Effects of oral β‐cryptoxanthin administration on the transcriptomes of peripheral neutrophil and liver tissue using microarray analysis in post‐weaned Holstein calves.

Autor: Kimura, Atsushi, Kim, Yo‐Han, Hashizume, Kazuyoshi, Ito, Akira, Mukai, Katsuyuki, Kizaki, Keiichiro, Sato, Shigeru
Předmět:
Zdroj: Journal of Animal Physiology & Animal Nutrition; Sep2023, Vol. 107 Issue 5, p1167-1175, 9p
Abstrakt: We investigated the effects of oral administration of β‐cryptoxanthin (β‐CRX), a precursor of vitamin A synthesis, on the transcriptomes of peripheral neutrophils and liver tissue in post‐weaned Holstein calves with immature immunity. A single oral administration of β‐CRX (0.2 mg/kg body weight) was performed in eight Holstein calves (4.0 ± 0.8 months of age; 117 ± 10 kg) on Day 0. Peripheral neutrophils (n = 4) and liver tissue (n = 4) were collected on Days 0 and 7. Neutrophils were isolated by density gradient centrifugation and treated with the TRIzol reagent. mRNA expression profiles were examined by microarray and differentially expressed genes were investigated using the Ingenuity Pathway Analysis software. The differentially expressed candidate genes identified in neutrophils (COL3A1, DCN, and CCL2) and liver tissue (ACTA1) were involved in enhanced bacterial killing and maintenance of cellular homoeostasis respectively. The changes in the expression of six of the eight common genes encoding enzymes (ADH5 and SQLE) and transcription regulators (RARRES1, COBLL1, RTKN, and HES1) were in the same direction in neutrophils and liver tissue. ADH5 and SQLE are involved in the maintenance of cellular homoeostasis by increasing the availability of substrates, and RARRES1, COBLL1, RTKN, and HES1 are associated with the suppression of apoptosis and carcinogenesis. An in silico analysis revealed that MYC, which is related to the regulation of cellular differentiation and apoptosis, was the most significant upstream regulator in neutrophils and liver tissue. Transcription regulators such as CDKN2A (cell growth suppressor) and SP1 (cell apoptosis enhancer) were significantly inhibited and activated, respectively, in neutrophils and liver tissue. These results suggest that oral administration of β‐CRX promotes the expression of candidate genes related to bactericidal ability and regulation of cellular processes in peripheral neutrophils and liver cells in response to the immune‐enhancing function of β‐CRX in post‐weaned Holstein calves. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
Externí odkaz: