CREBZF Antibody (OAAF06262)
- Known as:
- CREBZF Antibody (OAAF06262)
- Catalog number:
- oaaf06262
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Aviva Systems Biology
- Gene target:
- CREBZF Antibody (OAAF06262)
Related genes to: CREBZF Antibody (OAAF06262)
- Gene:
- CREBZF NIH gene
- Name:
- CREB/ATF bZIP transcription factor
- Previous symbol:
- -
- Synonyms:
- ZF
- Chromosome:
- 11q14.1
- Locus Type:
- gene with protein product
- Date approved:
- 2006-11-13
- Date modifiied:
- 2014-11-19
Related products to: CREBZF Antibody (OAAF06262)
Related articles to: CREBZF Antibody (OAAF06262)
- Ovarian secretion of steroid hormones is crucial for female reproductive health. CREBZF, a basic leucine zipper transcription factor, can heterodimerize with other transcription factors to regulate genes involved in various biological processes. This study investigates the role of CREBZF in female reproduction and steroid hormone synthesis regulation. Whole ovarian knockout of CREBZF affects the estrous cycle, antral follicle development, and testosterone and estradiol levels in female mice. Conditional knockout of CREBZF in Cyp17a1-positive cells results in altered serum testosterone during estrus, impaired postpartum maternal behavior, and significantly reduced offspring survival, associated with abnormal corticosterone and oxytocin levels. In NCI-H295R cells induced for steroidogenesis, CREBZF knockdown reduced testosterone and corticosterone secretion. RNA sequencing of CREBZF-knockdown NCI-H295R cells identified 51 differentially expressed genes enriched in steroidogenesis-related pathways. CREBZF knockdown also reduced c-Jun and ApoE expression, with a significant decrease in intracellular cholesterol. CREBZF interacts with c-Jun and binds to the ApoE promoter to regulate expression. Database screening identified two CREBZF/c-Jun binding sites, where CREBZF enhances c-Jun-mediated activation of ApoE at Site1 ( 299 to 286 bp), but inhibits it at Site2 (+70 to +83 bp). In conclusion, the CREBZF/c-Jun complex regulates ApoE expression, influencing cholesterol levels and female steroidogenesis, which is crucial for reproductive function. - Source: PubMed
Niu Hong-YuLi ChaoZhang Rui-HangDu Mu-ZiWuen Ji-YaLiu Hao-KunLi Zu-HuiWang Ai-HuaJin Ya-PingLin Peng-Fei - Osteoarthritis (OA) is a degenerative joint disease caused by the breakdown of joint cartilage and adjacent bone. Joint injury, being overweight, differences in leg length, high levels of joint stress, abnormal joint or limb development, and inherited factors have been implicated in the etiology of OA. In addition to physical damage to the joint, a role for inflammatory processes has been identified as well. Small heterodimer partner-interacting leucine zipper protein (SMILE) regulates transcription and many cellular functions. Among the proteins activated by SMILE is the peroxisome proliferator-activated receptor (PPAR) γ, which mediates the activities of CD4 + T helper cells, including Th1, Th2, and Th17, as well as Treg cells. PPAR-γ binds to STAT3 to inhibit its transcription, thereby suppressing the expression of the NF-κB pathway, and in turn, the expression of the inflammatory cytokines interferon (IFN), interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α, which are sub-signals of STAT3 and NF-κB. - Source: PubMed
Publication date: 2024/11/12
Moon JeonghyeonCho Keun-HyungJhun JooYeonChoi JeongWonNa Hyun-SikLee Jeong SuLee Seung YoonMin Jun-KiShetty AnanPark Sung-HwanKim Seok JungCho Mi-La - Quantum dots have diverse biomedical applications, from constructing biological infrastructures like medical imaging to advancing pharmaceutical research. However, concerns about human health arise due to the toxic potential of quantum dots based on heavy metals. Therefore, research on quantum dots has predominantly focused on oxidative stress, cell death, and other broader bodily toxicities. This study investigated the toxicity and cellular responses of mouse embryonic stem cells (mESCs) and mouse adult stem cells (mASCs) to nitrogen-doped carbon quantum dots (NCQDs) made of non-metallic materials. Cells were exposed to NCQDs, and we utilized a fluorescent ubiquitination-based cell system to verify whether NCQDs induce cytotoxicity. Furthermore, we validated the differentiation-inducing impact of NCQDs by utilizing embryonic stem cells equipped with the Oct4 enhancer-GFP reporter system. By analyzing gene expression including Crebzf, Chop, and ATF6, we also observed that NCQDs robustly elicited