagyvárad tér, H-1089 Budapest, Hungary
– sequence: 13
  givenname: Péter
  surname: Kovács
  fullname: Kovács, Péter
  organization: Department of Genetics, Cell- and Immunobiology, Semmelweis Medical University, 4 Nagyvárad tér, H-1089 Budapest, Hungary
– sequence: 14
  givenname: György
  surname: Csaba
  fullname: Csaba, György
  organization: Department of Genetics, Cell- and Immunobiology, Semmelweis Medical University, 4 Nagyvárad tér, H-1089 Budapest, Hungary
– sequence: 15
  givenname: Ágnes
  surname: Kittel
  fullname: Kittel, Ágnes
  organization: Institute of Experimental Medicine, Budapest, Hungary
– sequence: 16
  givenname: Mikiko
  surname: Okada
  fullname: Okada, Mikiko
  organization: Department of Dermatology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 17
  givenname: Masahiro
  surname: Hara
  fullname: Hara, Masahiro
  organization: Department of Dermatology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 18
  givenname: Lynn
  surname: Mar
  fullname: Mar, Lynn
  organization: Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, ON, Canada M5G 1X5
– sequence: 19
  givenname: Keiko
  surname: Numayama-Tsuruta
  fullname: Numayama-Tsuruta, Keiko
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 20
  givenname: Satsuki
  surname: Ishigaki-Suzuki
  fullname: Ishigaki-Suzuki, Satsuki
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 21
  givenname: Kazuo
  surname: Ohuchi
  fullname: Ohuchi, Kazuo
  organization: Department of Pathophysiological Biochemistry, Faculty of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan
– sequence: 22
  givenname: Atsushi
  surname: Ichikawa
  fullname: Ichikawa, Atsushi
  organization: Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan
– sequence: 23
  givenname: András
  surname: Falus
  fullname: Falus, András
  organization: Department of Genetics, Cell- and Immunobiology, Semmelweis Medical University, 4 Nagyvárad tér, H-1089 Budapest, Hungary
– sequence: 24
  givenname: Takehiko
  surname: Watanabe
  fullname: Watanabe, Takehiko
  organization: Department of Cellular Pharmacology, Tohoku University School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan
– sequence: 25
  givenname: András
  surname: Nagy
  fullname: Nagy, András
  email: nagy@mshri.on.ca
  organization: Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, ON, Canada M5G 1X5
BackLink https://www.ncbi.nlm.nih.gov/pubmed/11478947$$D View this record in MEDLINE/PubMed
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10.1093/nar/28.14.2627
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ContentType Journal Article
Copyright 2001 Federation of European Biochemical Societies
FEBS Letters 502 (2001) 1873-3468 © 2015 Federation of European Biochemical Societies
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Issue 1
Keywords MC-CPA, mast cell carboxypeptidase A
Histamine
α-FMH, α-fluoromethyl histidine
Mast cell
HDC, histidine decarboxylase
MMCP, mouse mast cell protease
Rodent
BMMC, bone marrow-derived mast cell
Knockout
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Snippet Histidine decarboxylase (HDC) synthesizes histamine from histidine in mammals. To evaluate the role of histamine, we generated HDC-deficient mice using a gene...
Histidine decarboxylase (HDC) synthesizes histamine from histidine in mammals. To evaluate the role of histamine, we generated HDC‐deficient mice using a gene...
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SubjectTerms Alleles
Animals
BMMC, bone marrow-derived mast cell
HDC, histidine decarboxylase
Histamine
Histamine - biosynthesis
Histamine - metabolism
Histidine Decarboxylase - genetics
Histidine Decarboxylase - physiology
Knockout
Mast cell
Mast Cells - cytology
MC-CPA, mast cell carboxypeptidase A
Mice
Mice, Knockout
MMCP, mouse mast cell protease
Rodent
α-FMH, α-fluoromethyl histidine
Title Mice lacking histidine decarboxylase exhibit abnormal mast cells
URI https://dx.doi.org/10.1016/S0014-5793(01)02663-1
https://onlinelibrary.wiley.com/doi/abs/10.1016%2FS0014-5793%2801%2902663-1
https://www.ncbi.nlm.nih.gov/pubmed/11478947
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