Unravelling the Role of Apoptosis in Platelets Biogenesis Through the Study of the Thrombocytopenia THC4

NCT07026578 | Active Not Recruiting

• 1 other identifier: THC4
• Study Type: observational
• Target: 38
• Locations: 1 country
• Sites: 1

Brief Summary

Inherited thrombocytopenias (ITs) are disorders characterized by a reduced platelet count, caused by variants in at least 40 genes. Mutations in CYCS cause a rare autosomal-dominant IT, named Thrombocytopenia 4 (THC4). The CYCS gene encodes cytochrome C (CytC), a small heme protein localized in mitochondria. It functions as an electron carrier in the respiratory chain as well as one of the main actors of the intrinsic pathway of apoptosis. Although THC4 is the only disease associated with CYCS mutations, its clinical and molecular features are still poorly characterized. Moreover, pathogenesis of THC4 is still unclear. In vitro studies demonstrated that CYCS mutations exert a proapoptotic activity and enhanced peroxidase activity, as well as affect the mitochondrial respiratory function in yeast. The role of apoptosis in platelet biogenesis is a highly controversial issue. Some studies suggested that megakaryocytes must undergo apoptosis to promote platelet release. In fact, mice carrying mutations impairing apoptosis exhibited thrombocytopenia and pharmacological inhibition of caspases blocked platelet production, supporting this hypothesis. Conversely, investigations on mice genetically modified for the BCL-2 family proteins, initiators of apoptosis, concluded that megakaryocytes must restrain apoptosis in order to generate platelets. Since thrombocytopenia is the only phenotypic manifestation of CYCS mutations, the investigators believe that THC4 represents a unique model for deciphering the role of Cytc and apoptosis in megakaryopoiesis and platelet biogenesis. Preliminary data: The applicant unit is a reference center for ITs. The database includes 375 families; among these, 7 presented with mutations in CYCS gene, accounting for 26 THC4 patients. Patients presented mild thrombocytopenia, normal mean platelet volume and morphology, without hematological or extra-hematological defects. The investigators isolated platelets and hematopoietic progenitors from peripheral blood of 9 patients. Platelets were analyzed under baseline conditions; a part was treated with an inducer of apoptosis (ABT-737). Surprisingly, the expression of cytC was found reduced in platelets of all analyzed patients. Platelets showed no signs of early death. Instead, when stimulated with ABT-737, they showed inability to undergo apoptosis, suggesting that CYCS mutations confer resistance to apoptosis. Hematopoietic progenitors from 3 patients were differentiated in megakaryocytes. Maturation and differentiation were comparable between THC4 and healthy controls. Instead, their capability to form proplatelets was profoundly defective. These preliminary data suggest that CytC deficit could be associated with inability to form proplatelets in THC4 megakaryocytes, and that this defect underlies thrombocytopenia, supporting the crucial role of cytC in platelet production.

Conditions

Thrombocytopenia, Isolated; Thrombocytopenia 4; CYCS MUTATION- ASSOCIATED THROMBOCYTOPENIA THC4

Keywords

Apoptosis; Platelet biogenesis; Thrombocytopenia 4

Outcome Measures

Primary Outcomes (1)

• Pathogenetic CYCS variants result in defective Cytc expression

  The primary outcome of the study is to demonstrate that mutations in CYCS results in reduction of the expression of Cytochrome C in THC4 platelets. The primary endpoint will compare Cytochrome C expression in platelets between THC4 patients and healthy controls. This will be assessed by measuring Cytochrome C protein levels in platelet lysates collected from both groups. Western blotting will be used to quantify the amount of Cytochrome C protein.

  The primary endpoint measurement will be performed immediately after the enrollment (baseline).

Secondary Outcomes (1)

• The impact of Cytochrome C (CytC) deficiency on apoptotic mechanisms evaluated as the comparison of the apoptotic markers between CYCS-silenced cells and cells transduced with the vector alone

  The production of in vitro models and execution of tests to evaluate the apoptotic profile will take 2 weeks

Other Outcomes (1)

• The effects of alterations of apoptotic mechanisms on megakaryopoiesis and platelet production evaluated as a decrease in CD61+ and CD42b+ cells and reduced ability to form proplatelets in vitro

  Along with the measurement of Cytochrome C in platelets, circulating progenitors will be collected from patients, from which megakaryocytes will be differentiated in vitro, either immediately upon enrollment (baseline)

Study Arms (2)

CYCS mutated

Procedure: Blood draw for the laboratory assessment

healthy controls

Procedure: Blood draw for the laboratory assessment

Interventions

Blood draw for the laboratory assessment PROCEDURE

This is an observational study . The procedures will be carried out in according to clinical practice

CYCS mutated; healthy controls

Eligibility Criteria

• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

All subjects with suspected Inherited Thrombocytopenia (IT) observed at the SC Medicina generale 1, Fondazione IRCCS Policlinico San Matteo

You may qualify if:

• Molecular diagnosis of THC4, through the identification of a pathogenic variant of the CYCS gene
• Acquisition of written informed consent

Sponsors & Collaborators

• Fondazione IRCCS Policlinico San Matteo di Pavia: lead

Study Sites (1)

SC Medicina Generale 1, Fondazione IRCCS Policlinico San Matteo

Pavia, Pavia, 27100, Italy

Location

Biospecimen

Retention: SAMPLES WITH DNA

25 mL of peripheral whole blood anticoagulated with ACD for platelet isolation and for separation of hematopoietic progenitors to differentiate megakaryocytes

MeSH Terms

Conditions

Thrombocytopenia; Thrombocytopenia 4

Interventions

Blood Specimen Collection

Condition Hierarchy (Ancestors)

Blood Platelet Disorders; Hematologic Diseases; Hemic and Lymphatic Diseases; Cytopenia

Intervention Hierarchy (Ancestors)

Specimen Handling; Clinical Laboratory Techniques; Diagnostic Techniques and Procedures; Diagnosis; Punctures; Surgical Procedures, Operative; Investigative Techniques

Study Design

• Study Type: observational
• Observational Model: CASE CONTROL
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Biologist

Study Record Dates

• First Submitted: March 13, 2025
• First Posted: June 18, 2025
• Study Start: June 18, 2024
• Primary Completion (Estimated): June 30, 2026
• Study Completion (Estimated): June 30, 2026
• Last Updated: June 18, 2025

Record last verified: 2025-04

Locations

IT (1)