Thromb Haemost 1995; 74(06): 1516-1520
DOI: 10.1055/s-0038-1649975
Original Articles
Fibrinolysis
Schattauer GmbH Stuttgart

Cultured Human Mesangial Cells Produce both Type 1 and Type 2 Plasminogen Activator Inhibitors

Mario Colucci
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Loreto Gesualdo
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Pasqualina Montemurro
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Luca G Cavallo
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Massimo Conese
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Elisa Mascolo
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Elena Ranieri
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Salvatore Di Paolo
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Francesco P Schena
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
,
Nicola Semeraro
The Dipartimento di Scienze Biomediche e Oncologia Umana Sezione di Patologia Generate, and Cattedra di Nefrologia, Universita di Bari, Bari, Italy
› Author Affiliations
Further Information

Publication History

Received 19 July 1994

Accepted after resubmission 06 September 1995

Publication Date:
10 July 2018 (online)

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Summary

Cultured human mesangial cells (HMC) derived from normal kidneys have been shown to synthesize tissue-type plasminogen activator (t-PA) and excess amounts of PA inhibitor type 1 (PAI-1). Conflicting results have been obtained concerning the production of urokinase-type PA (u-PA) and efforts to show PA inhibitor 2 (PAI-2) met with failure. We evaluated the fibrinolytic profile of cultured HMC lines obtained from 12 patients with renal carcinoma and one cadaveric kidney donor. Subconfluent cells (third passage) were incubated overnight in serum-free medium. t-PA, u-PA, PAI-1 and PAI-2 antigens were assayed by ELISA methods and PA and PAI activities by amidolytic methods both in conditioned medium (CM) and cell extracts (CE). Besides PAI-1, PAI-2 antigen was detected in all but one HMC lines. At variance with the former, which was largely released in the culture medium, PAI-2 was mainly cell-associated. t-PA antigen was found in all but two cell lines while u-PA antigen was detected in relatively high concentrations in 8 cell lines. PA activity, identified as u-PA by functional and immunological criteria, was measured in CM of six of the eight u-PA producing cell lines, whereas PAI activity was undetectable or very low in CM of all cell lines, suggesting that PAI-1 was largely inactive. Functional assays of cell extracts demonstrated the presence of PA activity, again identified as u-PA, only in samples (five lines) containing u-PA antigen in excess over PAI-2. PAI activity was found instead in the extracts in which the inhibitor was higher than the activator (six lines) and was identified as PAI-2, as it inhibited u-PA but not single-chain t-PA and was neutralized by a polyclonal anti-PAI-2 antibody. The heterogeneous fibrinolytic pattern of HMC lines was confirmed by mRNA analysis of three representative lines. Results were similar when HMC lines at passage five were used, except that the u-PA content was significantly reduced both in CM and CE. These findings indicate that the fibrinolytic profile of cultured HMC is more complex than previously reported. The production of large amounts of PAI-2 may represent an additional control mechanism of proteinase activity.

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