Insulin-like growth factor binding protein-5 (IGFBP-5) is a key molecule in mammary gland development, which facilitates the removal of mammary epithelial cells (MECs) by apoptosis that takes place during remodeling of the mammary gland during involution. IGFBP-5 binds with IGFs for their bioavailabiliiy. IGFBP-5 has been reported to perform pleiotropic roles such as cellular apoptosis, proliferation and differentiation. To understand the role of IGFBP-5 during lactation and clinical mastitis, expression profiling of IGFBP-5 at the protein level was performed in both indigenous cows (Bos indicus) and buffaloes (Bubalus bubalis) belonging to two different breeds Sahiwal cows and Murrah buffaloes. Reverse-transcriptase PCR (RT-PCR) of IGFBP-5 mRNA confirmed its expression in milk somatic cells and MECs of Sahiwal cows. ELISA was performed for quantitative measurement of IGFBP-5 concentrations in milk during different days (0, 50, 100, 150, 200, 250 and 300) of lactation, during the involution period and in animals exhibiting short lactation and clinical mastitis. The highest concentration of IGFBP-5 in milk was observed during the involution period followed by colostrum, late and early lactation, respectively, in both cattle and buffaloes. No significant difference in the concentration of IGFBP-5 was observed during the first 150 days of lactation between cows and buffaloes. However, higher concentration of IGFBP-5 was observed in cows during late lactation (200 to 300 days) in comparison with buffaloes. To validate the ELISA data, quantitative real-time PCR was performed in MECs of Sahiwal cows. The relative mRNA abundance of IGFBP-5 was found to be significantly (P <0.05) higher on day 15 than between 50 and 150 days of lactation in case of Sahiwal cows. Highest mRNA expression of IGFBP-5 was observed around 300 days of lactation followed by 200 and 250 days (P <0.05), respectively. Murrah buffaloes showed low levels of IGFBP-5 protein in milk as compared with Sahiwal cows during lactation in ELISA. Animals having history of short lactation length (short lactating animals) showed higher levels of IGFBP-5 expression (at protein level) in comparison with normal lactating animals. We propose that higher level IGFBP-5 expression may have functional significance in lactation persistency. As a pro-apoptotic molecule, higher expression of IGFBP-5 was observed to be inversely related to lactation length and milk production.
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Univ Arkansas Med Sci, Dept Pathol, Winthrop P Rockefeller Canc Inst, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Dept Pathol, Winthrop P Rockefeller Canc Inst, Little Rock, AR 72205 USA
Johnson, Sarah K.
Haun, Randy S.
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Univ Arkansas Med Sci, Dept Pathol, Winthrop P Rockefeller Canc Inst, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Dept Pathol, Winthrop P Rockefeller Canc Inst, Little Rock, AR 72205 USA
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Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Taipei City Hosp, Dept Med Res & Educ, Taipei, Taiwan
Taipei Vet Gen Hosp, Dept Stomatol, Taipei, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Chang, Kuo-Wei
Hung, Pei-Shih
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Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Hung, Pei-Shih
Lin, I-Ying
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Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Lin, I-Ying
Hou, Chung-Ping
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Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Hou, Chung-Ping
Chen, Li-Kai
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Taipei City Hosp, Dept Dent, Taipei, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Chen, Li-Kai
Tsai, Yin-Meng
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Natl Yang Ming Univ, Inst Tradit Med, Taipei 112, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Tsai, Yin-Meng
Lin, Shu-Chun
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Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
Taipei City Hosp, Dept Med Res & Educ, Taipei, Taiwan
Taipei Vet Gen Hosp, Dept Stomatol, Taipei, TaiwanNatl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei 112, Taiwan
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Cent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R ChinaCent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R China
Sun, Min
Long, Juan
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Cent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R ChinaCent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R China
Long, Juan
Yi, Yuxin
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Cent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R ChinaCent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R China
Yi, Yuxin
Xia, Wei
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Univ Michigan, Dept Dermatol, Room 6447,Med Sci 1,1301 Catherine St, Ann Arbor, MI 48105 USACent S Univ, Xiangya Hosp, Dept Dermatol, Changsha, Hunan, Peoples R China
机构:
Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Chan, Dessy
Zhou, Yuanyuan
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Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Zhou, Yuanyuan
Chui, Chung Hin
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Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Chui, Chung Hin
Lam, Kim Hung
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Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Lam, Kim Hung
Law, Simon
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Univ Hong Kong, Li Ka Shing Fac Med, Dept Surg, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Law, Simon
Chan, Albert Sun-chi
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Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Chan, Albert Sun-chi
Li, Xingshu
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Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Li, Xingshu
Lam, Alfred King-yin
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Griffith Univ, Griffith Med Sch, Gold Coast, Qld 4222, AustraliaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China
Lam, Alfred King-yin
Tang, Johnny Cheuk On
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Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Dept Appl Biol & Chem Technol, State Key Lab Chem Biol & Drug Discovery, Hong Kong, Hong Kong, Peoples R China