Thymus and Activation Regulated Chemokine (CCL17) Rhesus Macaque Recombinant produced in E.Coli is a non-glycosylated polypeptide chain containing 71 amino acid and having a molecular mass of approximately 8.1kDa.
TRAC is purified by proprietary chromatographic techniques.
The TARC cDNA encodes a precursor protein consisting of 94 amino acids, including a 23 amino acid signal peptide. This signal peptide is cleaved to yield the mature secreted protein, which comprises 71 amino acids. Belonging to the CC chemokine family, CCL-17 shares approximately 24-29% amino acid sequence identity with other chemokines like RANTES, MIP-1a, MIP-1b, MCP-1, MCP-2, MCP-3, and I-309. TARC expression is primarily observed in the thymus, with lower levels detected in the lung, colon, and small intestine. Additionally, transient expression is observed in stimulated peripheral blood mononuclear cells. Recombinant TARC exhibits chemotactic activity towards T cell lines but not monocytes or neutrophils. CCL-17 specifically binds to CCR4, a receptor selectively expressed on T cells. As one of the few Cys-Cys (CC) cytokine genes located on chromosome 16's q arm, CCL17 displays chemotactic activity for T lymphocytes but not monocytes or granulocytes. CCL17 interacts with chemokine receptors CCR4 and CCR8, playing a crucial role in T cell development within the thymus and the trafficking and activation of mature T cells.
Recombinant Thymus and Activation Regulated Chemokine (CCL17) from Rhesus Macaque, produced in E. coli, is a non-glycosylated polypeptide chain consisting of 71 amino acids. It has a molecular weight of approximately 8.1 kDa. The purification of TRAC is achieved using proprietary chromatographic methods.
Sterile Filtered White lyophilized (freeze-dried) powder.
Lyophilized from a 0.2 µm filtered solution in 20mM PB, 0.02% Tween-20 and 300mM NaCl, at a pH of 7.4.
To reconstitute the lyophilized Thymus and Activation Regulated Chemokine Rhesus Macaque, it is recommended to dissolve it in sterile 18 MΩ-cm H2O to a concentration of at least 100 µg/ml. This solution can be further diluted in other aqueous solutions as needed.
Lyophilized TRAC remains stable at room temperature for up to 3 weeks. However, for long-term storage, it is recommended to store it desiccated below -18°C. Once reconstituted, Thymus and Activation Regulated Chemokine Rhesus Macaque should be stored at 4°C for 2-7 days. For future use, store below -18°C. Avoid repeated freeze-thaw cycles.
The purity is determined to be greater than 97.0% using the following methods:
(a) RP-HPLC analysis.
(b) SDS-PAGE analysis.
C-C motif chemokine 17, Small-inducible cytokine A17, Thymus and activation-regulated chemokine, CC chemokine TARC, ABCD-2, CCL17, CCL-17, SCYA17, TARC, A-152E5.3, MGC138271, MGC138273.
Escherichia Coli.
ARGTNVGREC CLKYFKGAIP LRKLKTWYQT SEDCSRDAIV FVTVQNKAIC SDPNDKKVKK ALKYLQSLER S.
TARC (Thymus and Activation-Regulated Chemokine, also known as CCL17) is a chemokine protein identified in macaques. According to molecular characterization, macaque TARC is a single non-glycosylated polypeptide chain containing 71 amino acids with the sequence: ARGTNVGREC CLKYFKGAIP LRKLKTWYQT SEDCSRDAIV FVTVQNKAIC SDPNDKKVKK ALKYLQSLER S . This protein demonstrates biological activity primarily through chemotaxis of T-lymphocytes at concentration ranges of 1.0-10 ng/ml . TARC appears to function as a signaling molecule within the immune system, though its full range of functions in macaques is still being investigated. Recent research suggests potential roles in auditory thalamocortical circuits as well .
Macaque models provide valuable insights into TARC-related immune responses due to their physiological similarity to humans. To effectively utilize these models, researchers should:
Select appropriate macaque species based on research questions (options include rhesus macaques, Barbary macaques, crested macaques, and Moor macaques)
Implement proper tissue collection and preservation protocols for optimal protein integrity
Utilize consistent methodologies for TARC quantification across studies
Account for age, sex, and environmental factors that may influence TARC expression
When designing studies, researchers should consider that macaque TARC demonstrates chemotactic activity for T-lymphocytes, suggesting its involvement in immune cell recruitment and inflammatory pathways .
