AI Article Synopsis

  • Protein hydrolysate injection (PH) is a solution that contains hydrolyzed protein and sorbitol, comprising 17 amino acids, and has been studied for its effects on hematopoietic (blood-forming) function in models of cancer-induced damage.
  • PH was found to significantly increase the number of hematopoietic cells and restore blood cell concentrations in mice suffering from cyclophosphamide-induced myelosuppression, positively affecting various cell types and regulating key hematopoietic cytokines.
  • The study suggests that PH improves bone marrow function by regulating macrophage colony stimulating factor (M-CSF) expression, indicating its potential as a treatment for hematopoietic dysfunction resulting from cancer therapies.

Article Abstract

Protein hydrolysate injection (PH) is a sterile solution of hydrolyzed protein and sorbitol that contains 17 amino acids and has a molecular mass of 185.0-622.0 g/mol. This study investigated the effect of PH on hematopoietic function in K562 cells and mice with cyclophosphamide (CTX)-induced hematopoietic dysfunction. In these myelosuppressed mice, PH increased the number of hematopoietic cells in the bone marrow (BM) and regulated the concentration of several factors related to hematopoietic function. PH restored peripheral blood cell concentrations and increased the numbers of hematopoietic stem cells and progenitor cells (HSPCs), B lymphocytes, macrophages, and granulocytes in the BM of CTX-treated mice. Moreover, PH regulated the concentrations of macrophage colony stimulating factor (M-CSF), interleukin (IL)-2, and other hematopoiesis-related cytokines in the serum, spleen, femoral condyle, and sternum. In K562 cells, the PH-induced upregulation of hematopoiesis-related proteins was inhibited by transfection with M-CSF siRNA. Therefore, PH might benefit the BM hematopoietic system via the regulation of M-CSF expression, suggesting a potential role for PH in the treatment of hematopoietic dysfunction caused by cancer therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534652PMC
http://dx.doi.org/10.3390/cells10102776DOI Listing

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