endoplasmic reticulum (ER) stress. We confirmed that NCQDs induced cytotoxicity and abnormal differentiation. Interestingly, we also confirmed that low concentrations of NCQDs stimulated cell proliferation in both mESCs and mASCs. In conclusion, NCQDs modulate cell death, proliferation, and differentiation in a concentration-dependent manner. Indiscriminate biological applications of NCQDs have the potential to cause cancer development by affecting normal cell division or to fail to induce normal differentiation by affecting embryonic development during pregnancy. Therefore, we propose that future biomedical applications of NCQDs necessitate comprehensive and diverse biological studies. - Source: PubMed
Publication date: 2024/10/02
Song Hyun HeeChoi HyunwooKim SeonghanKim Hwan GyuAn SangminKim SejungJang Hoon - The global challenge of male infertility is escalating, notably due to the decreased testosterone (T) synthesis in testicular Leydig cells under stress, underscoring the critical need for a more profound understanding of its regulatory mechanisms. CREBZF, a novel basic region-leucine zipper transcription factor, regulates testosterone synthesis in mouse Leydig cells in vitro; however, further validation through in vivo experiments is essential. Our study utilized Cyp17a1-Cre to knock out CREBZF in androgen-synthesis cells and explored the physiological roles of CREBZF in fertility, steroid hormone synthesis, and behaviors in adult male mice. Conditional knockout (cKO) CREBZF did not affect fertility and serum testosterone level in male mice. Primary Leydig cells isolated from CREBZF-cKO mice showed impaired testosterone secretion and decreased mRNA levels of Star, Cyp17a1, and Hsd3b1. Loss of CREBZF resulted in thickening of the adrenal cortex, especially X-zone, with elevated serum corticosterone and dehydroepiandrosterone levels and decreased serum dehydroepiandrosterone sulfate levels. Immunohistochemical staining revealed increased expression of StAR, Cyp11a1, and 17β-Hsd3 in the adrenal cortex of CREBZF-cKO mice, while the expression of AR was significantly reduced. Along with the histological changes and abnormal steroid levels in the adrenal gland, CREBZF-cKO mice showed higher anxiety-like behavior and impaired memory in the elevated plus maze and Barnes maze, respectively. In summary, CREBZF is dispensable for fertility, and CREBZF deficiency in Leydig cells promotes adrenal function in adult male mice. These results shed light on the requirement of CREBZF for fertility, adrenal steroid synthesis, and stress response in adult male mice, and contribute to understanding the crosstalk between testes and adrenal glands. - Source: PubMed
Niu HongyuLi ChaoZhang HexinLiu HaokunShang ChunmeiJia YanniWuenjiya Li ZuhuiWang AihuaJin YapingLin Pengfei - Glucose is required for generating heat during cold-induced nonshivering thermogenesis in adipose tissue, but the regulatory mechanism is largely unknown. CREBZF has emerged as a critical mechanism for metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD). We investigated the roles of CREBZF in the control of thermogenesis and energy metabolism. Glucose induces CREBZF in human white adipose tissue (WAT) and inguinal WAT (iWAT) in mice. Lys208 acetylation modulated by transacetylase CREB-binding protein/p300 and deacetylase HDAC3 is required for glucose-induced reduction of proteasomal degradation and augmentation of protein stability of CREBZF. Glucose induces rectal temperature and thermogenesis in white adipose of control mice, which is further potentiated in adipose-specific CREBZF knockout (CREBZF FKO) mice. During cold exposure, CREBZF FKO mice display enhanced thermogenic gene expression, browning of iWAT, and adaptive thermogenesis. CREBZF associates with PGC-1α to repress thermogenic gene expression. Expression levels of CREBZF are negatively correlated with UCP1 in human adipose tissues and increased in WAT of obese ob/ob mice, which may underscore the potential role of CREBZF in the development of compromised thermogenic capability under hyperglycemic conditions. Our results reveal an important mechanism of glucose sensing and thermogenic inactivation through reversible acetylation. - Source: PubMed
Publication date: 2024/04/08
Cui AoyuanXue YaqianSu WeitongLin JingLiu YuxiaoCai GenxiangWan QinJiang YangDing DongZheng ZengpengWei ShuangLi WenjingShen JiaxinWen JianHuang MengyaoZhao JiuxiangZhang XiaojieZhao YuwuLi HongYing HaoZhang HaibingBi YanChen YanXu AiminXu YongLi Yu