For optimal isolation and quantification of TARC in macaque samples, researchers should implement the following methodological approach:
For recombinant protein production, E. coli expression systems have been successfully employed to generate biologically active macaque TARC with endotoxin levels below 0.1 EU/μg .
When designing behavioral studies with macaques, researchers must consider their complex social organization. Macaque societies are matriarchal, with females typically remaining in the same troupe throughout their lives while males experience continuous turnover . This social structure influences research design in several ways:
Female macaques reach reproductive maturity at approximately five years, coinciding with the typical "retirement" period of dominant males (5-6 years), which naturally prevents inbreeding
Observers should account for hierarchical relationships, as dominant males receive grooming from lower-ranking males who adopt submissive postures in their presence
Researchers should note that macaques engage in daily "socializing" activities to maintain group bonding
As troupes grow larger, relationships may become more distant, potentially leading to subgroup formation and troupe splitting
These social dynamics are crucial considerations when designing behavioral studies, particularly those examining TARC expression in relation to stress, immune function, or social factors.
Recent advanced modeling of macaque auditory thalamocortical circuits provides insights into potential relationships between TARC expression and neural activity. A detailed model incorporating primary auditory cortex (A1), medial geniculate body (MGB), and thalamic reticular nucleus has been developed using the NEURON simulator and NetPyNE tool . This model simulates:
A cortical column with over 12,000 neurons and 25 million synapses
Cell-type-specific neuron densities, morphology, and connectivity across six cortical layers
Reciprocal connections between A1 and MGB thalamus
Interneurons and core/matrix-layer-specific projections to A1
The model successfully reproduces physiological firing rates, local field potentials (LFPs), current source densities (CSDs), and electroencephalography (EEG) signals comparable to in vivo recordings . While specific TARC expression patterns within these circuits require further investigation, this model provides a quantitative theoretical framework for integrating experimental data on TARC's potential role in auditory processing.
Translating macaque TARC research to human applications presents several methodological challenges:
Species-specific protein differences: Despite similarities, macaque TARC may differ from human TARC in structure and function, necessitating careful cross-species validation
Experimental design limitations: The controlled environments of laboratory studies may not fully replicate the complexity of human immune responses in real-world settings
Ethical considerations: According to research on macaque-human interactions, 87.6% of survey respondents felt that conserving and protecting macaques is important, highlighting the need for ethical research practices
Data interpretation complexities: Physiological oscillations that emerge spontaneously across frequency bands in macaque models must be carefully analyzed to determine relevance to human systems
Researchers addressing these challenges should implement cross-validation strategies and consider both the unique aspects of macaque biology and the ethical implications of their research approaches.
Human-macaque interactions create complex research scenarios that may affect TARC expression through stress responses and environmental factors. Field studies have documented patterns of interaction that researchers should consider:
Interaction Type | Percentage | Research Implications |
---|---|---|
Affiliative/submissive behaviors | 46.9% | Potential stress reduction effects |
Aggression | 19.1% | Possible acute stress responses |
Taking food/items | 18.5% | Dietary and pathogen exposure variables |
Searching bins/cars/houses | 13.4% | Environmental contaminant exposure |
Nonaggressive contact | 2.1% | Potential zoonotic transmission opportunities |
Importantly, most interactions (two-thirds) occurred when humans carried food or food cues, while one-quarter happened when humans provoked macaques. Only 8% of interactions lacked a clear human-triggered context . These patterns suggest human behavior significantly influences macaque behavior, potentially altering physiological responses including TARC expression.
Ethical field research with macaques requires balancing scientific objectives with animal welfare and community perspectives. Survey data reveals that:
Nearly half of respondents held neutral attitudes toward macaques
Only 26.2% believed conflict with macaques warranted urgent action
Nearly two-thirds supported education programs to reduce human-macaque conflict
Less than 15% supported removing or eradicating macaques
87.6% considered macaque conservation and protection important
Based on these findings, researchers should:
Implement non-invasive sampling techniques whenever possible
Engage local communities in research planning and execution
Incorporate educational components into research programs
Design studies that minimize disruption to natural behaviors
Consider differences between resident and visitor perceptions, as residents reported more nuisance problems and held more negative sentiments toward macaques
When analyzing TARC expression data in macaque populations, researchers should consider several statistical approaches based on study design:
For longitudinal studies: Mixed-effects models to account for repeated measures and individual variation
For comparative studies across groups: ANOVA or non-parametric alternatives with appropriate post-hoc tests
For correlational analyses: Multivariate models that control for age, sex, social rank, and environmental factors
For network analyses: Graph theoretical approaches to examine relationships between TARC expression and neural circuit activity
Data from macaque auditory thalamocortical studies demonstrate the emergence of physiological oscillations across frequency bands comparable to in vivo recordings . These complex data sets require sophisticated analytical approaches to disentangle population-specific contributions to observed oscillation events and relate them to firing and presynaptic input patterns.
When confronting contradictory findings in TARC function across macaque species, researchers should implement a systematic analytical framework:
Examine methodological differences: Variation in sample collection, processing, and analysis techniques may explain apparent contradictions
Consider species-specific adaptations: Different macaque species (rhesus, Barbary, crested, Moor) may exhibit evolutionary adaptations in TARC function related to their ecological niches
Evaluate contextual factors: Housing conditions, social structure, and environmental factors may influence TARC expression and function
Assess developmental timing: Age-related changes in TARC expression may vary across species
Compare social organization impacts: Matriarchal social structures with female kinship bonds may create species-specific patterns of immune function
A comprehensive meta-analysis approach, with standardized effect size calculations and formal heterogeneity assessments, provides the most robust method for reconciling contradictory findings.
Several cutting-edge technologies offer significant potential for advancing macaque TARC research:
Single-cell RNA sequencing: Enables high-resolution mapping of TARC expression across cell populations
CRISPR-Cas9 gene editing: Allows precise manipulation of TARC-related pathways in macaque models
Advanced computational modeling: Building on existing multiscale models of macaque neural circuits , future simulations could incorporate TARC signaling pathways
Non-invasive imaging techniques: Advanced methods for visualizing TARC expression in living macaques
Artificial intelligence approaches: Machine learning algorithms for identifying patterns in complex TARC expression data
These technologies, when combined with traditional methods, will enable researchers to address complex questions about TARC's role in macaque physiology and behavior.
Environmental stressors from climate change and habitat loss may significantly impact TARC expression in wild macaque populations through multiple pathways:
Altered immune challenges: Changing pathogen distributions and exposure patterns
Nutritional stress: Reduced food availability affecting immune function
Increased human-macaque conflict: As habitats shrink, increased human interaction may alter stress responses
Population density effects: Compressed habitats may increase intraspecies competition and stress
Thermal stress responses: Direct physiological effects of temperature changes
Conservation research indicates that macaque species worldwide face significant threats from habitat loss, climate change, and growing human populations . Future studies should examine how these environmental changes influence TARC expression and related immune functions in wild populations, potentially integrating approaches from the University of Portsmouth Macaque Project, which has established research with wild crested and Moor macaques in Sulawesi, Indonesia .
Thymus and Activation Regulated Chemokine (TARC), also known as CCL17, is a member of the CC chemokine family. It plays a crucial role in the immune system by attracting T cells to sites of inflammation and infection. The recombinant form of CCL17 from Rhesus Macaque is produced using advanced biotechnological methods, often involving expression in E. coli.
CCL17 is involved in the chemotaxis of T-helper cells, particularly type 2 helper T cells (Th2), cutaneous lymphocyte skin-localizing T cells, and regulatory T cells . It mediates its effects by binding to the CCR4 receptor, which is expressed on these cells . This interaction is crucial for the immune response, as it helps direct T cells to sites where they are needed to combat infections or inflammation.
Elevated levels of CCL17 have been associated with various eosinophilic disorders, including allergic asthma and atopic dermatitis . The chemokine’s role in these conditions highlights its importance in type 2 immune responses. Additionally, CCL17 has been linked to cancer, where it can either aid in immune evasion by attracting regulatory T cells or improve outcomes in certain cancers like melanoma .
Recombinant CCL17 from Rhesus Macaque is used in research to study its role in immune responses and its potential therapeutic applications. By understanding how CCL17 functions, scientists can develop new treatments for diseases involving the immune system, such as autoimmune disorders, allergies, and cancer.